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Based on this guide's real question bank — 201 practice questions across 8 units. Slide to match your situation.
Unit 1: Chemistry of Life
▾Properties of water
- Polarity: O is more electronegative than H → bent molecule with partial negative O and partial positive H's → forms hydrogen bonds between molecules
- Cohesion: water molecules stick to each other via H-bonds → surface tension, allows water columns to move up xylem
- Adhesion: water sticks to other polar surfaces → capillary action (water climbing a thin glass tube or plant cell walls)
- High specific heat (1 cal/g°C): H-bonds absorb/release large amounts of heat with small temperature change → moderates climate and organism body temperature
- Universal solvent: polar/charged solutes dissolve readily; ions become surrounded by water (hydration shells)
- Density anomaly: ice is LESS dense than liquid water (H-bonds lock into a fixed hexagonal lattice) → ice floats, insulating water below
Macromolecules & functional groups
- Carbohydrates: monomer = monosaccharide (glucose, fructose); function = energy storage (starch, glycogen) and structure (cellulose, chitin)
- Lipids: not true polymers; glycerol + 3 fatty acids = triglyceride; function = long-term energy storage, membranes (phospholipids), hormones (steroids)
- Proteins: monomer = amino acid (20 types), joined by peptide bonds; function = enzymes, structure, transport, signaling, defense
- Nucleic acids: monomer = nucleotide (sugar+phosphate+nitrogenous base); DNA stores genetic info, RNA involved in gene expression
- Dehydration synthesis (condensation): monomers join, releasing one H₂O per bond formed
- Hydrolysis: polymer broken into monomers by ADDING a water molecule across each bond (digestion uses hydrolysis)
Functional groups
- Hydroxyl (-OH): polar, found in sugars and alcohols; enables hydrogen bonding, increases solubility
- Carboxyl (-COOH): acidic, found in amino acids and fatty acids; can donate H⁺ (ionizes to -COO⁻)
- Amino (-NH₂): basic, found in amino acids; can accept H⁺ (ionizes to -NH₃⁺)
- Phosphate (-PO₄): found in nucleotides, ATP, phospholipids; negatively charged, involved in energy transfer
- Methyl (-CH₃): nonpolar, affects gene expression via DNA methylation, affects molecular shape
Protein structure
- Primary structure: linear sequence of amino acids, determined by the gene's codon sequence; held by peptide bonds
- Secondary structure: local folding into α-helices and β-pleated sheets, stabilized by hydrogen bonds between backbone atoms
- Tertiary structure: overall 3D shape of one polypeptide, driven by R-group interactions (hydrophobic interactions, ionic bonds, hydrogen bonds, disulfide bridges)
- Quaternary structure: two or more polypeptide subunits joined (e.g., hemoglobin = 4 subunits)
- Denaturation: heat, pH change, or salt disrupts weak bonds → protein unfolds and loses function (primary structure usually intact)
Enzymes & activation energy
- Activation energy (Ea): the energy barrier that must be overcome to start a reaction; enzymes lower Ea without changing ΔG (they don't change whether a reaction is spontaneous)
- Active site: region of the enzyme where substrate binds; induced fit model — enzyme shape adjusts slightly around substrate for optimal fit
- Enzymes are substrate-specific due to active site shape; each enzyme typically catalyzes one reaction or reaction type
- Competitive inhibitor: binds the active site itself, blocking substrate; effect reduced by increasing substrate concentration
- Noncompetitive (allosteric) inhibitor: binds a site other than the active site, changes enzyme shape so active site no longer works well; not overcome by more substrate
- Enzyme activity affected by temperature (optimum, then denatures above it) and pH (each enzyme has an optimal pH range, e.g. pepsin ~2, trypsin ~8)
Dehydration synthesis: releases H₂O | Hydrolysis: adds H₂O
Unit 2: Cell Structure & Function
▾Prokaryotic vs eukaryotic cells
- Prokaryotes (bacteria, archaea): no nucleus, DNA is a single circular chromosome in the nucleoid region, no membrane-bound organelles, smaller (1-10 μm), 70S ribosomes
- Eukaryotes (protists, fungi, plants, animals): true membrane-bound nucleus, linear DNA wound around histones, membrane-bound organelles, larger (10-100 μm), 80S ribosomes
- Both have: plasma membrane, cytoplasm, ribosomes, DNA as genetic material
- Surface area-to-volume ratio limits cell size: as a cell grows, volume increases faster (cubed) than surface area (squared) → limits nutrient/waste exchange rate → cells divide or fold membranes rather than grow indefinitely
Endosymbiotic theory
- Evidence: mitochondria and chloroplasts have their own circular DNA (like bacteria), their own 70S ribosomes, and double membranes (inner = original bacterial membrane, outer = from engulfing vesicle)
- Both organelles replicate independently of the cell cycle by binary fission, similar to bacteria
- Mitochondria likely derived from an aerobic heterotrophic bacterium; chloroplasts from a photosynthetic cyanobacterium
- This theory explains why these organelles are semi-autonomous within eukaryotic cells
Organelles & their functions
- Nucleus: houses DNA, site of transcription and DNA replication; nucleolus makes ribosomal RNA/subunits
- Rough ER: ribosomes attached, synthesizes and folds membrane/secreted proteins; Smooth ER: lipid synthesis, detoxification, calcium storage
- Golgi apparatus: modifies, sorts, and packages proteins/lipids received from the ER (cis face receives, trans face ships)
- Mitochondria: site of aerobic cellular respiration, produces most cellular ATP; cristae increase inner membrane surface area
- Lysosome (animal cells): contains hydrolytic enzymes for digesting macromolecules, worn-out organelles (autophagy), and pathogens
- Chloroplast (plant cells): site of photosynthesis; central vacuole (plants): storage, maintains turgor pressure, waste storage
Membrane structure
- Phospholipid bilayer: hydrophilic phosphate heads face the aqueous environments (inside/outside); hydrophobic fatty acid tails face each other in the middle
- 'Fluid': phospholipids and proteins move laterally within the layer; fluidity increases with unsaturated fatty acids (kinks prevent tight packing) and decreases with cholesterol at high temps (buffers fluidity in both directions)
- 'Mosaic': many different proteins embedded at varying depths — integral (span the membrane) vs peripheral (attached to surface)
- Membrane proteins function as: channels/transporters, receptors, cell recognition markers (glycoproteins), enzymes, and cell junction anchors
Membrane transport & osmosis
- Simple diffusion: small/nonpolar molecules (O₂, CO₂) move directly through the bilayer down their concentration gradient
- Facilitated diffusion: polar molecules/ions move through channel or carrier proteins down their gradient — still passive, no ATP
- Active transport: moves solutes AGAINST their gradient, requires ATP (e.g., sodium-potassium pump moves 3 Na⁺ out, 2 K⁺ in per ATP)
- Osmosis: diffusion of water across a selectively permeable membrane, from low solute (high water potential) to high solute (low water potential) concentration
- Hypotonic solution (lower solute outside): water enters cell → animal cells lyse, plant cells become turgid (healthy)
- Hypertonic solution (higher solute outside): water leaves cell → animal cells crenate/shrivel, plant cells plasmolyze
Na⁺/K⁺ pump: 3 Na⁺ out, 2 K⁺ in per ATP
Unit 3: Cellular Energetics
▾ATP & energy coupling
- ATP → ADP + Pi releases ~7.3 kcal/mol; this exergonic reaction is coupled to endergonic cellular work (active transport, synthesis, mechanical work)
- ATP is regenerated from ADP + Pi using energy released from cellular respiration (phosphorylation)
- Energy coupling: the phosphate group is often transferred directly to a substrate (phosphorylation), providing energy and changing substrate shape/reactivity
Cellular respiration overview
- Glycolysis (cytoplasm, anaerobic): glucose (6C) split into 2 pyruvate (3C); net gain 2 ATP (substrate-level phosphorylation) + 2 NADH
- Pyruvate oxidation (mitochondrial matrix): each pyruvate → acetyl-CoA + CO₂ + NADH (occurs twice per glucose)
- Krebs/citric acid cycle (matrix): acetyl-CoA oxidized completely to CO₂; produces per glucose (2 turns): 6 NADH, 2 FADH₂, 2 ATP
- Electron transport chain (inner mitochondrial membrane): NADH/FADH₂ donate electrons, which pass down the chain pumping H⁺ into intermembrane space, creating a gradient; O₂ is the final electron acceptor, forming H₂O
- Chemiosmosis: H⁺ flows back through ATP synthase down its gradient, driving ATP synthesis (oxidative phosphorylation) — the majority of ATP (~26-28 of ~30-32 total) is made here
- Total ATP yield per glucose: approximately 30-32 ATP (varies by shuttle system efficiency)
Fermentation
- Purpose of fermentation: regenerate NAD⁺ (needed for glycolysis step 6) when O₂ is unavailable — only glycolysis's 2 ATP are produced (no Krebs or ETC)
- Lactic acid fermentation: pyruvate → lactate directly (occurs in muscle cells during intense exercise, some bacteria/yogurt)
- Alcoholic fermentation: pyruvate → acetaldehyde + CO₂ → ethanol (occurs in yeast; used in brewing, baking)
- Anaerobic respiration (different from fermentation) uses an ETC but with a final electron acceptor other than O₂ (e.g., sulfate) — some prokaryotes only
Photosynthesis: light reactions
- Photosystem II (P680) absorbs light, excites electrons, which pass down an ETC to Photosystem I, pumping H⁺ into the thylakoid lumen (chemiosmosis, like mitochondria)
- Water is split (photolysis) to replace electrons lost from PS II: 2H₂O → 4H⁺ + 4e⁻ + O₂ (this is the source of the O₂ released by photosynthesis)
- Photosystem I (P700) re-excites electrons, which are passed to NADP⁺ + H⁺ → NADPH (via ferredoxin and NADP⁺ reductase)
- ATP synthase uses the H⁺ gradient (lumen high, stroma low) to produce ATP via chemiosmosis — same mechanism as in mitochondria
- Products of light reactions (ATP and NADPH) are used to power the Calvin cycle; O₂ is released as a byproduct
Photosynthesis: Calvin cycle
- Carbon fixation: CO₂ is attached to RuBP (5C) by the enzyme rubisco, forming an unstable 6C compound that splits into two 3-PG (3C) molecules
- Reduction: ATP and NADPH (from light reactions) convert 3-PG into G3P (glyceraldehyde-3-phosphate)
- Regeneration: most G3P molecules are used to regenerate RuBP (using more ATP) so the cycle continues; 1 out of every 6 G3P produced (net, after 3 turns) exits to build glucose
- 3 turns of the cycle (fixing 3 CO₂) use 9 ATP and 6 NADPH to net one G3P, which can combine with another G3P to form one glucose
≈30–32 ATP per glucose (aerobic respiration total)
Calvin cycle: 3 CO₂ + 9 ATP + 6 NADPH → 1 G3P (net)
Unit 4: Cell Communication & Cell Cycle
▾Signal transduction pathways
- Reception: a signaling molecule (ligand) binds a specific receptor protein, either on the cell surface (for polar/large ligands) or inside the cell (for lipid-soluble/nonpolar ligands like steroid hormones)
- Transduction: receptor activation triggers a cascade of molecular changes, often via a series of relay proteins — a common mechanism is a phosphorylation cascade (kinases add phosphate groups, activating the next protein in line)
- Second messengers (e.g., cyclic AMP, Ca²⁺) amplify the signal — one receptor activation can trigger production of many second messenger molecules, amplifying the response manyfold
- Response: the pathway ultimately alters cell behavior — activating/deactivating enzymes, changing gene expression, altering cytoskeleton, or opening ion channels
- G-protein coupled receptors: ligand binding activates a G protein, which activates an effector enzyme (e.g., adenylyl cyclase making cAMP)
Cell cycle phases
- Interphase: G1 (cell growth, organelle production) → S (DNA replication, chromosomes become sister chromatids) → G2 (further growth, prep for division); interphase makes up ~90% of the cycle
- Mitosis stages: prophase (chromosomes condense, spindle forms) → metaphase (chromosomes align at metaphase plate) → anaphase (sister chromatids separate, pulled to opposite poles) → telophase (nuclear envelopes reform, chromosomes decondense)
- Cytokinesis: division of the cytoplasm — animal cells pinch via a cleavage furrow (actin ring); plant cells build a cell plate that becomes a new cell wall
- G0 phase: non-dividing state that many differentiated cells (e.g., neurons) enter permanently, or temporarily until a signal triggers re-entry into G1
Cell cycle regulation
- G1 checkpoint (restriction point): checks cell size, nutrients, and DNA integrity — the main 'go/no-go' point; without a go-ahead signal, cell enters G0
- G2 checkpoint: verifies DNA replication completed correctly and without damage before entering mitosis
- M checkpoint (spindle assembly checkpoint): verifies all chromosomes are properly attached to spindle fibers before anaphase begins
- Cyclins bind and activate CDKs; cyclin levels rise and fall through the cycle, while CDK levels stay constant — together (cyclin-CDK complexes, e.g., MPF) they phosphorylate target proteins to trigger the next phase
Cancer & apoptosis
- Proto-oncogenes: normal genes that promote cell division; a gain-of-function mutation turns them into oncogenes that overstimulate division (act like a stuck accelerator)
- Tumor suppressor genes (e.g., p53, RB): normally inhibit cell division or trigger apoptosis when DNA is damaged; loss-of-function mutations remove this brake
- p53 ('guardian of the genome'): detects DNA damage, halts the cell cycle for repair, or triggers apoptosis if damage is irreparable; mutated in over half of human cancers
- Apoptosis: programmed cell death — a controlled process that removes damaged, infected, or unneeded cells without releasing harmful contents into surrounding tissue (unlike necrosis)
- Metastasis: cancer cells lose contact inhibition and anchorage dependence, invade nearby tissue, and can spread to distant sites via blood/lymph
Cyclin + CDK → active complex → drives phase transition
Unit 5: Heredity
▾Meiosis
- Meiosis I (reductional division): homologous chromosomes separate — prophase I includes synapsis (homologs pair up) and crossing over (exchange of genetic material between non-sister chromatids), a major source of genetic variation
- Independent assortment: homologous pairs align randomly at the metaphase I plate, so maternal/paternal chromosomes sort into gametes independently — for n chromosome pairs, 2ⁿ possible combinations
- Meiosis II (equational division, like mitosis): sister chromatids separate — produces 4 haploid (n) cells from the 2 cells made in meiosis I
- Sources of genetic variation: crossing over (prophase I), independent assortment (metaphase I), and random fertilization (any sperm can fertilize any egg)
- Nondisjunction: failure of chromosomes/chromatids to separate properly → gametes with abnormal chromosome numbers (e.g., trisomy 21/Down syndrome from an extra chromosome 21)
Mendelian genetics
- Law of segregation: the two alleles for a gene separate during meiosis so each gamete gets only one allele
- Law of independent assortment: alleles of different genes (on different chromosomes) assort independently into gametes
- Genotype: the allele combination (e.g., Bb); Phenotype: the observable trait (e.g., brown eyes) resulting from genotype and environment
- Homozygous: two identical alleles (BB or bb); Heterozygous: two different alleles (Bb)
- Complete dominance: heterozygote shows only the dominant phenotype (Bb looks like BB)
Monohybrid & dihybrid crosses
- Monohybrid cross (one gene): Bb × Bb → offspring ratio 1 BB : 2 Bb : 1 bb genotypically → 3:1 dominant:recessive phenotypically
- Test cross: cross an unknown-genotype dominant phenotype individual with a homozygous recessive to reveal whether it's homozygous or heterozygous dominant
- Dihybrid cross (two independently assorting genes): AaBb × AaBb → 9:3:3:1 phenotypic ratio (assuming independent assortment and no linkage)
- Multiplication rule: for independent events (e.g., two separate gene crosses), multiply individual probabilities to get the combined probability
Non-Mendelian inheritance
- Incomplete dominance: heterozygote phenotype is a BLENDED intermediate of both alleles (e.g., red × white snapdragon → pink; RR:Rr:rr gives 1:2:1 ratio phenotypically too)
- Codominance: heterozygote shows BOTH parental phenotypes fully and simultaneously, not blended (e.g., AB blood type shows both A and B antigens; roan cattle with both red and white hairs)
- Multiple alleles: more than 2 alleles exist for a gene in the population (e.g., ABO blood type has IA, IB, i alleles; only 2 present in any individual)
- Sex-linked inheritance: genes on the X chromosome show different inheritance in males (XY, only one X allele expressed, hemizygous) vs females (XX) — e.g., red-green color blindness, hemophilia are X-linked recessive and more common in males
- Linked genes: genes located close together on the same chromosome tend to be inherited together, violating independent assortment unless separated by crossing over (closer genes = less recombination)
- Polygenic traits: controlled by multiple genes with additive effects, producing continuous variation (e.g., human height, skin color)
Monohybrid ratio (Aa × Aa): 3:1 (phenotype), 1:2:1 (genotype)
2ⁿ = number of possible gamete combinations (n = # of chromosome pairs)
Unit 6: Gene Expression & Regulation
▾DNA replication
- Helicase unwinds and unzips the double helix at the origin of replication, creating a replication fork
- DNA polymerase adds new nucleotides only in the 5'→3' direction, reading the template strand 3'→5'
- Leading strand: synthesized continuously toward the replication fork; Lagging strand: synthesized discontinuously away from the fork in Okazaki fragments, later joined by DNA ligase
- Primase lays down a short RNA primer to give DNA polymerase a starting 3'-OH group; primers are later replaced with DNA
- DNA polymerase also proofreads, removing mismatched nucleotides — high fidelity replication with a very low error rate
Central dogma: transcription & translation
- Transcription (in the nucleus of eukaryotes): RNA polymerase uses one DNA strand as a template to synthesize a complementary mRNA strand (5'→3'); in eukaryotes, pre-mRNA is processed — 5' cap and poly-A tail added, introns spliced out leaving only exons
- Translation (at ribosomes): mRNA codons (3-nucleotide sequences) are read in the ribosome; tRNA molecules, each carrying a specific amino acid and complementary anticodon, pair with codons
- Ribosome moves along mRNA, and peptide bonds form between amino acids, building a polypeptide chain until a stop codon is reached
- Genetic code is degenerate (redundant, multiple codons can code for the same amino acid) but unambiguous (each codon specifies only one amino acid) and nearly universal across all life
- Start codon AUG codes for methionine and sets the reading frame; stop codons (UAA, UAG, UGA) terminate translation without coding for an amino acid
Mutations
- Point mutation (substitution): one base is changed — silent (codes for same amino acid, no effect), missense (codes for different amino acid), or nonsense (creates a premature stop codon)
- Frameshift mutation (insertion or deletion of bases not in multiples of 3): shifts the reading frame downstream of the mutation, usually causing a completely different, often nonfunctional protein
- Insertions/deletions in multiples of 3 add/remove whole amino acids but don't shift the frame
- Mutations in somatic cells affect only that organism (not heritable); mutations in germ-line cells (gametes) can be passed to offspring
- Mutagens (UV light, chemicals, radiation) increase mutation rate; mutations are also the ultimate source of all new genetic variation for natural selection
Gene regulation
- Lac operon (inducible, prokaryotic): in the absence of lactose, a repressor binds the operator, blocking transcription of lactose-digesting genes; when lactose is present, it binds the repressor, removing it from the operator, allowing transcription
- Trp operon (repressible, prokaryotic): normally 'on'; when tryptophan is abundant, it acts as a co-repressor, activating the repressor to bind the operator and shut off transcription (negative feedback)
- Eukaryotic gene regulation occurs at multiple levels: chromatin structure (heterochromatin = tightly packed/inactive vs euchromatin = loosely packed/active), transcription (transcription factors, enhancers/promoters), post-transcriptional (alternative splicing, mRNA stability), and post-translational (protein modification/degradation)
- Epigenetics: heritable changes in gene expression without changing DNA sequence — DNA methylation (usually silences genes) and histone acetylation (usually activates genes by loosening chromatin)
Biotechnology basics
- PCR (polymerase chain reaction): amplifies a specific DNA sequence exponentially using primers, DNA polymerase (Taq), and repeated cycles of denaturation (heat separates strands), annealing (primers bind), and extension (polymerase synthesizes new strand)
- Gel electrophoresis: separates DNA fragments by size using an electric field — DNA is negatively charged (phosphate backbone) and migrates toward the positive electrode; smaller fragments move farther/faster through the gel matrix
- Restriction enzymes cut DNA at specific recognition sequences, producing fragments (often with 'sticky ends') used in cloning and creating restriction fragment patterns for comparison
- Recombinant DNA/genetic engineering: a gene of interest is inserted into a plasmid vector (using the same restriction enzyme to create complementary sticky ends) and introduced into a host cell (e.g., bacteria producing human insulin)
PCR cycle: denature → anneal → extend
DNA charge: negative (moves toward + electrode in electrophoresis)
Unit 7: Natural Selection
▾Evidence for evolution
- Fossil record: shows a chronological sequence of changing life forms and transitional forms between major groups
- Comparative anatomy: homologous structures (same underlying structure, different function, e.g., forelimbs of humans/whales/bats) indicate common ancestry; analogous structures (different origin, similar function, e.g., wings of insects and birds) indicate convergent evolution, not common ancestry
- Vestigial structures: reduced, functionless remnants of structures that were functional in an ancestor (e.g., human appendix, whale pelvic bones)
- Molecular biology: the more similar the DNA/protein sequences (e.g., cytochrome c) between two species, the more recently they likely shared a common ancestor
- Biogeography: geographic distribution of species reflects evolutionary history and geological events (e.g., continental drift, island colonization)
Hardy-Weinberg equilibrium
- p + q = 1 (allele frequencies for a 2-allele gene: p = dominant allele frequency, q = recessive allele frequency)
- p² + 2pq + q² = 1 (genotype frequencies: p² = homozygous dominant, 2pq = heterozygous, q² = homozygous recessive)
- Five conditions required for equilibrium (no evolution): no mutation, no gene flow (migration), infinitely large population (no genetic drift), random mating, and no natural selection
- If observed genotype frequencies differ significantly from Hardy-Weinberg predictions, one or more of these conditions is being violated, and the population is evolving
Mechanisms of evolution
- Natural selection: individuals with heritable traits better suited to the environment survive and reproduce at higher rates, increasing the frequency of favorable alleles
- Genetic drift: random change in allele frequencies, with a larger effect in SMALL populations; bottleneck effect (population sharply reduced by a random event) and founder effect (small group establishes a new isolated population) are two types
- Gene flow (migration): movement of alleles between populations via migrating individuals, tends to reduce genetic differences between populations
- Types of selection: directional (favors one phenotypic extreme, shifts the mean), stabilizing (favors the intermediate phenotype, reduces variation, e.g., human birth weight), disruptive (favors both extremes over the intermediate, can increase variation/lead to speciation)
- Sexual selection: a form of natural selection based on differential mating success — can produce traits that don't obviously aid survival (e.g., peacock tails)
Speciation & phylogenetics
- Reproductive isolation prevents gene flow between populations, allowing them to diverge into separate species; mechanisms are prezygotic (prevent mating/fertilization, e.g., habitat, temporal, behavioral, mechanical, gametic isolation) or postzygotic (hybrid inviability, hybrid sterility, e.g., mules)
- Allopatric speciation: geographic separation (e.g., river, mountain range) prevents gene flow, populations diverge independently — the most common mode of speciation
- Sympatric speciation: new species arises without geographic separation, often via polyploidy (especially common in plants), habitat differentiation, or sexual selection
- Phylogenetic trees/cladograms: branching diagrams showing hypothesized evolutionary relationships; a shared derived character (synapomorphy) defines a clade; the node represents the most recent common ancestor of the branches above it
- More shared derived characteristics = more closely related; outgroup comparison helps root a tree and determine the direction of character change
p² + 2pq + q² = 1
q² = frequency of homozygous recessive genotype → q = √(q²)
Unit 8: Ecology
▾Population growth models
- Exponential growth (J-curve): occurs with unlimited resources; rate of increase is proportional to population size; dN/dt = rN
- Logistic growth (S-curve): growth slows as population approaches carrying capacity (K) due to density-dependent limiting factors; dN/dt = rN(K−N)/K
- Carrying capacity (K): the maximum population size an environment can sustainably support given its resources
- Density-dependent limiting factors: intensify as population density increases (competition for food/space, predation, disease, waste accumulation)
- Density-independent limiting factors: affect population regardless of density (natural disasters, extreme weather, habitat destruction)
- r-selected species: many small offspring, little parental care, fast maturation, thrive in unstable/exponential-growth conditions (insects, weeds); K-selected species: fewer offspring, more parental investment, thrive near carrying capacity (elephants, humans)
Community interactions
- Competition (−/−): both species harmed when using the same limited resource; competitive exclusion principle states two species cannot indefinitely occupy the exact same niche
- Predation (+/−): predator benefits, prey is harmed/killed; can drive coevolutionary 'arms races' (e.g., cheetah speed vs gazelle speed)
- Mutualism (+/+): both species benefit (e.g., mycorrhizae fungi and plant roots, gut bacteria and humans)
- Commensalism (+/0): one species benefits, the other is unaffected (e.g., barnacles on a whale)
- Parasitism (+/−): parasite benefits at the host's expense, usually without immediately killing the host
- Resource partitioning: species divide a limited resource by using different parts of it (niche differentiation), reducing direct competition
Ecosystem energy flow
- Producers (autotrophs, e.g., plants, algae, cyanobacteria) convert solar energy into chemical energy via photosynthesis, forming the base of the food chain
- Primary consumers (herbivores) eat producers; secondary consumers (carnivores) eat primary consumers; tertiary consumers eat secondary consumers
- Only about 10% of energy is transferred from one trophic level to the next (the rest is lost as heat via cellular respiration, or is unused/undigested) — the 10% rule
- Trophic pyramid: energy, biomass, and typically numbers all decrease at higher trophic levels, limiting food chain length (usually 4-5 levels)
- Gross primary productivity (GPP): total energy captured by producers; Net primary productivity (NPP) = GPP − energy producers use for their own respiration
Biogeochemical cycles
- Carbon cycle: CO₂ fixed by photosynthesis into organic carbon, returned to atmosphere via cellular respiration, decomposition, and combustion; also stored long-term in fossil fuels and dissolved in oceans
- Nitrogen cycle: atmospheric N₂ is largely unusable by most organisms until nitrogen-fixing bacteria (e.g., Rhizobium in legume root nodules) convert it to ammonia/ammonium; nitrification converts this to nitrite then nitrate (usable by plants); denitrification returns N₂ to the atmosphere
- Phosphorus cycle: has no significant atmospheric component — phosphorus cycles mainly through rock weathering, soil, water, and living organisms (a key component of DNA, ATP, phospholipids)
- Water cycle: driven by solar energy — evaporation/transpiration, condensation, precipitation, and runoff/infiltration
Climate & biodiversity
- Biodiversity provides ecosystem services (e.g., pollination, water filtration, nutrient cycling) and increases ecosystem stability/resilience to disturbance
- Greenhouse effect: greenhouse gases (CO₂, methane, water vapor) trap infrared radiation reflected from Earth's surface, warming the atmosphere — necessary for life, but human-caused excess is driving climate change
- Ocean acidification: increased atmospheric CO₂ dissolves into oceans, forming carbonic acid, lowering pH, and threatening calcifying organisms (coral, shellfish)
- Habitat fragmentation and loss reduce biodiversity by isolating populations, reducing gene flow, and shrinking available resources — currently the leading cause of species extinction
Exponential growth: dN/dt = rN
10% rule: ~10% of energy transfers to the next trophic level
Practice Question Bank — 201 questions
Unit 1: Chemistry of Life (26)
Water's high specific heat is primarily due to:
- Strong ionic bonds between neighboring molecules
- Extensive hydrogen bonding between molecules
- Its very small molecular mass and low density
- Nonpolar covalent bonds within each molecule
Hydrogen bonds must absorb significant energy to break before water's temperature rises, giving water its high specific heat.
Ice floats on liquid water because:
- Ice molecules pack more tightly than liquid water, but trapped air bubbles lift it
- Hydrogen bonds in ice form a rigid, spaced-out lattice that is less dense
- Ice has a higher proportion of oxygen atoms, which are lighter than hydrogen
- Covalent bonds in ice are longer and break apart, spacing out the molecules
The hexagonal hydrogen-bonded lattice in ice spaces molecules farther apart than in liquid water, making ice less dense.
Which best describes dehydration synthesis?
- Breaking a polymer using water
- Joining monomers and releasing water
- Denaturing a protein
- Adding water to break a peptide bond
Dehydration synthesis joins monomers into polymers, releasing one water molecule per bond formed.
A carboxyl group (-COOH) found in amino acids and fatty acids is best described as:
- Basic and able to accept a proton
- Acidic and able to donate a proton
- Nonpolar and hydrophobic
- Uncharged at all pH levels
The carboxyl group is acidic — it can ionize to -COO⁻, releasing an H⁺.
Which level of protein structure is described as the linear sequence of amino acids?
- Primary
- Secondary
- Tertiary
- Quaternary
Primary structure is simply the order of amino acids linked by peptide bonds.
A protein loses its function after being placed in boiling water. This is best explained by:
- Denaturation disrupting secondary/tertiary bonds while primary structure remains
- Hydrolysis of peptide bonds in the primary structure, breaking the chain into fragments
- Complete breakdown of the polypeptide into its individual amino acid monomers
- Conversion of the protein into a nucleic acid-like macromolecule with a new sequence
Heat denatures a protein by disrupting hydrogen bonds and other weak interactions, not the covalent peptide bonds of primary structure.
Enzymes speed up reactions by:
- Raising the free energy change (ΔG) so the products are more stable than reactants
- Converting nonspontaneous reactions into spontaneous ones by changing ΔG
- Lowering the activation energy required to reach the transition state
- Increasing the substrate concentration so the reaction reaches equilibrium faster
Enzymes lower activation energy; they do not change ΔG or reaction spontaneity.
A noncompetitive inhibitor reduces enzyme activity by:
- Binding directly at the active site, competing with the substrate for the same location
- Mimicking the substrate's shape so it blocks the active site until it is outcompeted
- Raising the enzyme's optimal temperature and pushing the enzyme out of its range
- Binding a site other than the active site and changing enzyme shape
Noncompetitive (allosteric) inhibitors bind elsewhere and change the enzyme's shape so the active site functions poorly.
Increasing substrate concentration would most effectively counteract the effect of a:
- Noncompetitive inhibitor
- Competitive inhibitor
- Denaturing agent
- Allosteric activator
Competitive inhibitors compete with substrate for the same active site, so excess substrate can outcompete the inhibitor.
Which macromolecule's monomer is a nucleotide?
- Protein
- Carbohydrate
- Lipid
- Nucleic acid
Nucleic acids (DNA, RNA) are polymers of nucleotide monomers.
Cohesion in water is responsible for:
- Water's ability to dissolve ions and polar molecules as a universal solvent
- Ice floating on liquid water as the hydrogen-bonded lattice becomes less dense
- Resistance to temperature change as heat is absorbed by hydrogen bonds
- Surface tension and movement of water up plant xylem
Cohesion (water-water attraction via H-bonds) creates surface tension and allows continuous water columns in xylem.
An enzyme functions best within a specific pH range because:
- Extreme pH changes only the charge of the substrate, leaving the enzyme's shape unchanged
- Extreme pH can disrupt the ionic and hydrogen bonds maintaining the enzyme's shape
- Every enzyme has an optimum of exactly pH 7 because water is neutral
- Extreme pH breaks the covalent peptide bonds that form the enzyme's primary structure
pH extremes disrupt the weak bonds that hold the enzyme's tertiary structure, altering the active site's shape.
Which is an example of a phospholipid's role?
- Storing long-term energy reserves as triglycerides in adipose tissue
- Forming the plasma membrane's structural bilayer
- Catalyzing biochemical reactions as a folded enzyme with an active site
- Carrying genetic information in a sequence of nucleotide bases
Phospholipids' amphipathic structure (polar head, nonpolar tails) makes them ideal for forming membrane bilayers.
The induced fit model of enzyme action states that:
- The active site is a rigid, perfectly matched shape that fits only one substrate, like a lock and key
- The substrate bends to fit the enzyme while the enzyme's shape stays completely fixed
- The enzyme changes shape permanently after one reaction and cannot be reused
- The active site changes shape slightly as the substrate binds, improving fit
Induced fit describes a slight conformational change in the enzyme's active site upon substrate binding.
Hydrolysis reactions are used by the digestive system to:
- Break down polymers into monomers by adding water
- Build polymers from monomers by removing a water molecule at each new bond
- Release oxygen gas from food molecules so cells can use it for respiration
- Denature dietary proteins by heat so enzymes can reach the peptide bonds
Digestion breaks polymers (starch, protein) into monomers via hydrolysis, adding a water molecule at each bond broken.
Which functional group would most increase a molecule's water solubility?
- Methyl group
- Hydroxyl group
- A long hydrocarbon chain
- None of these affect solubility
The polar hydroxyl group (-OH) can hydrogen bond with water, increasing solubility; methyl groups are nonpolar and decrease it.
Which bond links two amino acids together in a polypeptide?
- Peptide bond
- Glycosidic bond
- Phosphodiester bond
- Ester bond
A peptide bond forms by dehydration synthesis between the carboxyl group of one amino acid and the amino group of the next.
A fat that is solid at room temperature most likely has fatty acid tails that are:
- Unsaturated, with many cis double bonds
- Saturated, with no double bonds
- Branched with phosphate groups
- Charged and hydrophilic
Saturated fatty acids are straight and pack tightly, so the fat is solid. Cis double bonds put kinks in the chain and keep fats liquid.
Which polysaccharide do animals use for short-term energy storage?
- Starch
- Cellulose
- Glycogen
- Chitin
Animals store glucose as glycogen, mainly in liver and muscle. Plants store starch.
A solution at pH 3 has how many times more H⁺ ions than a solution at pH 6?
- 3 times
- 30 times
- 300 times
- 1000 times
The pH scale is logarithmic. Three pH units is a factor of 10 × 10 × 10 = 1000.
Which interaction mainly holds together the alpha helix and beta pleated sheet of a protein?
- Disulfide bonds between cysteine R groups
- Peptide bonds linking adjacent amino acids
- Hydrogen bonds between backbone atoms
- Ionic bonds between charged side chains
Secondary structure comes from hydrogen bonds between the backbone N-H and C=O groups, not from the R groups.
Water moving up a tall tree against gravity depends partly on adhesion, which is the attraction between:
- Water molecules and one another through hydrogen bonds
- Water molecules and the walls of xylem vessels
- Water molecules and the nonpolar, waxy cuticle of the leaf
- Oxygen atoms in neighboring water molecules sharing electrons
Adhesion to the vessel walls works together with cohesion between water molecules to pull water upward.
Which pair correctly matches a monomer with the polymer it builds?
- Glucose and protein
- Amino acid and polysaccharide
- Nucleotide and nucleic acid
- Fatty acid and starch
Nucleotides build nucleic acids, amino acids build proteins, and monosaccharides build polysaccharides. Lipids are not true polymers.
Which statement about DNA and RNA nucleotides is correct?
- Both contain deoxyribose
- RNA is double stranded and DNA is single stranded in cells
- Both use the same five carbon sugar
- DNA contains thymine and RNA contains uracil
DNA uses deoxyribose and thymine. RNA uses ribose and uracil. RNA is usually single stranded.
Why do the hydrophobic tails of phospholipids face inward in a membrane?
- They avoid contact with the surrounding water
- They are attracted to the cytoplasm
- They form covalent bonds with proteins
- They carry a positive charge
Nonpolar tails are shielded from the watery environment on both sides, so the tails cluster in the interior.
Which feature of carbon makes it the backbone of biological molecules?
- It is always charged
- It forms four covalent bonds
- It is the most abundant element in cells
- It cannot bond to hydrogen
Carbon has four valence electrons and forms four stable covalent bonds, allowing chains, rings and branches.
Unit 2: Cell Structure & Function (26)
Which structure is found in both prokaryotic and eukaryotic cells?
- Nucleus
- Mitochondria
- Ribosomes
- Endoplasmic reticulum
Both cell types contain ribosomes (though prokaryotic 70S ribosomes are smaller than eukaryotic 80S), a plasma membrane, cytoplasm, and DNA.
The best evidence for the endosymbiotic theory is that mitochondria and chloroplasts:
- Are found only in plant cells and are much larger than the nucleus
- Contain their own circular DNA, 70S ribosomes, and double membranes
- Are surrounded by a single membrane and use 80S ribosomes like the cytoplasm
- Cannot make any ATP or proteins and depend entirely on the host cell
These features closely resemble free-living bacteria, supporting the idea that these organelles originated as engulfed prokaryotes.
As a cell increases in size, its surface-area-to-volume ratio:
- Increases, improving the efficiency of exchange with the environment
- Stays constant, since surface area and volume grow at the same rate
- Decreases, limiting efficient exchange with the environment
- Becomes irrelevant, because larger cells use organelles for all exchange
Volume increases faster (cubed) than surface area (squared) as size increases, so SA:V ratio decreases, limiting exchange.
In the fluid mosaic model, membrane fluidity increases with:
- More saturated fatty acid tails (straight chains packing tightly together)
- More unsaturated fatty acid tails (kinks preventing tight packing)
- More cholesterol at low temperatures, since it always makes membranes looser
- Longer, thicker hydrophilic phospholipid heads that prevent tight packing
Unsaturated fatty acids have kinks from double bonds that prevent tight packing, increasing membrane fluidity.
Facilitated diffusion differs from active transport because facilitated diffusion:
- Requires no ATP and moves down the concentration gradient
- Requires ATP and moves solutes against their concentration gradient
- Works only for small nonpolar molecules that pass through the bilayer
- Always depends on the sodium-potassium pump to move solutes
Facilitated diffusion is passive (no ATP) and moves solutes down their gradient via channel/carrier proteins.
A red blood cell placed in a hypertonic solution will:
- Swell and burst (lyse) as water enters the cell
- Remain the same size because water movement stays balanced
- Begin dividing by mitosis as solutes increase outside the cell
- Shrivel (crenate) as water leaves the cell
In a hypertonic solution, water moves out of the cell (toward higher solute concentration), causing the cell to shrink/crenate.
A plant cell placed in a hypotonic solution becomes:
- Turgid, due to the rigid cell wall resisting excess water entry
- Plasmolyzed, as water leaves and the membrane pulls away from the wall
- Crenated, shriveling as water moves out of the cell
- Completely lysed, bursting because the wall cannot resist the water entering
Water enters the cell, but the cell wall prevents lysis, resulting in a firm, turgid cell — this is the healthy state for plant cells.
The Golgi apparatus functions primarily to:
- Modify, sort, and package proteins and lipids from the ER
- Synthesize ATP through cellular respiration using an electron transport chain
- Store the cell's genetic material and control gene transcription
- Break down worn-out organelles and foreign particles with hydrolytic enzymes
The Golgi receives products from the ER at its cis face and modifies/sorts/packages them, shipping them from its trans face.
The sodium-potassium pump is an example of:
- Simple diffusion
- Facilitated diffusion
- Active transport
- Osmosis
It moves Na⁺ and K⁺ against their gradients using ATP, making it active transport.
Which is true of both mitochondria and chloroplasts?
- Both are found only in animal cells and have a single membrane
- Both have double membranes and their own DNA
- Both perform photosynthesis and produce sugar from sunlight
- Both lack ribosomes and import all their proteins from the cytoplasm
Both organelles have double membranes and circular DNA, consistent with endosymbiotic origin.
Integral membrane proteins differ from peripheral membrane proteins in that integral proteins:
- Are only found on the membrane's outer surface
- Span or embed within the lipid bilayer
- Cannot function as receptors
- Are made of carbohydrates
Integral proteins are embedded in or span the bilayer; peripheral proteins are attached to the membrane surface only.
Which of the following would most likely increase the rate of facilitated diffusion?
- Decreasing the number of transport proteins available in the membrane
- Increasing the concentration gradient of the solute
- Adding ATP to the system to power the transport proteins
- Cooling the membrane to near freezing so the proteins move more slowly
A steeper concentration gradient increases the rate of passive transport processes like facilitated diffusion, up to a saturation point.
Lysosomes primarily function to:
- Produce ATP through oxidative phosphorylation using enzymes in their inner membrane
- Digest macromolecules, worn-out organelles, and pathogens using hydrolytic enzymes
- Synthesize lipids and detoxify drugs using enzymes embedded in their membranes
- Store starch and water in plant cells to maintain turgor pressure
Lysosomes contain hydrolytic enzymes for intracellular digestion (autophagy, pathogen destruction).
Why can eukaryotic cells generally be larger than prokaryotic cells?
- Their cells lack a plasma membrane, so size is not limited by exchange
- They do not need ribosomes because organelles make their proteins
- Membrane-bound organelles increase internal surface area and compartmentalize functions
- They reproduce more slowly, which allows more time for growth
Internal membranes (organelles) provide additional surface area for reactions, helping overcome surface-area-to-volume limitations.
A cell surrounded by a solution with the same solute concentration as its cytoplasm is in a(n):
- Hypotonic solution
- Hypertonic solution
- Isotonic solution
- Osmotic solution
Isotonic solutions have equal solute concentration, so there is no net water movement.
Cholesterol embedded in the animal cell membrane functions to:
- Anchor the membrane to the cytoskeleton, giving the cell a fixed shape that stays rigid at all temperatures
- Form channels that let polar molecules and ions cross the bilayer freely without using any cellular energy
- Buffer membrane fluidity, preventing it from becoming too fluid at high temperatures or too rigid at low temperatures
- Act as receptor proteins on the outer surface, binding signal molecules and relaying the message into the cell
Cholesterol has a dual buffering role — it restrains excess fluidity at high temperatures and prevents excess rigidity at low temperatures.
Proteins that will be secreted from a cell are typically made by ribosomes attached to the:
- Smooth endoplasmic reticulum
- Nuclear pore
- Rough endoplasmic reticulum
- Lysosome
Ribosomes on the rough ER make proteins destined for secretion, membranes or lysosomes, then pass them on through the endomembrane system.
Which evidence supports the endosymbiotic origin of chloroplasts?
- They contain their own circular DNA and ribosomes similar to bacteria
- They lack any membranes and rely on the host cell's genetic material
- They are found only in animal cells and use lysosomal enzymes
- They have a single membrane and linear DNA bound to histones like the nucleus
Circular DNA, bacteria-like ribosomes and a double membrane all point to a free-living prokaryote ancestor.
A cell has a lower water potential than its surroundings. Water will move:
- Into the cell
- Out of the cell
- Equally in both directions with no net movement
- Only through the cell wall
Water moves from higher to lower water potential, so it enters the cell with the lower value.
The sodium-potassium pump moves ions in which way?
- 2 Na⁺ out and 3 K⁺ in, without ATP
- 3 Na⁺ out and 2 K⁺ in, using ATP
- 3 Na⁺ in and 2 K⁺ out, using ATP
- Both ions down their gradients by diffusion
The pump uses ATP to move 3 Na⁺ out and 2 K⁺ in against their gradients, creating an electrochemical gradient.
Which structure is found in plant cells but not in animal cells?
- Ribosomes
- Mitochondria
- Central vacuole
- Golgi apparatus
Plant cells have a large central vacuole, a cell wall and chloroplasts. Animal cells have none of these.
Why do cells that need to exchange materials quickly tend to be small?
- A small cell has fewer organelles, so less material must be moved
- A small cell has no membrane, so materials pass through freely
- A small cell has a larger surface area relative to its volume
- A small cell has a lower metabolic rate, so less exchange is needed
As a cell grows, volume increases faster than surface area, so exchange with the environment becomes less efficient.
A student places an animal cell in distilled water. What is the most likely result?
- The cell swells and may burst
- The cell shrinks
- The cell stays the same size
- The cell becomes turgid
Distilled water is hypotonic to the cell, so water enters. Animal cells have no cell wall to resist and can lyse.
Which organelle is the main site of lipid synthesis and detoxification in many cells?
- Nucleolus
- Smooth endoplasmic reticulum
- Peroxisome only
- Rough endoplasmic reticulum
Smooth ER lacks ribosomes and synthesizes lipids and steroids and detoxifies drugs and poisons.
Which transport process moves a large particle into a cell by wrapping it in a piece of membrane?
- Osmosis
- Facilitated diffusion
- Endocytosis
- Simple diffusion
Endocytosis brings in large materials by engulfing them in a vesicle. It requires energy.
Compartmentalization in eukaryotic cells is an advantage because it:
- Eliminates the need for enzymes, because organelles carry out reactions on their own
- Allows incompatible reactions to occur at the same time in separate locations
- Prevents any exchange between organelles so that each one works in isolation
- Makes eukaryotic cells smaller than prokaryotic cells by saving space
Membrane-bound organelles keep conditions and enzymes for different reactions apart, increasing efficiency.
Unit 3: Cellular Energetics (25)
Which process directly produces the most ATP per glucose molecule?
- Glycolysis, which breaks glucose into pyruvate in the cytoplasm
- Pyruvate oxidation, which converts pyruvate into acetyl CoA
- The Krebs cycle, which completes the oxidation of acetyl CoA in the matrix
- Oxidative phosphorylation (chemiosmosis via the ETC)
Oxidative phosphorylation via the electron transport chain and chemiosmosis produces roughly 26-28 of the ~30-32 total ATP per glucose.
The main purpose of fermentation is to:
- Produce large amounts of ATP directly through substrate-level phosphorylation
- Regenerate NAD⁺ so glycolysis can continue without oxygen
- Split water to release oxygen and supply electrons to the transport chain
- Fix carbon dioxide into sugar using ATP and NADPH from earlier reactions
Fermentation regenerates NAD⁺ from NADH, allowing glycolysis to continue producing its small net ATP yield in the absence of O₂.
In the electron transport chain, the final electron acceptor in aerobic respiration is:
- NAD⁺
- Pyruvate
- Oxygen
- Carbon dioxide
Oxygen accepts electrons at the end of the ETC, combining with H⁺ to form water.
The oxygen released during photosynthesis comes from:
- Water, split during the light reactions
- Carbon dioxide, which is split during the Calvin cycle
- Glucose, which is broken down in the light reactions
- The Calvin cycle, as RuBP is regenerated and releases O₂
Photolysis of water in Photosystem II releases O₂ as a byproduct; CO₂ becomes part of the sugar produced, not O₂.
Which molecules directly power the Calvin cycle?
- ATP and NADPH from the light reactions
- Glucose and oxygen from the mitochondria
- CO₂ and H₂O, which supply the energy for fixation
- FADH₂ and pyruvate from glycolysis and the Krebs cycle
The Calvin cycle uses ATP and NADPH (produced in the light reactions) to fix CO₂ into G3P/glucose.
Chemiosmosis refers to:
- ATP synthesis driven by direct transfer of phosphate from glucose breakdown
- Diffusion of chemicals across a membrane from high to low concentration
- ATP synthesis driven by electrons flowing against a gradient to oxygen
- ATP synthesis driven by H⁺ flowing through ATP synthase down its gradient
Chemiosmosis is the process where a proton gradient drives ATP synthase to produce ATP, used in both respiration and photosynthesis.
Glycolysis occurs in the:
- Mitochondrial matrix
- Inner mitochondrial membrane
- Cytoplasm
- Chloroplast stroma
Glycolysis takes place in the cytoplasm and does not require oxygen.
An athlete experiencing muscle burn during intense exercise is most likely undergoing:
- Aerobic respiration only, with plentiful oxygen at the electron transport chain
- The Calvin cycle, which fixes carbon dioxide using ATP and NADPH
- Photosynthesis in muscle cells, which store energy as glucose
- Lactic acid fermentation due to insufficient oxygen supply
When oxygen delivery can't keep up with demand, muscle cells use lactic acid fermentation to regenerate NAD⁺.
Rubisco catalyzes which step of the Calvin cycle?
- Carbon fixation — attaching CO₂ to RuBP
- Regeneration of RuBP using ATP and G3P
- Reduction of 3-PG into G3P using ATP and NADPH
- Splitting of water to release oxygen in the light reactions
Rubisco fixes atmospheric CO₂ onto the 5-carbon RuBP, the first step of the Calvin cycle.
Which best describes the relationship between mitochondria and chloroplasts regarding ATP synthesis?
- Only mitochondria use chemiosmosis, while chloroplasts make ATP by substrate-level reactions
- Both use chemiosmosis, driven by a proton gradient across an internal membrane
- Only chloroplasts make ATP, since mitochondria use only glycolysis
- Neither uses a proton gradient, since ATP is made by phosphate transfer
Both organelles use ATP synthase and a proton gradient (chemiosmosis) to generate ATP, despite different electron sources.
Alcoholic fermentation, used by yeast, converts pyruvate into:
- Lactate
- Ethanol and CO₂
- Glucose
- Oxygen and water
Yeast converts pyruvate to acetaldehyde, releasing CO₂, then to ethanol, regenerating NAD⁺.
During the Krebs cycle, most of the energy extracted from acetyl-CoA is stored in the form of:
- ATP directly
- NADH and FADH₂ (electron carriers)
- Glucose
- Free oxygen
The Krebs cycle produces mostly NADH and FADH₂, which later fuel the ETC to make most of the cell's ATP; only 2 ATP form directly.
If a poison blocked Photosystem II specifically, which process would be directly impaired first?
- The Calvin cycle only, since it needs light directly to fix carbon
- Splitting of water and the initial electron excitation for the light reactions
- Cellular respiration, since the mitochondrial electron transport chain depends on it
- DNA replication, since light energy powers the replication fork
PS II absorbs light and splits water; blocking it stops electron flow to PS I and halts water-splitting (O₂ release).
The net ATP yield of glycolysis (before considering the electron transport chain) is:
- 0 ATP
- 2 ATP
- 4 ATP
- 36 ATP
Glycolysis uses 2 ATP to invest and produces 4 ATP, for a net gain of 2 ATP via substrate-level phosphorylation.
Which process produces ATP directly by substrate-level phosphorylation rather than chemiosmosis?
- Oxidative phosphorylation in the ETC
- Glycolysis and the Krebs cycle
- Photophosphorylation in chloroplasts
- Facilitated diffusion
Glycolysis and the Krebs cycle each generate a small amount of ATP directly (substrate-level phosphorylation), unlike the ETC's chemiosmotic mechanism.
Enzymes increase the rate of a reaction by:
- Lowering the activation energy
- Increasing the free energy of the reactants
- Being used up in the reaction
- Changing the overall free energy change
Enzymes lower the activation energy but do not change the overall free energy change or get consumed.
A competitive inhibitor can be overcome by:
- Lowering the temperature
- Increasing substrate concentration
- Adding more inhibitor
- Denaturing the enzyme
A competitive inhibitor binds the active site. Enough substrate outcompetes it, restoring the maximum rate.
During cellular respiration, the proton gradient across the inner mitochondrial membrane is used to:
- Split water
- Fix carbon dioxide
- Make ATP through ATP synthase
- Make pyruvate
Protons flow back through ATP synthase, driving the phosphorylation of ADP. This is chemiosmosis.
What is the role of NADH in cellular respiration?
- It stores carbon from glucose and carries it to the Calvin cycle
- It serves as the final electron acceptor and is reduced to water
- It carries high-energy electrons to the electron transport chain
- It breaks glucose down into two molecules of pyruvate in glycolysis
NADH is an electron carrier that delivers electrons from glycolysis and the Krebs cycle to the ETC.
Which products of the light reactions are used in the Calvin cycle?
- ATP and NADPH
- ATP and glucose
- NADH and oxygen
- Carbon dioxide and water
The light reactions make ATP and NADPH, which power the reduction of carbon in the Calvin cycle.
The Calvin cycle takes place in the:
- Thylakoid membrane
- Stroma
- Inner mitochondrial membrane
- Cytosol
The stroma holds the Calvin cycle enzymes. The light reactions occur in the thylakoid membranes.
Why does fermentation allow glycolysis to continue without oxygen?
- It produces large amounts of ATP
- It makes oxygen
- It regenerates NAD⁺
- It breaks down water
Fermentation oxidizes NADH back to NAD⁺, which glycolysis needs to keep running.
In feedback inhibition, the end product of a pathway:
- Activates the first substrate
- Binds the active site of the last enzyme only
- Is converted back to the substrate
- Inhibits an enzyme early in the pathway
The end product binds an enzyme, often allosterically, early in the pathway, shutting the pathway down when enough product exists.
Which statement about ATP is correct?
- It stores energy in its adenine base, which is released when the base is broken off the molecule
- It carries genetic information from the nucleus to ribosomes, where it directs protein building
- It couples exergonic reactions to endergonic reactions by transferring a phosphate group
- It is made in chloroplasts and is consumed completely in each reaction without being regenerated
Phosphorylation by ATP transfers energy to drive endergonic reactions. Cells constantly recycle ATP and ADP.
If the pH of the environment changes dramatically, an enzyme's activity will drop because:
- Substrate molecules disappear
- The shape of the active site can change
- Activation energy increases for all reactions
- The enzyme is used up
Changes in pH alter ionic and hydrogen bonds, changing the shape of the active site.
Unit 4: Cell Communication & Cell Cycle (25)
In cell signaling, 'transduction' refers to:
- The initial binding of a ligand to its receptor on the cell
- The final change in cell behavior, such as gene expression or enzyme activity
- The diffusion of a ligand through the plasma membrane into the cytoplasm
- The conversion of a received signal into a cellular response through a relay pathway
Transduction is the relay/amplification stage that converts receptor activation into intracellular molecular changes.
Which cell cycle checkpoint verifies that all chromosomes are properly attached to spindle fibers?
- G1 checkpoint (cell size, nutrients and DNA damage)
- M checkpoint (spindle assembly checkpoint)
- G2 checkpoint (DNA replication completeness)
- S checkpoint (the cell's commitment to dividing)
The M/spindle assembly checkpoint ensures proper chromosome attachment before anaphase proceeds.
Cyclins differ from CDKs in that:
- CDK levels oscillate through the cell cycle while cyclin levels stay fairly constant
- Both stay constant through the cycle but differ in how fast they are degraded
- Both oscillate in sync, and neither is needed unless there is DNA damage
- Cyclin levels oscillate through the cell cycle while CDK levels stay fairly constant
Cyclin concentration rises and falls at specific points in the cycle, binding and activating the constantly-present CDKs at the right time.
A mutation that converts a proto-oncogene into an oncogene is best described as a:
- Gain-of-function mutation that overstimulates cell division
- Loss-of-function mutation that removes a brake on cell division
- Silent mutation that changes the DNA but has no effect on cell division
- Mutation that affects only mitochondrial DNA and the cell's energy supply
Proto-oncogenes normally promote division; a gain-of-function mutation makes them overactive, driving excess division.
The p53 gene is best classified as a:
- Proto-oncogene
- Tumor suppressor gene
- Structural gene with no regulatory role
- Mitochondrial gene
p53 halts the cell cycle for repair or triggers apoptosis when DNA is damaged, functioning as a tumor suppressor.
Apoptosis differs from necrosis in that apoptosis is:
- Uncontrolled and damages the surrounding tissue by releasing cell contents
- Seen only in cancer cells that have lost their cell cycle controls
- A controlled, programmed process that avoids harming nearby cells
- The same process as mitosis, in which the cell divides by cytokinesis
Apoptosis is a regulated form of cell death that safely removes cells without releasing harmful contents, unlike necrosis.
During which phase of the cell cycle does DNA replication occur?
- G1
- S
- G2
- M
S phase (synthesis phase) is when DNA replication occurs, producing sister chromatids.
A cell that permanently exits the cell cycle (e.g., a mature neuron) enters:
- G0
- Prophase
- Metaphase
- Telophase
G0 is a non-dividing state that some differentiated cells enter permanently.
Second messengers like cAMP function in signal transduction primarily to:
- Directly carry the original ligand across the plasma membrane into the cytoplasm
- Amplify the signal so one receptor activation triggers a large response
- Replace the receptor so that the ligand no longer has to bind a protein
- Bind directly to DNA and alter transcription without any relay proteins
Second messengers amplify a small initial signal into a much larger intracellular response.
Sister chromatids separate during which stage of mitosis?
- Prophase
- Metaphase
- Anaphase
- Telophase
Anaphase is when sister chromatids are pulled apart to opposite poles of the cell.
Loss of contact inhibition and anchorage dependence in a cell most directly suggests:
- Normal, healthy tissue undergoing regeneration after an injury
- A cancerous cell capable of uncontrolled growth and metastasis
- A cell entering G0 and exiting the active cell cycle
- Successful apoptosis with orderly removal of a damaged cell
Cancer cells typically ignore normal growth-limiting signals like contact inhibition, allowing invasive, uncontrolled growth.
Which statement about the cell cycle checkpoints is correct?
- The G1 checkpoint verifies that spindle fibers are attached to chromosomes
- The M checkpoint verifies cell size and nutrient availability for division
- Checkpoints function only in cancer cells that divide uncontrollably
- The G2 checkpoint verifies DNA replication was completed correctly before mitosis
The G2 checkpoint ensures DNA was replicated correctly and without damage before the cell proceeds into mitosis.
A cell with damaged DNA that cannot be repaired is normally directed by p53 to:
- Continue dividing regardless of damage
- Undergo apoptosis
- Immediately enter G0 permanently with no other effect
- Convert into a stem cell
When DNA damage is irreparable, functional p53 triggers apoptosis, eliminating the potentially dangerous cell.
A phosphorylation cascade in a signal transduction pathway most directly:
- Carries the ligand directly into the nucleus and attaches it to DNA
- Relays and amplifies the signal by sequentially activating a series of proteins via kinases
- Immediately destroys the receptor so the signal cannot be repeated
- Has no influence on the final cellular response, which is set by the ligand alone
A phosphorylation cascade uses a chain of kinases, each activating the next, to relay and amplify the original signal.
Chromosomes align at the metaphase plate during which stage of mitosis?
- Prophase
- Metaphase
- Anaphase
- Telophase
During metaphase, chromosomes line up at the cell's equator (metaphase plate) before separating in anaphase.
Which sequence correctly orders the stages of cell signaling?
- Transduction, reception, response
- Response, reception, transduction
- Reception, transduction, response
- Reception, response, transduction
A ligand is received by a receptor, the message is relayed and amplified, and then the cell responds.
Why is a signal transduction pathway with several steps useful to a cell?
- It amplifies the signal and gives more points of regulation
- It slows the response so the cell avoids reacting too quickly
- It removes the need for receptors by sending the ligand through the cell
- It keeps the signal from reaching the nucleus and limits gene expression
Each step can activate many molecules, so a small signal produces a large response, and each step can be regulated.
What happens at the G1 checkpoint in a healthy cell?
- Spindle attachment to every chromosome is verified
- The cell decides whether to commit to dividing
- The cell confirms that DNA replication is complete
- Cytoplasm is divided between two daughter cells
The G1 checkpoint checks cell size, nutrients and DNA damage before committing the cell to the cycle.
During which phase do chromosomes first become visible as condensed structures?
- Interphase
- Prophase
- Telophase
- G1
Chromatin condenses into visible chromosomes in prophase, and the nuclear envelope begins to break down.
Cancer cells that divide without responding to checkpoints often have mutations that:
- Remove all of the cell's DNA so division is no longer regulated
- Increase contact inhibition and make cells stop dividing sooner
- Prevent DNA replication, which halts the cycle at the S phase
- Inactivate tumor suppressors or activate oncogenes
Loss of tumor suppressor function and gain of oncogene function both push cells toward uncontrolled division.
How does cytokinesis differ in plant and animal cells?
- Animals form a cell plate and plants form a cleavage furrow
- Plants form a cell plate and animals form a cleavage furrow
- Neither cell type undergoes cytokinesis after mitosis is complete
- Both plants and animals form a cell plate across the cell center
Animal cells pinch in with a cleavage furrow. Plant cells build a cell plate that becomes a new cell wall.
A drug blocks the formation of spindle fibers. Cells treated with it would most likely stop in:
- Metaphase
- G1
- S phase
- Cytokinesis only
Without spindle fibers, chromosomes cannot align and separate, so the cell is arrested at the spindle checkpoint in metaphase.
Quorum sensing in bacteria is an example of:
- Meiosis, in which cells divide to produce haploid gametes
- Cell signaling between cells using chemical signals
- Apoptosis, in which cells undergo programmed death
- Passive transport of solutes across the plasma membrane
Bacteria release and detect signaling molecules, and respond when the population density reaches a threshold.
Which molecule is a typical second messenger?
- DNA polymerase
- Cellulose
- cAMP
- ATP synthase
cAMP relays the message inside the cell after a signal binds a receptor at the membrane.
Which statement about apoptosis is correct?
- It always causes inflammation as cell contents spill into surrounding tissue
- It is programmed cell death used in development and to remove damaged cells
- It is the same as necrosis, which is an uncontrolled form of cell death
- It happens only in cancer cells after they stop responding to checkpoints
Apoptosis is controlled and orderly. Necrosis is uncontrolled and often triggers inflammation.
Unit 5: Heredity (25)
Crossing over occurs during which stage of meiosis?
- Prophase I
- Metaphase I
- Anaphase II
- Telophase II
Crossing over occurs during prophase I, when homologous chromosomes synapse and exchange genetic material.
For an organism with n=4 chromosome pairs, independent assortment alone can produce how many different chromosome combinations in gametes?
- 4
- 8
- 16
- 32
2ⁿ = 2⁴ = 16 possible combinations from independent assortment of 4 chromosome pairs.
A cross between a heterozygous (Rr) and a heterozygous (Rr) pea plant for a completely dominant trait produces what phenotypic ratio?
- 1:1
- 1:2:1
- 3:1
- 9:3:3:1
Rr × Rr gives genotypes 1 RR : 2 Rr : 1 rr, which is 3 dominant : 1 recessive phenotypically.
A cross between two heterozygous individuals for two independently assorting genes (AaBb × AaBb) produces which phenotypic ratio?
- 3:1
- 1:2:1
- 9:3:3:1
- 1:1:1:1
Independent dihybrid crosses produce the classic 9:3:3:1 phenotypic ratio.
Red (RR) crossed with white (WW) snapdragons produces all pink (RW) offspring. This demonstrates:
- Codominance
- Incomplete dominance
- Complete dominance
- Sex linkage
The blended pink phenotype is the hallmark of incomplete dominance, unlike codominance where both traits appear fully and separately.
AB blood type, where both A and B antigens appear on red blood cells, is an example of:
- Incomplete dominance
- Codominance
- Polygenic inheritance
- Sex linkage
Both IA and IB alleles are expressed fully and simultaneously — this is codominance, not blending.
A colorblind son is born to a mother who is a carrier (heterozygous) for the X-linked recessive trait and a father with normal vision. This is explained because the son:
- Received the trait from his father's Y chromosome, which carries the allele
- Cannot inherit X-linked traits from his mother, so a new mutation must have arisen
- Is heterozygous like his mother, so both alleles determine his phenotype
- Is hemizygous, so his single X-linked allele from his mother determines his phenotype
Males have only one X chromosome (hemizygous), so a single recessive allele inherited from the mother is enough to express an X-linked recessive trait.
Two genes located very close together on the same chromosome will:
- Tend to be inherited together, violating independent assortment, unless separated by crossing over
- Tend to assort independently of each other, following Mendel's law, unless a mutation joins them together
- Tend to be inherited separately, because the chromosome is split into pieces at the start of meiosis
- Tend to produce more recombinant offspring than nonrecombinant offspring, since nearby genes cross over often
Linked genes tend to travel together during meiosis; only crossing over can separate them, and this happens more often the farther apart the genes are.
Nondisjunction during meiosis I most directly leads to:
- Normal haploid gametes, since the chromosomes separate correctly
- Gametes with an abnormal number of chromosomes (e.g., trisomy)
- Increased crossing over, which exchanges more genetic material between homologs
- A completely new species, as a gamete carries a changed chromosome number
Failure of homologous chromosomes to separate properly produces gametes with too many or too few chromosomes.
A test cross is used to determine:
- The exact number of chromosomes in a species by counting the offspring
- Whether an organism with a dominant phenotype is homozygous or heterozygous
- Which parent contributed the Y chromosome to the offspring
- Whether a trait shows codominance rather than complete dominance
Crossing the unknown individual with a homozygous recessive reveals its genotype based on the offspring ratio produced.
Which is a source of genetic variation unique to meiosis (not mitosis)?
- Spindle formation and DNA replication
- Crossing over and independent assortment
- Point mutations and DNA replication errors
- Cytokinesis and chromosome condensation
Crossing over (prophase I) and independent assortment (metaphase I) are meiosis-specific processes generating genetic variation.
Human skin color, controlled by multiple genes with additive effects producing a continuous range of phenotypes, is an example of:
- Codominance
- Polygenic inheritance
- Sex-linked inheritance
- Incomplete dominance
Polygenic traits are influenced by multiple genes, producing a continuous distribution of phenotypes rather than discrete categories.
Meiosis II is most similar to mitosis because in both processes:
- Homologous chromosomes separate, producing two cells with half the chromosome number
- Crossing over always occurs in prophase, exchanging alleles between chromatids
- Sister chromatids separate, producing genetically identical daughter cells from each parent cell
- The chromosome number is reduced by half, giving haploid daughter cells
Both meiosis II and mitosis separate sister chromatids; meiosis I (not II) is the reductional division that separates homologs.
An offspring's blood type is O, meaning its genotype is ii. If one parent is IAi and the other is IBi, this outcome is:
- Impossible, because each parent's alleles would always give a type A or B child
- Possible — each parent could contribute the recessive i allele
- Possible only if a new mutation changed the I alleles
- Evidence that codominance failed because both I alleles should be expressed
Each heterozygous parent carries one i allele; if both contribute i, the child is ii (type O), which is fully expected under multiple allele inheritance.
Genes located far apart on the same chromosome are more likely to be separated by crossing over than genes located close together because:
- Greater physical distance increases the probability that a crossover event occurs between them
- Distance has no effect on recombination, since crossovers occur at random locations
- Close genes always cross over first, so they separate more often
- Far apart genes are on different chromosomes, so they always assort independently
Recombination frequency increases with the physical distance between two linked genes, since there is more opportunity for a crossover to occur between them.
Which event in meiosis I results in a reduction of the chromosome number?
- Homologous chromosomes separate
- Sister chromatids separate
- DNA replicates
- Crossing over occurs in anaphase
Meiosis I separates homologous pairs, cutting the chromosome number in half. Meiosis II separates sister chromatids.
The law of segregation states that:
- All traits are inherited together as a single unit from each parent
- Alleles for a trait separate into different gametes
- Dominant alleles always win and cannot be masked in the next generation
- Genes on the same chromosome assort independently into gametes
Each gamete receives only one of the two alleles for a gene.
A dihybrid cross between two heterozygotes (AaBb × AaBb) typically gives which phenotype ratio?
- 3:1
- 1:2:1
- 9:3:3:1
- 1:1:1:1
For two independently assorting genes with complete dominance, the ratio is 9:3:3:1.
A man with an X-linked recessive disorder and a carrier woman have a child. What is the chance that a son will be affected?
- 25%
- 100%
- 0%
- 50%
The mother passes either an affected X or a normal X to a son with equal probability, so half of the sons are affected.
Pink flowers appear when red and white parents are crossed. This is best explained by:
- Incomplete dominance
- Codominance
- Epistasis
- Sex linkage
In incomplete dominance the heterozygote shows an intermediate phenotype.
A chi-square test is used to determine whether:
- Two genes are on the same chromosome and are inherited together
- Observed results differ significantly from expected results
- A trait is dominant or recessive based on the offspring ratio
- A mutation has occurred in one parent's gametes
Chi-square compares observed data with expected data under the null hypothesis, using degrees of freedom to find the probability.
A pedigree shows that two unaffected parents have an affected child. The trait is most likely:
- Dominant
- Y-linked
- Recessive
- Mitochondrial
Unaffected parents can only have an affected child if both carry a hidden recessive allele.
Genes that are linked tend to:
- Assort independently because they lie far apart on the same chromosome
- Be inherited together because they are close on the same chromosome
- Be on different chromosomes and sort independently in meiosis
- Never undergo crossing over because they are physically attached
Linked genes are close together, so crossing over rarely separates them. Recombination frequency reflects the distance between them.
Down syndrome (trisomy 21) is most often caused by:
- Nondisjunction during meiosis
- A point mutation in one gene
- A viral infection
- A deletion in mitochondrial DNA
Failure of chromosome 21 to separate in meiosis produces a gamete with an extra copy.
Which gives a gamete with a unique combination of alleles that did not exist in either parent?
- Mitosis, which copies the parent cell's chromosomes exactly
- DNA replication, which makes an identical copy of each chromosome
- Binary fission, which splits a prokaryote into two identical cells
- Crossing over combined with independent assortment
Crossing over mixes alleles on homologs, and independent assortment shuffles chromosomes, producing many new combinations.
Unit 6: Gene Expression & Regulation (25)
DNA replication is described as semiconservative because:
- Both new strands are entirely newly made, and the old strands are discarded
- No original DNA is preserved, as the parent helix is degraded
- Replication copies only half the cell's DNA before the cell divides
- Each new double helix has one original strand and one newly made strand
Semiconservative replication means each daughter molecule retains one parental strand paired with one new strand.
Why is the lagging strand synthesized in short (Okazaki) fragments?
- DNA polymerase can only add nucleotides in the 3'→5' direction, opposite to the movement of the replication fork
- Helicase can unwind only short stretches of the template at a time, so the new strand must be built in pieces
- DNA polymerase can only add nucleotides in the 5'→3' direction, opposite to the replication fork's movement on that strand
- The lagging strand lacks a primer, so RNA polymerase must restart synthesis each time the fork moves forward
Since DNA polymerase synthesizes only 5'→3', the lagging strand (running away from the fork direction) must be made discontinuously.
A mutation that inserts 1 nucleotide into a gene's coding sequence would most likely:
- Swap one amino acid for another and leave the rest of the protein unchanged
- Alter only the one codon where it is inserted, leaving all later codons unaffected
- Be corrected by the ribosome during translation, giving the normal protein
- Cause a frameshift, altering every amino acid downstream of the insertion
A single nucleotide insertion (not a multiple of 3) shifts the reading frame for all codons downstream, typically producing a nonfunctional protein.
A silent mutation has no effect on the protein produced because:
- The new codon codes for a different amino acid with similar properties, so the protein folds
- The new codon still codes for the same amino acid, due to the redundancy of the genetic code
- The ribosome detects and replaces the changed codon with the original one before the amino acid is added
- The mutation changes a single base on the template but is reversed by DNA repair before transcription
The genetic code is degenerate — several codons can specify the same amino acid, so some substitutions don't change the protein.
In the lac operon, when lactose is present in the cell, it:
- Binds directly to RNA polymerase, enabling it to bind the promoter
- Binds the repressor, removing it from the operator and allowing transcription
- Binds the operator, blocking transcription of the structural genes
- Has no effect on the operon, since the repressor stays bound
Lactose acts as an inducer — it binds the repressor protein, changing its shape so it can no longer bind the operator, allowing transcription.
In gel electrophoresis, DNA fragments migrate toward the positive electrode because:
- DNA's phosphate backbone gives it a negative charge
- DNA's nitrogenous bases give it a positive charge
- Heavier DNA fragments are pulled by gravity to the bottom
- The loading dye pushes DNA toward the positive end
DNA's phosphate groups give it an overall negative charge, so it migrates toward the positive electrode in an electric field.
Which best describes the role of DNA polymerase's proofreading function?
- It detects and corrects mismatched nucleotides during replication, increasing fidelity
- It seals gaps between Okazaki fragments by joining the sugar-phosphate backbone of the new strand
- It unwinds the double helix ahead of the fork and separates the strands to prepare for replication
- It lays down short RNA primers that provide a starting point for the synthesis of new DNA strands
DNA polymerase proofreads newly added nucleotides, removing errors to keep the mutation rate very low.
During eukaryotic mRNA processing, which of the following occurs?
- Introns are added and exons are removed, producing a longer transcript
- Ribosomes bind and begin translating before transcription is complete
- A 5' cap and poly-A tail are added, and introns are spliced out
- Nothing is changed, and the mRNA is used immediately as transcribed
Eukaryotic pre-mRNA is processed by adding a 5' cap and poly-A tail and splicing out introns, leaving only exons in the mature mRNA.
DNA methylation is an example of:
- An epigenetic change that typically activates gene expression by changing the DNA base sequence itself
- A point mutation that typically silences gene expression by replacing one base with another in a gene
- A post-translational modification that typically adds sugar groups to proteins after they are made
- An epigenetic change that typically silences gene expression without altering the DNA sequence
Epigenetic modifications like DNA methylation alter gene expression heritably without changing the underlying DNA sequence.
PCR requires all of the following EXCEPT:
- Primers complementary to the target sequence
- Heat-stable DNA polymerase (Taq)
- A ribosome
- Repeated cycles of denaturation, annealing, and extension
PCR amplifies DNA using primers and heat-stable polymerase through thermal cycling — ribosomes are involved in translation, not PCR.
The trp operon is best described as:
- Inducible, normally off, and turned on when tryptophan binds the repressor
- Identical in function to the lac operon, which is inducible by its substrate
- Repressible — normally on, turned off when tryptophan acts as a co-repressor
- Found only in eukaryotes, where it controls protein synthesis
The trp operon is repressible: it's normally active, but abundant tryptophan activates the repressor to shut off transcription (negative feedback).
Heterochromatin, compared to euchromatin, is:
- Loosely packed and actively transcribed by RNA polymerase
- Found only in prokaryotes, which have no nucleus
- The site of translation, where ribosomes read mRNA
- Tightly packed and generally transcriptionally inactive
Heterochromatin is densely packed DNA that is generally inaccessible to transcription machinery, keeping those genes silent.
A restriction enzyme used in genetic engineering functions to:
- Join DNA fragments together by forming phosphodiester bonds
- Cut DNA at a specific recognition sequence, often producing sticky ends
- Synthesize new DNA strands by adding nucleotides in the 5'→3' direction
- Translate mRNA into protein by reading codons at the ribosome
Restriction enzymes recognize specific sequences and cut DNA there, generating fragments (often with complementary sticky ends) for cloning.
Which best describes the relationship between a gene's exons and introns in eukaryotic pre-mRNA processing?
- Introns are removed by splicing, and exons are joined to form mature mRNA
- Exons are removed by splicing, and introns are joined to form mature mRNA
- Both introns and exons are removed and replaced with a cap and tail
- Neither is present in pre-mRNA, which contains only regulatory sequences
Splicing removes noncoding introns, leaving only the coding exons joined together in the mature mRNA.
A missense mutation results in:
- A different amino acid being incorporated into the protein
- No change in the amino acid sequence because of the redundant code
- A premature stop codon that ends translation early
- No effect on the protein because the gene is not transcribed
A missense mutation changes the codon so that it now codes for a different amino acid than the original.
Which enzyme unwinds the DNA double helix at the replication fork?
- Ligase
- Primase
- Helicase
- RNA polymerase
Helicase breaks hydrogen bonds between the strands. Primase adds RNA primers and ligase joins fragments.
DNA polymerase can add nucleotides only to the:
- 5' end of an existing strand
- Middle of a strand
- Start of a gene without a primer
- 3' end of an existing strand
DNA polymerase synthesizes 5' to 3' by adding to a free 3' OH, so it needs a primer.
In eukaryotes, which of the following is added to pre-mRNA during processing?
- A 5' cap and a poly-A tail
- A promoter
- An operator
- A second strand
The 5' cap and poly-A tail protect the mRNA and help translation. Introns are also spliced out.
The anticodon is found on:
- mRNA
- tRNA
- DNA
- rRNA only
The anticodon on tRNA pairs with the mRNA codon in the ribosome, matching the amino acid carried.
Which mutation would most likely have the greatest effect on a protein?
- A nonsense mutation near the start of the gene
- A silent mutation that leaves the codon coding for the same amino acid
- A missense mutation at the very end of the gene, near the C-terminus
- A mutation in an intron that is removed by splicing
A nonsense mutation creates an early stop codon, producing a short, usually nonfunctional protein.
Transcription factors regulate gene expression by:
- Binding DNA and affecting whether RNA polymerase can transcribe a gene
- Cutting the DNA at specific sequences to give RNA polymerase shorter pieces
- Binding mRNA at the ribosome and controlling how fast proteins are built
- Unwinding the DNA at origins so that DNA polymerase can copy the genome
Activators and repressors bind regulatory sequences and control the rate of transcription.
In the lac operon, the repressor protein binds to the:
- Operator when lactose is absent
- Promoter when lactose is present
- Lactose permanently
- RNA polymerase only
Without lactose, the repressor sits on the operator and blocks transcription. Lactose changes the repressor so it releases.
A researcher wants to make many copies of a specific DNA segment. Which technique should be used?
- Gel electrophoresis
- PCR
- Western blot
- Karyotyping
PCR amplifies a target DNA sequence using primers and a heat-stable DNA polymerase.
Gel electrophoresis separates DNA fragments by:
- Sequence
- Color
- Size
- Gene function
Smaller fragments move farther through the gel toward the positive electrode.
Which describes the purpose of the ribosome's A, P and E sites?
- Replicating DNA
- Splicing mRNA
- Making rRNA
- Binding tRNAs during translation
The A site accepts a new tRNA, the P site holds the growing chain, and the E site releases empty tRNAs.
Unit 7: Natural Selection (25)
Homologous structures such as the forelimbs of humans, whales, and bats provide evidence for:
- Convergent evolution from unrelated ancestors facing similar pressures
- Analogous adaptation to similar environments in distant lineages
- Genetic drift as the only cause of similarity between these species
- Common ancestry, despite different current functions
Homologous structures share the same underlying anatomical origin, indicating descent from a common ancestor even though functions differ.
Bird wings and insect wings are considered analogous structures because they:
- Serve a similar function (flight) but evolved independently (convergent evolution)
- Share the same developmental origin and arose from a common ancestor's wing
- Prove that birds and insects share a recent common ancestor
- Are known only from the fossil record and show no function in living species
Analogous structures perform similar functions but arose independently, so they do NOT indicate a recent common ancestor.
If observed genotype frequencies in a population differ substantially from those predicted by Hardy-Weinberg, this suggests:
- The population is in equilibrium and no evolutionary forces are acting
- No conclusion can be drawn, since genotype frequencies are unrelated to evolution
- The population is evolving (one or more HW assumptions is being violated)
- The population size is infinite, so drift cannot alter its frequencies
Deviation from Hardy-Weinberg predictions indicates evolutionary forces (selection, drift, migration, mutation, or nonrandom mating) are acting.
A population has an allele frequency q=0.2 for a recessive allele. What is the expected frequency of homozygous recessive individuals?
- 0.2
- 0.04
- 0.4
- 0.96
q² = 0.2² = 0.04, so about 4% of the population is expected to be homozygous recessive.
A population's allele frequencies change dramatically after a natural disaster kills most of its members randomly, unrelated to genotype. This illustrates:
- Natural selection, since the survivors had better-adapted genotypes
- The bottleneck effect (a type of genetic drift)
- Gene flow, as new alleles entered from a neighboring population
- Directional selection, as one phenotype was favored over the others
The bottleneck effect is a form of genetic drift caused by a drastic, random reduction in population size.
Stabilizing selection is best illustrated by:
- Human birth weight favoring an intermediate value over extremes
- Peppered moth coloration shifting toward darker forms during industrialization
- Finch beak size splitting into two distinct extremes
- Antibiotic resistance in bacteria increasing over time
Stabilizing selection favors intermediate phenotypes and reduces variation — average birth weight has the highest survival rate.
Disruptive selection tends to:
- Increase phenotypic variation by favoring both extremes over the intermediate
- Reduce phenotypic variation by favoring the average phenotype
- Have no effect on allele frequencies, because it acts only on phenotype
- Occur only in asexual organisms, where there is no recombination
Disruptive selection favors both phenotypic extremes, which can increase variation and sometimes drive speciation.
Two populations of the same species become separated by a newly formed mountain range and evolve independently until they can no longer interbreed. This is an example of:
- Sympatric speciation
- Allopatric speciation
- Genetic drift only
- Convergent evolution
Geographic separation preventing gene flow, leading to independent divergence, defines allopatric speciation.
A mule (offspring of a horse and donkey) being sterile is an example of which reproductive isolating mechanism?
- Prezygotic — behavioral isolation
- Prezygotic — habitat isolation
- Postzygotic — hybrid sterility
- Postzygotic — hybrid inviability
Hybrid sterility is a postzygotic barrier — the hybrid survives but cannot produce viable offspring.
On a phylogenetic tree, a node represents:
- The end of a branch where a living species is placed on the tree
- The most recent common ancestor of the lineages branching from that point
- The amount of genetic change that has occurred along one lineage over time
- A complete group consisting of one ancestor and all of its descendants
Each node/branch point on a cladogram represents the most recent common ancestor shared by the descendant lineages.
Which condition is NOT required for a population to remain in Hardy-Weinberg equilibrium?
- No mutation changing the alleles
- Random mating within the population
- Natural selection actively occurring
- No gene flow into or out of the population
Hardy-Weinberg equilibrium requires the ABSENCE of natural selection (along with no mutation, no gene flow, large population, and random mating).
The high similarity of cytochrome c protein sequences between humans and chimpanzees compared to humans and yeast provides evidence that:
- Cytochrome c has no evolutionary significance because it is found in all organisms
- Humans and chimps share a more recent common ancestor than humans and yeast
- All organisms are genetically identical at the cytochrome c gene
- Molecular data cannot be used to study relationships among organisms
Greater molecular similarity generally indicates a more recent shared common ancestor.
The human appendix, a reduced structure with little current function, is best classified as a:
- Homologous structure
- Analogous structure
- Vestigial structure
- Convergent structure
Vestigial structures are reduced remnants of structures that were functional in an ancestral species.
A new plant species arises instantly from a doubling of chromosome number (polyploidy) in a single generation, without any geographic separation. This is an example of:
- Allopatric speciation
- Sympatric speciation
- Genetic drift only
- Gene flow
Sympatric speciation occurs without geographic isolation; polyploidy is a common mechanism, especially in plants.
Sexual selection, a special case of natural selection based on mating success, can explain the evolution of traits like a peacock's tail because:
- Such traits always improve survival against predators and food shortage
- Such traits arise only through genetic drift and have no effect on mating
- Such traits can increase mating success even if they carry a survival cost
- Such traits prevent gene flow and keep the population from changing
Sexual selection favors traits that increase mating success, which can evolve even when they carry some survival cost (e.g., increased predation risk).
Which statement best describes natural selection?
- Individuals change their traits during life to fit the environment, then pass them on
- Organisms always evolve toward perfect adaptation to their environment
- Individuals with heritable traits that improve survival and reproduction leave more offspring
- All traits are caused by mutations that arise within an individual's lifetime
Natural selection acts on existing heritable variation. Fitness is measured by reproductive success.
In a Hardy-Weinberg population, q² = 0.04. What is the frequency of heterozygotes?
- 0.04
- 0.32
- 0.16
- 0.64
q = 0.2 and p = 0.8, so 2pq = 2 × 0.8 × 0.2 = 0.32.
A small group of individuals starts a new population on an island. This is an example of:
- Gene flow
- Natural selection only
- The founder effect
- Directional selection
The founder effect is a type of genetic drift where the new population has a limited, unrepresentative gene pool.
Antibiotic resistance spreading in bacteria is best explained by:
- Natural selection acting on existing variation
- Bacteria deliberately choosing to adapt when exposed to the drug
- Antibiotics causing the resistance mutations in the bacteria
- Genetic drift acting as the only cause of the change
Resistant bacteria survive treatment and reproduce, so the resistance allele increases in frequency.
Which is an example of postzygotic reproductive isolation?
- Hybrid offspring that are sterile
- Mating at different times of year
- Different courtship songs
- Different habitats
Postzygotic barriers act after fertilization, such as hybrid inviability or sterility. The other choices are prezygotic.
Convergent evolution produces:
- Homologous structures in close relatives sharing a common ancestor
- Identical genomes in species that live in similar environments
- Analogous structures in unrelated species facing similar pressures
- Vestigial organs that have lost their original function
Similar selection pressures lead to similar adaptations in different lineages, such as the wings of bats and insects.
Which would increase gene flow between two populations?
- Building a barrier between the two populations
- Migration of individuals who breed in the new population
- A volcanic eruption that separates the populations
- Stronger sexual selection within each population
Gene flow is the movement of alleles between populations through migration and reproduction.
A bottleneck event usually leads to:
- Increased genetic diversity
- No change in allele frequencies
- Immediate speciation
- Reduced genetic diversity
A sharp reduction in population size removes many alleles by chance, lowering diversity.
Evidence for common ancestry includes all of the following EXCEPT:
- Shared DNA sequences among distantly related species
- Homologous structures such as limbs of different vertebrates
- Organisms always evolving toward complexity
- Transitional forms in the fossil record
Evolution has no direction toward complexity. DNA, anatomy and fossils support common descent.
On a cladogram, species that share a more recent common ancestor are:
- Always more similar in appearance
- Closer together on the tree
- Located on the same branch tip
- Older than other species
Nearness of branching points shows relatedness, not appearance.
Unit 8: Ecology (24)
Exponential population growth is best modeled by a curve that:
- Rises in a J-shape with no resource limitation
- Levels off at carrying capacity because resources become limited
- Declines steadily over time as resources are used up
- Oscillates around a fixed point as births and deaths balance
Exponential growth produces a J-shaped curve because growth rate is proportional to population size, without resource limits.
Logistic growth differs from exponential growth because logistic growth:
- Never slows down, because births always exceed deaths
- Slows as the population approaches carrying capacity due to limiting factors
- Applies only to bacteria growing in laboratory cultures
- Always produces a J-shaped curve, as growth rate is proportional to size
Logistic growth incorporates carrying capacity (K), producing an S-shaped curve as density-dependent factors slow growth.
Which is a density-dependent limiting factor?
- A hurricane destroying habitat regardless of population size
- A volcanic eruption destroying habitat in the area
- Competition for food intensifying as population density increases
- A seasonal temperature drop unrelated to population density
Density-dependent factors like competition, predation, and disease intensify as population density increases.
In a predator-prey relationship, this interaction is best classified as:
- +/+ (mutualism, in which both species benefit)
- −/− (both species are harmed by the interaction)
- +/0 (commensalism, in which one species is unaffected)
- +/− (predator benefits, prey harmed)
Predation benefits the predator (+) while harming the prey (−).
Only about 10% of energy is transferred between trophic levels mainly because:
- Producers absorb all remaining energy before it reaches the consumers
- Most energy is lost as heat through cellular respiration at each level
- Energy is destroyed at each level, which violates conservation of energy
- Consumers leave most available food uneaten, so little energy is transferred
Metabolic processes (respiration) release most energy as heat rather than passing it on to the next trophic level, following the 10% rule.
Nitrogen-fixing bacteria such as Rhizobium are important because they:
- Break down organic nitrogen compounds into N₂ gas, returning it to the atmosphere
- Live only in the ocean, where they supply nitrogen to algae
- Convert atmospheric N₂ into a usable form (ammonia/ammonium) for plants
- Compete with plants for the available nitrogen in the soil
Nitrogen-fixing bacteria convert unusable atmospheric N₂ into ammonia, which plants can use to build proteins and nucleic acids.
Which biogeochemical cycle has essentially no significant atmospheric gas phase?
- Carbon cycle
- Nitrogen cycle
- Water cycle
- Phosphorus cycle
Phosphorus cycles mainly through rock weathering, soil, and water — it lacks a major atmospheric gas component, unlike C, N, and water cycles.
Two species of birds that feed on different parts of the same tree (one on insects in the bark, one on seeds in the canopy) illustrate:
- Competitive exclusion, in which one species is eliminated from the tree
- Predation, in which one bird species feeds on the other
- Resource partitioning, reducing direct competition
- Parasitism, in which one species harms its host
Resource partitioning (niche differentiation) allows similar species to coexist by using different parts of a shared resource.
An r-selected species is most likely to:
- Produce few offspring, provide extensive parental care, and mature slowly
- Live near carrying capacity, with stable populations and long life spans
- Produce many offspring, provide little parental care, and mature quickly
- Invest heavily in each offspring, grow large, and delay reproduction
r-selected species prioritize rapid reproduction (many offspring, minimal care) suited to unstable or resource-rich environments.
Ocean acidification, caused by increased atmospheric CO₂ dissolving into seawater, primarily threatens:
- Nitrogen-fixing bacteria in the soil, which cannot tolerate acid
- Calcifying organisms such as coral and shellfish
- Freshwater fish only, since lakes are less buffered than oceans
- Terrestrial plants that rely on atmospheric CO₂ for photosynthesis
Increased CO₂ forms carbonic acid in seawater, lowering pH and interfering with calcium carbonate shell/skeleton formation.
Habitat fragmentation reduces biodiversity primarily by:
- Increasing gene flow between populations as patches are connected
- Increasing the carrying capacity of each remaining patch
- Eliminating density-dependent factors so populations grow without limit
- Isolating populations, reducing gene flow, and shrinking available resources
Fragmentation splits habitats into smaller, isolated patches, reducing gene flow and resource availability, threatening population viability.
Net primary productivity (NPP) is calculated as:
- Gross primary productivity minus the energy producers use for their own respiration
- Gross primary productivity plus the energy producers use in respiration
- Total energy stored by organisms at the top trophic level
- The rate of decomposition of dead organic matter in the ecosystem
NPP = GPP − respiration by producers; it represents the energy actually available to consumers.
Which best describes commensalism?
- One species benefits, the other is unaffected
- Both species benefit from the relationship (mutualism)
- One species benefits and the other is harmed (parasitism or predation)
- Both species are harmed by competing for the same resources
Commensalism is a (+/0) relationship — one organism benefits while the other experiences neither benefit nor harm.
A greater number of species and stronger species interactions in an ecosystem generally leads to:
- Decreased ecosystem stability and lower resilience to disturbance
- No change in ecosystem function, because species are interchangeable
- Increased ecosystem stability and resilience to disturbance
- Guaranteed extinction of keystone species due to increased competition
Higher biodiversity is generally associated with greater ecosystem stability and resilience to environmental disturbances.
The competitive exclusion principle states that:
- Two species with identical niches can coexist indefinitely in the same habitat as long as resources are abundant
- Two species that share a habitat will compete until one goes extinct, even if their niches clearly differ from each other
- Two species cannot indefinitely occupy the exact same niche in the same habitat — one will be excluded or niches will diverge
- Predators limit the number of competing species so that no single prey species can dominate the whole community over time
When two species compete for the identical niche and resources, one typically outcompetes the other, or resource partitioning allows coexistence.
A population grows exponentially until it reaches carrying capacity. After that, growth most likely:
- Continues at the same rate
- Becomes negative forever
- Levels off
- Doubles each generation
Limiting factors restrict growth near K, giving the S-shaped logistic curve.
Why are there usually fewer top predators than herbivores in an ecosystem?
- Predators are always larger, so they need more habitat
- Only about 10% of energy passes to the next trophic level
- Herbivores eat predators and so reduce their numbers
- Energy is created at each level and then lost as heat
Most energy is lost as heat and waste, so each level supports less biomass.
A keystone species is one that:
- Is the most abundant species in the community and makes up most of its biomass
- Is the top predator in a food chain and has no natural predators of its own
- Is introduced from another region and spreads rapidly, outcompeting the native species
- Has a disproportionately large effect on its ecosystem relative to its abundance
Removing a keystone species, such as a sea star in a tide pool, can reorganize the community.
Which process returns nitrogen to the atmosphere as N₂?
- Nitrogen fixation
- Denitrification
- Nitrification
- Ammonification
Denitrifying bacteria convert nitrate back to N₂ gas. Nitrogen fixation does the opposite.
Secondary succession differs from primary succession because it:
- Starts on bare rock with no soil present
- Begins with soil already present after a disturbance
- Always results in desert as the end community
- Takes longer than primary succession in the same area
After a fire or farming, soil remains, so succession proceeds faster than on new rock.
A parasite and its host represent which type of interaction?
- +/- where one benefits and the other is harmed
- +/+ where both species benefit (mutualism)
- 0/+ where one benefits and the other is unaffected (commensalism)
- -/- where both are harmed (competition)
Parasites benefit at the expense of the host.
Biomagnification occurs when:
- Energy increases at each higher level of the food chain
- Nutrients are recycled between organisms and the soil
- Producers absorb sunlight to make organic matter
- A toxin becomes more concentrated at higher trophic levels
Persistent toxins like DDT accumulate in tissues, so top predators carry the highest concentrations.
An invasive species often succeeds in a new ecosystem because it:
- Lacks natural predators or competitors there
- Always has a higher mutation rate than native species
- Is native to the area and well adapted to local conditions
- Cannot reproduce, so it does not need to compete
Without the controls of its home range, an invasive species may outcompete native species.
Which would most likely decrease biodiversity in an ecosystem?
- Protection of habitat corridors that connect populations
- Reintroduction of a keystone predator to the ecosystem
- Introduction of a dominant invasive species
- Reducing pollution entering the habitat
Invasive species can displace many natives, reducing species richness and evenness.
Hard Mode Questions — 16 questions
Unit 1: Chemistry of Life (2)
Which property of water most directly explains capillary action that helps move water up plant xylem?
- High specific heat
- Low density of ice
- Cohesion and adhesion
- Nonpolarity
Water molecules stick to each other and to xylem walls through hydrogen bonding.
The secondary structure of a protein is stabilized mainly by:
- Disulfide bridges
- Hydrogen bonds between backbone atoms
- Peptide bonds
- Hydrophobic interactions among R groups
Alpha helices and beta sheets form through backbone hydrogen bonding.
Unit 2: Cell Structure & Function (2)
Why is a high surface-area-to-volume ratio an advantage for a cell?
- It increases the cell's total volume and so allows it to hold more
- It reduces the need for a membrane around the cell
- It allows more efficient exchange of materials relative to cell volume
- It slows diffusion so that cell contents are not lost
Small cells exchange nutrients and wastes efficiently.
In facilitated diffusion, a solute moves:
- Against its concentration gradient using energy from ATP
- Packaged inside vesicles that fuse with the membrane
- Only across the nuclear envelope through nuclear pores
- Down its concentration gradient through a channel or carrier without ATP
No energy input is required because movement follows the gradient.
Unit 3: Cellular Energetics (2)
During the light reactions, electrons that replace those lost by photosystem II come from:
- Water
- Carbon dioxide
- Glucose
- NADPH
Splitting water releases electrons, protons and oxygen.
Which change would most directly decrease ATP production by oxidative phosphorylation?
- A mutation that increases the activity of ATP synthase in the inner mitochondrial membrane
- Providing the cell with more oxygen so the electron transport chain can pass electrons faster
- A higher concentration of NADH delivered to the electron transport chain from the citric acid cycle
- An uncoupler that dissipates the proton gradient across the inner mitochondrial membrane
ATP synthase relies on the proton gradient.
Unit 4: Cell Communication & Cell Cycle (2)
Cyclin-dependent kinases regulate the cell cycle by:
- Copying DNA during S phase as part of replication
- Phosphorylating target proteins when bound to a cyclin
- Forming the spindle from microtubules during mitosis
- Digesting proteins in the nucleus after they are used
Their activity rises and falls with cyclin levels.
A mutation that inactivates the p53 protein would most likely:
- Cause cells with damaged DNA to stop dividing permanently
- Allow cells with damaged DNA to keep dividing
- Trigger apoptosis in cells that have healthy, intact DNA
- Speed up DNA repair so damage is fixed before division
p53 normally halts the cycle or triggers apoptosis.
Unit 5: Heredity (2)
A heterozygous (Aa) individual is crossed with a homozygous recessive (aa). Expected phenotypic ratio of offspring:
- 3:1
- 9:3:3:1
- 1:1
- All dominant
Half the offspring are Aa and half are aa.
Two genes on the same chromosome show fewer recombinant offspring than expected under independent assortment because:
- They are located close together and tend to be inherited together
- They are located far apart and are separated by frequent crossovers
- They are on different chromosomes and assort independently of each other
- They code for proteins that are never expressed in the same cell
The closer genes are, the less often crossing over separates them.
Unit 6: Gene Expression & Regulation (2)
A nonsense mutation most likely results in:
- A single amino acid change in the protein
- A premature stop codon and a truncated protein
- A shifted reading frame for all later codons
- No change in the amino acid sequence at all
The mutation converts an amino acid codon into a stop codon.
In the lac operon, when lactose is present:
- Allolactose binds the repressor, which releases the operator, allowing transcription
- Lactose binds the operator directly, which blocks RNA polymerase from transcribing
- Allolactose activates the repressor, which tightens on the operator, stopping transcription
- The repressor is degraded by lactose, which prevents RNA polymerase from binding the promoter
The operon is inducible by lactose.
Unit 7: Natural Selection (2)
In a population at Hardy-Weinberg equilibrium, q squared = 0.16. What is the frequency of heterozygotes?
- 0.48
- 0.24
- 0.16
- 0.84
q = 0.4, p = 0.6, and 2pq = 0.48.
Which provides evidence of common ancestry?
- Homologous structures such as the limb bones of vertebrates
- Analogous structures such as the wings of bats and the wings of insects
- Similar body shapes in unrelated species living in the same habitat
- Vestigial traits that are completely absent from every related species
Similar structures with different functions reflect a shared ancestor.
Unit 8: Ecology (2)
Primary succession differs from secondary succession because primary succession:
- Begins after a forest fire
- Begins with climax species
- Occurs only in water
- Begins in an area with no soil
Pioneer species like lichens create soil first.
About how much energy is typically transferred between trophic levels?
- About 90 percent
- About 50 percent
- About 10 percent
- About 1 percent
Most energy is lost as heat and metabolic processes.
Browse all 89 flashcards as a list
Unit 1: Chemistry of Life
- Hydrogen bond
- Weak attraction between a partially positive H on one polar molecule and a partially negative atom (often O or N) on another; responsible for water's cohesion and high specific heat
- Cohesion
- Attraction between molecules of the SAME substance (water-water via H-bonds); produces surface tension and allows water columns to rise in plant xylem
- Dehydration synthesis
- Joins two monomers into a polymer, RELEASING one water molecule per bond formed
- Hydrolysis
- Breaks a polymer into monomers by ADDING a water molecule across each bond — how digestion works
- Denaturation
- Loss of a protein's 3D shape (and function) due to heat, pH change, or salt disrupting weak bonds; primary structure usually remains intact
- Active site
- Region on an enzyme where the substrate binds; shape determines the enzyme's specificity (induced fit model)
- Activation energy (Ea)
- Energy input needed to reach the transition state and start a reaction; enzymes speed reactions by lowering this, not by changing ΔG
- Competitive inhibitor
- Molecule that binds the enzyme's active site, blocking the substrate; effect can be reduced by increasing substrate concentration
- Peptide bond
- A covalent bond between the carboxyl group of one amino acid and the amino group of another, formed by dehydration synthesis.
- Saturated fat
- A lipid whose fatty acid tails have no double bonds, so the tails pack tightly and the fat is usually solid at room temperature.
- Glycogen
- A branched polysaccharide that animals use to store glucose, mainly in liver and muscle.
Unit 2: Cell Structure & Function
- Endosymbiotic theory
- Mitochondria and chloroplasts arose from free-living prokaryotes engulfed by an ancestral eukaryotic cell; supported by their own DNA, 70S ribosomes, and double membranes
- Fluid mosaic model
- Describes the plasma membrane as a dynamic phospholipid bilayer with proteins that can move laterally through it
- Facilitated diffusion
- Passive movement of polar solutes/ions through channel or carrier proteins, down their concentration gradient; no ATP required
- Active transport
- Movement of a solute AGAINST its concentration gradient, requiring ATP (e.g., the sodium-potassium pump)
- Hypotonic solution
- Lower solute concentration outside the cell than inside; water enters the cell — animal cells may lyse, plant cells become turgid
- Hypertonic solution
- Higher solute concentration outside the cell than inside; water leaves the cell — animal cells crenate, plant cells plasmolyze
- Surface area-to-volume ratio
- Decreases as a cell grows larger (volume grows faster than surface area) — limits how large a cell can get before division is favored
- Rough endoplasmic reticulum
- ER studded with ribosomes; synthesizes and folds proteins destined for secretion or membranes
- Smooth endoplasmic reticulum
- ER without ribosomes that makes lipids and steroids and detoxifies drugs.
- Water potential
- A measure of the potential energy of water, Ψ = Ψs + Ψp. Water moves from higher to lower water potential.
- Endocytosis
- A process in which a cell takes in material by engulfing it in a vesicle formed from the plasma membrane.
- Sodium-potassium pump
- A membrane protein that uses ATP to move 3 Na⁺ out and 2 K⁺ into the cell against their gradients.
Unit 3: Cellular Energetics
- Glycolysis
- Splits glucose (6C) into 2 pyruvate (3C) in the cytoplasm; produces a net 2 ATP and 2 NADH; occurs with or without oxygen
- Electron transport chain (ETC)
- Series of membrane proteins that pass electrons from NADH/FADH₂ to O₂ (final acceptor), pumping H⁺ to build the gradient used for ATP synthesis
- Chemiosmosis
- ATP synthesis driven by H⁺ flowing down its gradient through ATP synthase; used in both mitochondria (respiration) and chloroplasts (photosynthesis)
- Fermentation
- Anaerobic process that regenerates NAD⁺ from NADH so glycolysis can continue; produces lactate (animals) or ethanol + CO₂ (yeast)
- Photosystem II
- Absorbs light (P680), splits water to replace lost electrons (releasing O₂), and starts the electron transport chain to Photosystem I
- Calvin cycle
- Light-independent reactions in the stroma; uses ATP and NADPH to fix CO₂ (via rubisco) into G3P, which builds glucose
- Rubisco
- Enzyme that catalyzes carbon fixation — attaching CO₂ to RuBP in the first step of the Calvin cycle
- Substrate-level phosphorylation
- Direct transfer of a phosphate group to ADP to form ATP, occurring in glycolysis and the Krebs cycle (as opposed to chemiosmotic phosphorylation)
- Feedback inhibition
- Regulation in which the end product of a metabolic pathway inhibits an enzyme early in the pathway.
- NADH
- An electron carrier that delivers high-energy electrons from glycolysis and the Krebs cycle to the electron transport chain.
- ATP synthase
- An enzyme that uses the flow of protons down their gradient to phosphorylate ADP into ATP.
Unit 4: Cell Communication & Cell Cycle
- Signal transduction
- Process by which a cell converts an extracellular signal (ligand binding a receptor) into a specific intracellular response, often via a phosphorylation cascade
- G1 checkpoint
- Main cell cycle checkpoint (restriction point); checks cell size, nutrients, and DNA integrity before committing to division
- Cyclin-CDK complex
- Regulatory protein pair that drives the cell cycle forward — cyclin levels oscillate, CDK levels stay constant; complex phosphorylates target proteins to trigger the next phase
- Proto-oncogene
- Normal gene promoting cell division; a gain-of-function mutation converts it into an oncogene that drives uncontrolled division
- Tumor suppressor gene
- Gene (e.g., p53) that normally halts the cell cycle or triggers apoptosis when DNA is damaged; loss-of-function mutation removes this control
- Apoptosis
- Programmed, controlled cell death that removes damaged or unneeded cells without harming surrounding tissue
- Contact inhibition
- Normal cells stop dividing when they contact neighboring cells; cancer cells lose this regulatory signal and keep growing
- G2 checkpoint
- Verifies DNA replication was completed correctly and without damage before the cell is allowed to enter mitosis
- Second messenger
- A small molecule, such as cAMP, that relays and amplifies a signal inside the cell after a ligand binds a receptor.
- Cell plate
- A structure that forms during cytokinesis in plant cells and becomes the new cell wall between daughter cells.
- Quorum sensing
- Cell-to-cell signaling in bacteria that lets a population coordinate behavior when its density reaches a threshold.
Unit 5: Heredity
- Crossing over
- Exchange of genetic material between non-sister chromatids of homologous chromosomes during prophase I of meiosis; a source of genetic variation
- Independent assortment
- Random orientation of homologous chromosome pairs at the metaphase I plate, leading to 2ⁿ possible gamete combinations
- Incomplete dominance
- Heterozygote phenotype is a BLEND of both alleles (e.g., red × white → pink)
- Codominance
- Heterozygote shows BOTH parental phenotypes fully and separately (e.g., AB blood type, roan coat color)
- Sex-linked trait
- Gene located on the X chromosome; males (XY) are hemizygous, so one recessive allele is enough to express the trait
- Nondisjunction
- Failure of homologous chromosomes or sister chromatids to separate properly during meiosis, producing gametes with abnormal chromosome numbers
- Test cross
- Cross between an individual of unknown genotype (dominant phenotype) and a homozygous recessive individual, used to determine the unknown genotype
- Polygenic inheritance
- Trait controlled by multiple genes with additive effects, producing continuous variation (e.g., human height, skin color)
- Law of segregation
- The two alleles for a gene separate during gamete formation, so each gamete carries only one allele.
- Linked genes
- Genes located close together on the same chromosome that tend to be inherited together.
- Chi-square test
- A statistical test that compares observed data with expected data to see if differences are due to chance.
Unit 6: Gene Expression & Regulation
- Semiconservative replication
- Each new DNA double helix contains one original (parental) strand and one newly synthesized strand
- Leading vs lagging strand
- Leading strand synthesized continuously toward the fork; lagging strand synthesized discontinuously (Okazaki fragments) away from the fork, joined by ligase
- Frameshift mutation
- Insertion or deletion of bases NOT in a multiple of 3, shifting the reading frame for every codon downstream — usually severely disrupts the protein
- Lac operon
- Inducible prokaryotic operon; normally off, turned ON when lactose binds and removes the repressor from the operator
- PCR (polymerase chain reaction)
- Technique that exponentially amplifies a specific DNA sequence via repeated cycles of denaturation, annealing, and extension
- Gel electrophoresis
- Separates DNA fragments by size using an electric field; smaller fragments migrate farther toward the positive electrode
- Epigenetics
- Heritable changes in gene expression without a change in DNA sequence, such as DNA methylation (silences genes) and histone acetylation (activates genes)
- Restriction enzyme
- Protein that cuts DNA at a specific recognition sequence, often producing 'sticky ends' used in cloning and recombinant DNA technology
- Helicase
- An enzyme that unwinds the DNA double helix by breaking hydrogen bonds at the replication fork.
- Anticodon
- A three-nucleotide sequence on tRNA that pairs with a complementary mRNA codon during translation.
- 5' cap and poly-A tail
- Modifications added to eukaryotic pre-mRNA that protect it from degradation and help it be translated.
Unit 7: Natural Selection
- Homologous structures
- Structures with the same underlying anatomy/origin but different function across species, indicating common ancestry (e.g., human arm, whale flipper)
- Analogous structures
- Structures with similar function but different evolutionary origin, resulting from convergent evolution, NOT common ancestry (e.g., bird wing, insect wing)
- Hardy-Weinberg equilibrium
- Model describing allele/genotype frequencies in a non-evolving population; used as a null hypothesis to detect evolution
- Genetic drift
- Random change in allele frequencies due to chance, with the largest effect in small populations (bottleneck and founder effects)
- Allopatric speciation
- Formation of new species due to geographic separation preventing gene flow between populations
- Stabilizing selection
- Favors intermediate phenotypes, reduces phenotypic variation (e.g., human birth weight)
- Vestigial structure
- Reduced, functionless remnant of a structure that was functional in an ancestor (e.g., human appendix, whale pelvic bones)
- Reproductive isolation
- Prezygotic or postzygotic mechanisms that prevent gene flow between populations, allowing them to diverge into separate species
- Founder effect
- Genetic drift that occurs when a small group colonizes a new area and carries only part of the original gene pool.
- Bottleneck effect
- A sharp reduction in population size by chance that lowers genetic diversity.
- Convergent evolution
- The independent evolution of similar traits in unrelated lineages because of similar selection pressures.
Unit 8: Ecology
- Carrying capacity (K)
- Maximum population size an environment can sustainably support with available resources
- Logistic growth
- Population growth that slows as it approaches carrying capacity due to density-dependent limiting factors; produces an S-shaped curve
- 10% rule
- Only about 10% of energy is transferred from one trophic level to the next; the rest is lost mainly as metabolic heat
- Mutualism
- Symbiotic interaction in which BOTH species benefit (e.g., mycorrhizae and plant roots)
- Nitrogen fixation
- Conversion of atmospheric N₂ into ammonia/ammonium by bacteria (e.g., Rhizobium), making nitrogen usable by plants
- r-selected vs K-selected species
- r-selected: many offspring, little care, fast growth in unstable environments; K-selected: few offspring, high parental investment, thrive near carrying capacity
- Density-dependent limiting factor
- A factor whose effect on population growth intensifies as population density increases, such as competition, predation, or disease
- Trophic pyramid
- Diagram showing energy, biomass, and typically numbers decreasing at each successive trophic level, limiting food chain length
- Keystone species
- A species with an effect on community structure that is much larger than its abundance would suggest.
- Biomagnification
- The increasing concentration of a persistent toxin in organisms at higher trophic levels.
- Secondary succession
- Ecological succession that begins on soil that remains after a disturbance, such as a fire.