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Questions on prokaryotic cells and viruses
The structure of a prokaryotic cell, with its murein wall, capsule, flagellum, plasmids, circular DNA and 70S ribosomes, compared with a eukaryotic cell; binary fission; and the structure of viruses as acellular particles, with HIV as the worked example; the lytic cycle and latency, using lambda phage; and why antiviral drugs must target virus replication.
21 original questions · 64 marks · the prokaryotic cells and viruses notes · Cells, microscopy and biological organisation
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Describe the lytic cycle of lambda (λ) phage in a bacterial cell.
Mark scheme
- B1 attachment proteins on the phage bind to specific receptors on the surface of the bacterium
- B1 the phage injects its DNA into the cell, leaving the capsid outside
- B1 the viral DNA is replicated and viral proteins are made using the host's ribosomes, enzymes, nucleotides and ATP
- B1 new phage particles are assembled from the capsid proteins and copies of the DNA
- B1 a viral enzyme breaks down the cell wall so the cell bursts, or lyses, releasing the new phages
Compare the genetic material and the ribosomes of a bacterial cell with those of a eukaryotic cell.
Mark scheme
- B1 a bacterium has one circular DNA molecule, whereas a eukaryote has several linear ones
- B1 bacterial DNA is not wound round histone proteins, whereas eukaryotic DNA is
- B1 bacterial DNA lies free in the cytoplasm in the nucleoid, whereas eukaryotic DNA is enclosed by a nuclear envelope
- B1 bacterial ribosomes are 70S and smaller, whereas the ribosomes in eukaryotic cytoplasm are 80S
A student writes that a virus is simply a very small cell. Explain why this statement is wrong, referring to the structure of a virus in your answer.
Mark scheme
- B1 a virus is acellular: it has no cytoplasm and no cell-surface membrane of its own
- B1 it has no ribosomes, so it cannot make any protein for itself
- B1 it has no enzyme system for respiration, so it has no metabolism and cannot release energy from food
- B1 it consists only of DNA or RNA inside a protein capsid with attachment proteins outside, sometimes within a lipid envelope taken from a host cell
A student argues that viruses are living because they reproduce and they evolve. Evaluate this argument, referring to the structure of a virus.
Mark scheme
- B1 viruses do replicate, and their genomes do mutate and undergo natural selection, which supports the claim
- B1 replication happens only inside a host cell, using the host's ribosomes and enzymes, because a virus has no cytoplasm, no ribosomes and no metabolism of its own
- B1 outside a host cell a virus particle is metabolically inert and can even be crystallised, unlike any accepted living organism
- A1 judgement: because a virus cannot replicate or release energy independently of a host, most biologists classify it as non-living or as lying at the boundary of life, so the claim is not well supported by its structure
A culture is started with 150 bacteria, which divide by binary fission at a steady rate. Three hours later, with none of them having died, the culture contains 9600 bacteria. Calculate how many divisions have taken place, and calculate the time between one division and the next, in minutes.
Mark scheme
- M1 uses N = N₀ × 2ⁿ, so 2ⁿ = N ÷ N₀ = 9600 ÷ 150 = 64
- A1 64 = 2⁶, so n = 6 divisions
- M1 time between divisions = time elapsed ÷ number of divisions, with three hours as 180 minutes: 180 ÷ 6
- A1 30 minutes between one division and the next
Lambda phage can remain latent in a population of bacteria for many generations and then destroy the cells. Explain how.
Mark scheme
- B1 the phage DNA is inserted into the bacterial chromosome, as a prophage
- B1 a repressor protein keeps the genes of the lytic cycle switched off, so no new particles are made and the cell survives
- B1 the prophage is replicated with the chromosome at each binary fission, so every daughter cell inherits it
- B1 DNA damage, for example by ultraviolet light, removes the repressor; the prophage is cut out and enters the lytic cycle, so the cells burst
A culture is started with 200 bacteria which divide by binary fission every 30 minutes. Calculate how many bacteria are present after 5 hours, assuming that none of them die.
Mark scheme
- M1 number of divisions = 300 minutes divided by 30, giving 10 divisions
- M1 uses N = N₀ × 2ⁿ, so the calculation is 200 × 2¹⁰
- A1 an answer of 204 800 bacteria
A drug is designed to bind to the glycoprotein attachment proteins on the surface of HIV. Suggest why this drug would prevent HIV entering helper T cells, and suggest why it would have no effect on the influenza virus.
Mark scheme
- B1 the attachment proteins of HIV normally bind to the CD4 receptor found on helper T cells
- B1 with the drug bound to them the attachment proteins can no longer bind that receptor, so the virus cannot get into the cell
- B1 influenza carries different attachment proteins, which the drug is not complementary to, so it does not bind them
Explain how penicillin kills a growing bacterium, and explain why the drug is harmless to the patient's own cells.
Mark scheme
- B1 penicillin blocks the cross-linking of the murein, or peptidoglycan, cell wall
- B1 a growing bacterium therefore builds a wall it cannot hold together, so the cell bursts
- B1 human cells have no cell wall at all, so there is nothing in them for the drug to act on
Describe the stages of binary fission, in order, from a single bacterial cell to two daughter cells.
Mark scheme
- B1 the circular DNA molecule replicates, and any plasmids replicate separately and in variable numbers
- B1 the cell grows and the two DNA circles move apart to opposite ends of the cell
- B1 the cytoplasm divides and new cell wall material is laid down between the two daughter cells
Describe the structure of a bacterial flagellum, and describe how it moves the cell.
Mark scheme
- B1 a flagellum is a long protein filament, anchored in the cell membrane
- B1 it is rotated by a molecular motor embedded in the membrane
- B1 the rotation, like a propeller, drives the bacterium forward through its surroundings
Explain why plasmids, rather than mutations arising in the main chromosome, are responsible for antibiotic resistance spreading rapidly through a bacterial population.
Mark scheme
- B1 a plasmid carrying a resistance gene can be copied and passed directly from one bacterium to another, not only to daughter cells produced by division
- B1 this horizontal transfer spreads the gene through a population far faster than waiting for the same mutation to arise independently by chance in many separate cells
- B1 plasmids replicate independently of the main chromosome, so a cell can carry, and pass on, several copies at once
Bacteria have been observed since the 1670s, but a virus was not observed until the electron microscope was developed in the 1930s. Suggest why viruses were not seen so much earlier.
Mark scheme
- B1 a virus particle is typically between about 20 and 300 nm across
- B1 that is smaller than the resolving limit of a light microscope, about 200 nm
- B1 so a virus could not be distinguished from its surroundings until an instrument with a shorter wavelength, and therefore finer resolution, became available
Compare the cell wall of a bacterium with the cell wall of a plant cell, referring to the material each is built from and one consequence of the difference.
Mark scheme
- B1 a bacterial wall is built from murein (peptidoglycan), whereas a plant cell wall is built from cellulose
- B1 because the two materials are chemically different, an antibiotic such as penicillin, which blocks murein cross-linking, has no effect on a plant cell wall
- B1 both walls nonetheless resist the pressure created when water enters the cell by osmosis, stopping the cell bursting
Explain why antiviral drugs must work by inhibiting virus replication.
Mark scheme
- B1 viruses are not living cells, so they have no metabolism, ribosomes or cell wall of their own for a drug to act on
- B1 the only processes that can be blocked are the stages of replication inside the host cell, such as entry, copying of the genome, assembly or release
- B1 the drug should target a molecule coded for by the virus, such as reverse transcriptase or a viral protease, so that the host cell's own processes are not harmed
Name the substance from which a bacterial cell wall is built, and name the structure that carries genes such as antibiotic resistance and can be passed between bacteria.
Mark scheme
- A1 murein, also accepted as peptidoglycan
- A1 a plasmid, which is a small circle of DNA
Some bacteria secrete a capsule of slime outside the cell wall. State two ways in which the capsule benefits the bacterium.
Mark scheme
- B1 any one of: it retains water, it helps the cell stick to surfaces or to other bacteria, or it makes phagocytosis by a white blood cell harder
- B1 any second, different benefit from the same list
State two features that distinguish a plasmid from a bacterium's main chromosome.
Mark scheme
- B1 any one of: a plasmid is much smaller and carries far fewer genes, its genes are useful rather than essential, it replicates independently of the main chromosome, or it can be passed between bacteria
- B1 any second, different feature from the same list
Aciclovir stops herpes simplex virus copying its DNA. A patient treated with aciclovir for a cold sore recovers, but the cold sore returns months later in the same place. Suggest why.
Mark scheme
- B1 the virus remains latent in the patient's sensory neurones, where its DNA is not being copied
- B1 aciclovir acts only on replicating virus, so it cannot remove the latent DNA, which is later reactivated
In a model of phage infection, one phage infects one bacterium, and each lytic cycle releases 100 phages, every one of which infects a new bacterium. Assuming no phage is lost, calculate the number of phages released at the end of the third cycle.
Mark scheme
- M1 the number is multiplied by 100 at each cycle, so 100 × 100 × 100, or 100³
- A1 1 000 000 phages
New influenza particles stay attached to the surface of the infected cell until the viral enzyme neuraminidase cuts them free. Oseltamivir inhibits neuraminidase. Suggest how oseltamivir slows the spread of influenza in the body.
Mark scheme
- B1 new virus particles are not released from the infected cell
- B1 so fewer particles reach and infect other cells; the drug blocks the release stage of replication
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