Unit 2 · Practice for the Topic 2.5 end-of-topic test
A lab prepares two solutions, each 0.20 mol/L and each one liter: one of glycine, an amino acid whose molecules weigh 75 g per mole, and one of tryptophan, an amino acid whose molecules weigh 204 g per mole.
How do the numbers of dissolved amino acid molecules in the two liters compare?
In a kidney, fluid inside a tube holds urea at 0.30 mol/L. Blood flowing beside the tube holds urea at 0.005 mol/L. The wall between them lets urea through.
Which way is down urea's concentration gradient?
A drop of perfume evaporates on a desk in a still room with no drafts. A minute later a student at the far side of the room smells it.
Why does the scent reach the far side of the room?
In a fish's gill, water flowing past holds oxygen at 8 mg/L, and the blood inside the gill holds oxygen at 3 mg/L. Oxygen molecules cross the thin gill wall in both directions.
What is the net movement of oxygen at the gill?
A fish tank is divided by a fine mesh that dissolved salt ions can cross. Both halves have held salt at 0.5 g/L for a day. A student says: "The salt ions have stopped crossing the mesh, because the two sides are equal."
Which statement corrects the student?
Molecule V is a small nonpolar molecule. It is at 6 units per liter outside a skin cell and 1 unit per liter inside, and it enters the cell straight through the bilayer while the cell's supply of ATP is blocked.
How should this crossing be classified?
Inside a leaf cell, sucrose is at 0.30 mol/L; in the watery spaces of the cell wall outside it, sucrose is at 0.02 mol/L. Sucrose is a large polar molecule, and the cell's sucrose carriers are all shut.
What keeps the sucrose more concentrated inside the cell than outside?
A cell lining the stomach pushes hydrogen ions (H⁺) out into the stomach fluid, where H⁺ is at 150 mmol/L (thousandths of a mol/L). Inside the cell, H⁺ is at 0.0001 mmol/L.
What must this crossing involve?
A cell lining a newborn's gut takes in whole antibody proteins from milk. Each antibody is far too large for any channel or carrier. Under the microscope the cell's membrane is seen folding around a cluster of antibodies and closing behind them.
How do the antibodies get into the cell, and where are they once inside?
A cell in a mammary gland holds milk proteins inside vesicles. The vesicles move to the plasma membrane and fuse with it, and the proteins appear in the milk outside. When a drug blocks the cell's ATP production, the vesicles stay inside and protein stops appearing in the milk.
What do these observations show?
(a) Identify the direction of crossing 1 relative to fructose's concentration gradient, and state the two concentrations that tell you. (1 point)
A full-credit answer: Fructose moves down its concentration gradient, from 12 mmol/L in the gut fluid to 1 mmol/L in the cytosol: from where it is more concentrated to where it is less.
Check the box for each point your answer earns
Accept: "from high to low" with the two values quoted.
Common slip: Reading 'through a protein' as a sign of uphill movement. The direction is set by the two concentrations, and 12 to 1 mmol/L is downhill.
(b) Describe what the two observations about crossing 2 show about how amino acid L enters. (1 point)
A full-credit answer: L moves from 0.5 mmol/L in the gut fluid to 8 mmol/L in the cytosol, which is against its concentration gradient, and the uptake stops when the cell's ATP is blocked. Together these show that the cell spends energy from ATP to move L uphill through a pump: active transport.
Check the box for each point your answer earns
Accept: 'uphill' for against the gradient; both observations are needed for the point.
Common slip: Naming active transport from the protein alone. Channels and carriers are proteins too; what marks active transport is movement against the gradient paid for with ATP.
(c) Explain why crossing 1 costs the cell nothing while crossing 2 must cost it energy. (1 point)
A full-credit answer: Fructose is moving down its gradient. Particles move constantly and at random, so more leave the crowded gut fluid than return, and the net movement into the cell happens by itself; the protein only gives fructose a route through the membrane it cannot cross alone. This is facilitated diffusion, a form of passive transport, and it costs nothing. L is moving against its gradient, from 0.5 to 8 mmol/L. Random movement alone gives a net flow the other way, so the cell must spend energy, from ATP, to push L uphill.
Check the box for each point your answer earns
Accept: "downhill is free; uphill has to be paid for" with the mechanism (random movement gives a net flow downhill only) stated.
Common slip: Saying crossing 1 is free because fructose is a sugar the cell needs. What makes it free is the direction: down the gradient, which random movement supplies on its own.
(d) Identify the mechanism at crossing 3 and at crossing 4, giving the clue in the description that decides each. (1 point)
A full-credit answer: Crossing 3 is simple diffusion: oxygen moves down its gradient straight through the bilayer, with no protein, which is the route open to a small nonpolar molecule. Crossing 4 is exocytosis: mucus is far too large for any protein door, so it leaves inside a vesicle that fuses with the plasma membrane and opens outward.
Check the box for each point your answer earns
Accept: 'passive transport through the bilayer' for crossing 3. Both mechanisms with their clues are needed for the point.
Common slip: Calling crossing 4 active transport because it costs energy. Exocytosis does cost energy, but it moves a whole vesicle's worth of material, not one molecule through a pump.
(e) Predict what happens to crossing 1 if fructose builds up in the cytosol until it is also at 12 mmol/L, and justify your prediction. (1 point)
A full-credit answer: When fructose is at 12 mmol/L on both sides, the net movement into the cell stops. Fructose molecules keep crossing through the protein, but as many leave the cell as enter it, so the concentration inside stops rising: a dynamic equilibrium. The molecules still move; only the net movement is zero.
Check the box for each point your answer earns
Accept: "no net movement; equal traffic both ways". Do not award the point for "fructose stops moving" or "the protein closes".
Common slip: Saying the fructose molecules stop moving, or the carrier shuts. They keep crossing both ways; equal concentrations give equal traffic, so no net change.
(a) Describe how an ion such as Na⁺ can cross a plasma membrane, and what stops it crossing the bilayer on its own. (1 point)
A full-credit answer: An ion such as Na⁺ crosses the membrane only through a membrane protein: a channel when it moves down its gradient, or a pump when it is moved against it. It cannot cross the bilayer on its own because the hydrocarbon tails in the middle of the membrane carry no charges or partial charges, so water holds the ion and nothing in the interior can take it.
Check the box for each point your answer earns
Accept: "the oily interior has nothing to hold a charge, so ions need a protein".
Common slip: Saying Na⁺ is too big to cross. It is one of the smallest particles present; its charge, held by water, is what keeps it out of the interior.
(b) Explain what trial 2 shows about how the cells normally keep their Na⁺ at 10 mmol/L. (1 point)
A full-credit answer: In trial 2 the cells could make no ATP, and their Na⁺ climbed from 10 toward 200 mmol/L. So the low Na⁺ in trial 1 was being maintained by work: a pump spending ATP moves Na⁺ out against its gradient as fast as it enters. With no ATP the pump stops, and Na⁺ diffuses in down its gradient until the inside approaches the outside.
Check the box for each point your answer earns
Accept: "a pump using ATP removes Na⁺ as fast as it enters; stop the pump and diffusion evens the sides out".
Common slip: Saying the drug let Na⁺ in. The drug only stopped the ATP supply; Na⁺ was entering all along, and what failed was the pumping out.
(c) Propose one further trial to test whether the blocked channel of trial 3 is the route by which Na⁺ entered in trial 2, and predict its result. (1 point)
A full-credit answer: Treat cells with both the drug that blocks ATP and the compound that blocks the channel, then add labeled Na⁺ for an hour. If the channel is the route Na⁺ used in trial 2, almost no labeled Na⁺ will appear inside and the total will stay near 10 mmol/L even though the pump is off. If Na⁺ still rises toward 150 mmol/L, it is entering by some other route.
Check the box for each point your answer earns
Accept: any design that combines the two treatments (or blocks the channel in ATP-blocked cells) with a prediction that matches the claim being tested.
Common slip: Proposing to repeat trial 3 with more cells. The question is whether the channel is the entry route when the pump is off, which needs both treatments in one trial.
(d) Justify the claim that these cells keep their Na⁺ low by combining a channel and a pump, using the results of all three trials. (1 point)
A full-credit answer: Trial 3 shows the channel is the way in: with it blocked, almost no labeled Na⁺ reaches the cytosol. Trial 2 shows the pump is the way out and that it runs on ATP: with ATP blocked, the Na⁺ that leaks in through the channel is no longer removed, and the inside climbs to 150 mmol/L. Trial 1 shows the two working together: labeled Na⁺ enters through the channel, yet the total stays at 10 mmol/L because the pump, spending ATP, sends Na⁺ back out against its gradient as fast as it comes in.
Check the box for each point your answer earns
Accept: the three trials tied to entry, removal and the steady state in any order. Do not award the point for a justification that uses only one trial.
Common slip: Justifying from trial 2 alone. The claim has two parts, a channel for entry and a pump for removal, and each needs its own trial as evidence.