9700_w18_qp_23
A paper of Biology, 9700
Questions:
6
Year:
2018
Paper:
2
Variant:
3
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1
Aphids are small insects which feed directly on phloem sap. The salivary glands of aphids have secretory cells that make and release a variety of proteins that assist in feeding. is a transmission electron micrograph of a small area of a salivary gland cell of an aphid. mitochondrion Golgi bodies Describe the role of Golgi bodies in secretory cells, such as the salivary gland cells of aphids. Explain why secretory cells have large numbers of mitochondria. Mitochondria are partly controlled by the nucleus, but can also function independently. Suggest the features of mitochondria that allow them to function independently of the nucleus. Aphids are important vectors of plant viral diseases. Describe the structure of a typical virus. Suggest how viruses are able to pass from one plant cell to the next without crossing membranes.
1. Cell structure  →  1.2. Cells as the basic units of living organisms
12. Energy and respiration  →  12.2. Respiration
14. Homeostasis  →  14.2. Homeostasis in plants
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2
Proteins are macromolecules composed of many amino acids. Two amino acids are represented in the diagram in . Complete the diagram to show how the two amino acids react together to form a dipeptide. N H H H OH O R1 C C + N H H H OH O R2 C C State what is represented by R1 and R2 in . Amylose and cellulose are polysaccharides. shows the structure of part of a cellulose molecule. H OH CH2OH H H H O O O O H OH CH2OH H H H O H OH CH2OH H O O H OH CH2OH H O O With reference to , state how the structure of a cellulose molecule differs from the structure of an amylose molecule. Cellulose is the main component of plant cell walls. Explain why cellulose is suitable as a component of plant cell walls.
2. Biological molecules  →  2.2. Carbohydrates and lipids
2. Biological molecules  →  2.3. Proteins
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3
is a diagram of a monomer of the nucleic acid, messenger RNA. F E D Name D, E and F in . D E F State one way in which the structure of DNA differs from the structure of messenger RNA. Telomeres are repeating sequences of bases located at the ends of DNA molecules. These repeating sequences do not code for proteins. The enzyme telomerase ensures that telomeres do not shorten each time DNA is replicated. A shows the end of a DNA molecule during replication. DNA polymerase cannot attach to the region labelled X, so it cannot complete the synthesis of the new strand without the action of telomerase. Telomerase synthesises additional lengths of DNA that are added to the telomere. These additional lengths are used by DNA polymerase to complete the process of replication. B is an enlarged view of region X to show the action of the enzyme telomerase. A T 5’ 3’ 3’ 5’ A T A A T T A T A A T G C G C G C G C G C G C T A T A A T G C G C G T T A G G G T T A G X B T T A T C A A A G C G G C T C C C A U A C A U free nucleotides telomerase template RNA Telomerase contains a short length of RNA that acts as a template for the synthesis of DNA as shown in B. Explain how a molecule of telomerase synthesises additional lengths of DNA. Telomerase is not present in prokaryotic cells. Suggest why prokaryotes do not have telomerase. One of the ways to diagnose lung cancer is to determine the concentration of telomerase in cells from the lining of the bronchus. Explain why determining the activity of telomerase may be useful in the diagnosis of lung cancer.
6. Nucleic acids and protein synthesis  →  6.1. Structure of nucleic acids and replication of DNA
5. The mitotic cell cycle  →  5.1. Replication and division of nuclei and cells
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4
Describe the roles of the sinoatrial node (SAN) and the atrioventricular node (AVN) in the initiation and control of the cardiac cycle. The Purkyne fibres pass down the septum and extend to the cardiac muscle at the base of the heart. Explain why it is important that the Purkyne fibres extend to the base of the heart. The activity of the SAN is controlled by the nervous system. Noradrenaline is released by nerve cells in the SAN. shows the role of noradrenaline in causing calcium ions (Ca2+) to enter a cell in the SAN. noradrenaline phospholipid bilayer ATP cAMP (second messenger) inactive enzyme active enzyme active enzyme opens channel protein Ca2+ Ca2+ Ca2+ Ca2+ Ca2+ small gap cell surface membrane of SAN cell With reference to , outline the process of cell signalling.
8. Transport in mammals  →  8.3. The heart
14. Homeostasis  →  14.1. Homeostasis in mammals
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5
The bacteria that cause tuberculosis (TB) can be found in many parts of the body including the lungs. State the name of the bacterium that causes TB. The presence of the pathogen in the lungs attracts phagocytes to the area of infection. The phagocytes release elastase, which digests elastin. Many people with TB feel tired all the time. Suggest and explain how the effect of phagocytes on tissues in the lungs leads to people feeling tired all the time. Discuss the biological factors and social factors that make TB a difficult disease to control.
10. Infectious diseases  →  10.1. Infectious diseases
11. Immunity  →  11.1. The immune system
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6
As part of a study of the mitotic cell cycle, a student made stained sections of a root tip of onion, Allium cepa, and observed them with a light microscope. The student made drawings of six of the cells, A to F, using the high power of the microscope, as shown in . A B C D E F Complete Table 6.1 to show the sequence of stages in the mitotic cell cycle, using the letters, A to F, as shown in . Table 6.1 sequence of stages cell A Table 6.2 shows some events that occur during the mitotic cell cycle in A. cepa. Complete Table 6.2 by naming the stage of the cell cycle when each event occurs. Table 6.2 event in the cell cycle name of the stage in the cell cycle DNA replication division of centromeres condensation of chromatin contraction of spindle fibres organisation of chromosomes at the equator metaphase Explain the importance of mitosis in the immune response.
5. The mitotic cell cycle  →  5.1. Replication and division of nuclei and cells
5. The mitotic cell cycle  →  5.2. Chromosome behaviour in mitosis
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