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Flashcards · AP® Biology · Unit 2
Unit 2: Cells flashcards
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2.1 Cell Structure and Function
- What do ribosomes do, and where are they found?
- Ribosomes (rRNA and protein, no membrane) make proteins by reading mRNA and are found in all cells. Free ribosomes make proteins for the cytosol; ribosomes on rough ER make proteins for export, membranes and lysosomes.
- How do rough ER and smooth ER differ in function?
- Rough ER has bound ribosomes: protein synthesis, with new export proteins going straight into a separate compartment. Smooth ER: lipid synthesis and detoxification. Both give mechanical support and a transport route.
- What does the Golgi complex do?
- A stack of flattened sacs that checks folding, chemically modifies products (for example adding sugar chains: glycosylation) and packages them in vesicles for their destinations. It does not make proteins.
- What do lysosomes do?
- Membrane sacs of hydrolytic enzymes that digest and recycle material and help carry out apoptosis (programmed cell death). The membrane keeps digestion from harming the rest of the cell.
- How is the mitochondrion's structure linked to its function?
- A double membrane (smooth outer, folded inner called cristae) makes two compartments for aerobic respiration. Cristae add membrane area for ATP-making proteins, not more fluid.
- What is the role of the plant central vacuole?
- It stores water and nutrients and keeps turgor pressure that supports the plant. A wilting cell has a smaller vacuole because it has lost water. Animal cells have smaller, more numerous storage vacuoles.
- What path does a secreted protein take through the cell?
- Rough ER (made and labelled first) → transport vesicle → Golgi → secretory vesicle → exocytosis outside the cell. Vesicles carry proteins between ER and Golgi; proteins do not cross those membranes.
- Do plant cells have mitochondria?
- Yes. Plant cells have mitochondria as well as chloroplasts; chloroplasts (double membrane) are the site of photosynthesis.
2.2 Cell Size
- Why does surface area-to-volume ratio limit cell size?
- Everything a cell exchanges crosses its surface, but every part of its volume creates demand. As a cell grows, volume rises faster than surface area, so SA/V falls and demand per unit surface rises.
- What are the SA/V formulas for a cube and a sphere?
- Cube of side s: SA = 6s², V = s³, SA/V = 6/s. Sphere of radius r: SA = 4πr², V = (4/3)πr³, SA/V = 3/r. Cube of side 5 µm: 1.2 µm⁻¹. Use radius, not diameter, and keep the units.
- What happens to SA, V and SA/V when length is multiplied by k?
- SA is multiplied by k², V by k³, and SA/V is divided by k.
- How do cells and organisms increase surface area for exchange?
- Flat or long shapes, and membrane folds and projections that add area for almost no volume: microvilli in the gut lining, root hairs, cristae. Leaves exchange gases through stomata controlled by guard cells.
- Why does a mouse need more food per gram than a horse?
- Its higher SA/V means it loses heat faster per gram of body, so it needs a higher metabolic rate per unit mass. Smaller organisms usually have the higher rate per unit mass.
- How do you find the SA of a cylinder?
- SA = 2πrh + 2πr², and V = πr²h. A common mistake is leaving out the two ends (2πr²).
2.3 Plasma Membrane
- How are phospholipids arranged in the plasma membrane?
- In a bilayer: polar, hydrophilic phosphate heads face the watery fluid inside and outside; nonpolar, hydrophobic fatty acid tails face each other in the middle. It forms by itself as the most stable arrangement, with no energy needed.
- What is the fluid mosaic model?
- The membrane is phospholipids with proteins, steroids such as cholesterol (vertebrate animals), glycoproteins and glycolipids set into them. All can move sideways; "fluid" means components drift, not that the membrane has no shape.
- How do integral and peripheral proteins differ?
- Integral proteins pass through the bilayer (channels, carriers, receptors). Peripheral proteins sit on one face (enzymes, signalling, links to the cytoskeleton).
- How are membrane proteins positioned by their R groups?
- Hydrophobic regions (nonpolar R groups) touch the fatty acid tails. Hydrophilic regions (polar and charged R groups) face the cytosol or outside fluid, or line a pore. A whole membrane protein is not hydrophobic.
- How can you tell the outside face of a membrane in a diagram?
- Carbohydrate chains of glycoproteins and glycolipids point outward; they work in cell recognition and adhesion.
- How long must a membrane-crossing α-helix be?
- Helix length = number of amino acids × 0.15 nm. About 20 or more nonpolar amino acids are needed to cross the 3 to 4 nm hydrophobic interior; 18 give 2.7 nm.
- What does cholesterol do in animal membranes?
- It sits among the tails and keeps the membrane stable as temperature changes.
2.4 Membrane Permeability
- Why is the plasma membrane selectively permeable?
- Its interior is hydrophobic. The nonpolar tails block ions and polar molecules; an ion would have to leave its water shell to enter the tails. Charge, not size, blocks ions.
- Which molecules cross the phospholipid bilayer directly?
- Small nonpolar molecules (N₂, O₂, CO₂) cross freely. Small polar, uncharged molecules (H₂O, NH₃) cross in small amounts. Glucose and ions such as Na⁺, K⁺, Cl⁻ and H⁺ need channel or transport proteins.
- What are cell walls made of in different groups?
- Bacteria: peptidoglycan. Archaea: varied, not peptidoglycan. Fungi: chitin. Plants: cellulose. Animal cells have no wall.
- What does a cell wall do?
- It is a structural boundary, a barrier to some substances, and protection from osmotic lysis. It stops the cell expanding and bursting; the membrane, not the wall, does the fine selecting.
- How do you calculate and use standard error in membrane experiments?
- SE = s ÷ √n. Mean ± 2 SE is roughly a 95% confidence interval. Bars that do not overlap: reject H₀. Bars that overlap: fail to reject H₀. Values 10, 12, 14: s = 2, SE = 2 ÷ √3 ≈ 1.15.
- How should you word a conclusion from experimental data?
- Data support a hypothesis, or lead you to reject or fail to reject H₀. Never write "accept the null hypothesis" or "prove the hypothesis".
2.5 Membrane Transport
- What is diffusion, and what happens at equilibrium?
- Net movement from high to low concentration caused by random motion. At equal concentrations, molecules keep moving both ways but there is no net movement (dynamic equilibrium); diffusion does not stop.
- How do passive and active transport differ?
- Passive (simple diffusion, facilitated diffusion, osmosis) moves substances down their gradient with no direct metabolic energy. Active transport needs direct energy input (usually ATP) and a specific membrane protein, and can move substances from low to high concentration.
- What are endocytosis and exocytosis?
- Endocytosis folds the membrane inward to form a vesicle that takes material in (phagocytosis of bacteria). Exocytosis releases material when a vesicle fuses with the membrane (insulin release). Both need energy; cargo travels in vesicles, not through the bilayer.
- How can concentration data show active uptake?
- Find inside ÷ outside concentration. For an uncharged solute still entering, a ratio above 1 suggests active transport: 6.0 ÷ 1.5 = 4.0. Merely entering a cell is not evidence of active transport.
- Is active transport defined as movement against the gradient?
- No. It is defined by direct energy input through a membrane protein; it can go against the gradient. Facilitated diffusion uses a protein but is passive.
- Why is changing temperature a poor test of ATP dependence?
- Temperature affects diffusion and membrane fluidity as well as ATP production, so it is not a clean test. An inhibitor that only blocks ATP production is better.
2.6 Facilitated Diffusion
- What is facilitated diffusion?
- Movement of ions and large polar molecules through transport proteins, down their concentration gradient, with no energy input.
- How do channel proteins and carrier proteins differ?
- Channels form a hydrophilic pore and are fast, specific and often gated. Carriers bind a specific molecule and change shape, so they are slower. Channels do not pump ions.
- What are aquaporins?
- Channel proteins that move large quantities of water quickly (kidney collecting ducts, root cells). Water still crosses the bilayer slowly without them, and movement through them is passive.
- How do you tell simple from facilitated diffusion on a rate graph?
- Rate proportional to concentration (straight line): simple diffusion, nothing to saturate. Rate levels off at high concentration: carriers or channels saturated, so facilitated diffusion (or active transport).
- Why can ion movement polarize a membrane?
- Ions carry charge. When K⁺ leaves through K⁺ channels it carries positive charge out, and the negative ions it balanced cannot follow, so the inside becomes negative.
- What happens to facilitated diffusion if more transport proteins are added?
- The maximum rate rises; the direction is unchanged. If only the protein route doubles, do not double the whole rate, since part may come through the bilayer.
2.7 Tonicity and Osmoregulation
- What is osmosis?
- The passive net movement of water across a selectively permeable membrane. Water moves; the solutes that set up the gradient cannot cross.
- What do hypotonic, hypertonic and isotonic mean?
- They compare two solutions. A solution hypotonic to a cell has fewer solute particles, so water enters. Hypertonic: more solute, water leaves. Isotonic: no net movement. Always say what is being compared.
- What happens to animal and plant cells in different solutions?
- Animal cells lyse in hypotonic and shrivel in hypertonic solutions. Plant cells become turgid in hypotonic (the wall stops bursting), flaccid in isotonic and plasmolysed in hypertonic.
- What is the water potential equation?
- Ψ = Ψp + Ψs, in bars; water moves from higher to lower Ψ. In an open container Ψp = 0, so Ψ = Ψs.
- How do you calculate solute potential?
- Ψs = −iCRT. i = particles per unit (sucrose 1, NaCl 2, CaCl₂ 3), C in mol L⁻¹, R = 0.0831 L bar mol⁻¹ K⁻¹, T in K (°C + 273). 0.10 M sucrose at 27 °C: −(1)(0.10)(0.0831)(300) = −2.49 bar.
- How do freshwater protists osmoregulate?
- They have no wall and live in hypotonic water, so water keeps entering; a contractile vacuole pumps it out. Plant cells instead rely on the wall and central vacuole to stay turgid.
- Why plot percentage mass change in osmosis experiments?
- Starting masses differ, so raw mass change is not comparable. Percentage change = (final − initial) ÷ initial × 100; the isotonic point is where the line crosses zero.
2.8 Mechanisms of Transport
- What does active transport require?
- A membrane protein (pump) and a direct input of metabolic energy, usually ATP. Pumps are specific (binding sites fit particular ions) and saturable (maximum rate when all pumps are busy).
- How does the sodium–potassium pump work?
- 3 Na⁺ bind inside → ATP phosphorylates the pump → shape change releases Na⁺ outside → 2 K⁺ bind → phosphate released → shape returns and K⁺ is released inside. One ATP per cycle.
- Why does the Na⁺/K⁺ pump help keep the inside of the cell negative?
- Each cycle moves 3 positive charges out but only 2 in, so one net positive charge leaves. It is not a 1 : 1 exchange.
- What is an electrochemical gradient?
- A combination of a concentration difference and a charge difference across a membrane. Many resting animal cells have a membrane potential of about −70 mV (inside negative).
- Why must ion pumps keep working?
- Ions leak back through channels. If ATP runs out, pumping stops, Na⁺ leaks in and the gradient gradually runs down.
- How many ions does the Na⁺/K⁺ pump move for a given ATP use?
- 3 Na⁺ out and 2 K⁺ in per ATP. 9.0 × 10⁵ ATP per second moves 2.7 × 10⁶ Na⁺ out and 1.8 × 10⁶ K⁺ in.
2.9 Cell Compartmentalization
- What is compartmentalization, and why does it help eukaryotic cells?
- Membrane-bound organelles each hold their own enzymes, substrates and conditions, so the cell can run many reactions at once and keep opposing pathways apart.
- How do compartments minimize competing interactions?
- Opposing pathways run in different places, each space keeps its own pH (lysosome about 4.5–5, cytosol about 7.2), harmful enzymes stay contained, and enzymes and substrates are concentrated in a small volume.
- How do internal membrane folds help cells?
- Many reactions happen on membrane proteins, so folds such as cristae, stacked thylakoids and the ER network add area without adding volume. Folding adds area, not organelle size.
- How does pH relate to H⁺ concentration?
- Each 1 pH unit is a factor of 10 in H⁺; higher pH means fewer H⁺. pH 5 has 10² = 100 times more H⁺ than pH 7.
- How do you total the area of a folded membrane?
- Unfolded area plus the area added by all folds. 2.0 µm² plus 10 folds of 0.30 µm² gives 2.0 + 3.0 = 5.0 µm².
- What happens if lysosome proton pumps are blocked?
- Lysosome pH rises, the digestive enzymes slow down and undigested material builds up.
2.10 Origins of Cell Compartmentalization
- Do prokaryotes have internal organization?
- Yes, though typically no membrane-bound organelles: a nucleoid (DNA, no membrane), smaller ribosomes, a plasma membrane holding aerobic respiration proteins, and in some species thylakoids (cyanobacteria) or carboxysomes.
- What is the endosymbiotic theory?
- A host cell took in an aerobic prokaryote that became the mitochondrion. Later, a cell that already had mitochondria took in a cyanobacterium that became the chloroplast. So plants have both organelles and animals only mitochondria.
- What evidence supports endosymbiosis?
- Mitochondria and chloroplasts have two membranes, their own small circular DNA, bacteria-like ribosomes, divide by splitting like binary fission, and have DNA closest to alphaproteobacteria or cyanobacteria. The strength is in several lines agreeing.
- Why can modern mitochondria not live on their own?
- Over time most of the guests' genes moved to the nucleus or were lost, so the organelles now depend on the cell.
- How do you calculate percentage sequence identity?
- Identical positions ÷ positions compared × 100. 1,020 of 1,500 positions: 68.0%. Higher identity suggests a more recent shared ancestor.
- Why do almost all eukaryotes have mitochondria but only some have chloroplasts?
- Mitochondria were acquired first, by the common ancestor of eukaryotes; chloroplasts were acquired later, by one lineage.
Study Unit 2 further
- 2.1 Cell Structure and Function Study guide: 2.1 Cell Structure and FunctionRevision notes: 2.1 Cell Structure and FunctionPractice questions: 2.1 Cell Structure and Function
- 2.2 Cell Size Study guide: 2.2 Cell SizeRevision notes: 2.2 Cell SizePractice questions: 2.2 Cell Size
- 2.3 Plasma Membrane Study guide: 2.3 Plasma MembraneRevision notes: 2.3 Plasma MembranePractice questions: 2.3 Plasma Membrane
- 2.4 Membrane Permeability Study guide: 2.4 Membrane PermeabilityRevision notes: 2.4 Membrane PermeabilityPractice questions: 2.4 Membrane Permeability
- 2.5 Membrane Transport Study guide: 2.5 Membrane TransportRevision notes: 2.5 Membrane TransportPractice questions: 2.5 Membrane Transport
- 2.6 Facilitated Diffusion Study guide: 2.6 Facilitated DiffusionRevision notes: 2.6 Facilitated DiffusionPractice questions: 2.6 Facilitated Diffusion
- 2.7 Tonicity and Osmoregulation Study guide: 2.7 Tonicity and OsmoregulationRevision notes: 2.7 Tonicity and OsmoregulationPractice questions: 2.7 Tonicity and Osmoregulation
- 2.8 Mechanisms of Transport Study guide: 2.8 Mechanisms of TransportRevision notes: 2.8 Mechanisms of TransportPractice questions: 2.8 Mechanisms of Transport
- 2.9 Cell Compartmentalization Study guide: 2.9 Cell CompartmentalizationRevision notes: 2.9 Cell CompartmentalizationPractice questions: 2.9 Cell Compartmentalization
- 2.10 Origins of Cell Compartmentalization Study guide: 2.10 Origins of Cell CompartmentalizationRevision notes: 2.10 Origins of Cell CompartmentalizationPractice questions: 2.10 Origins of Cell Compartmentalization
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