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Cell Division – Revision Pack (B3) Multicellular: Advantages of being multicellular: • allows organism to be larger • allows for cell differentiation • allows organism to be more complex. Becoming multi-cellular requires the development of specialised organ systems, limited to: • communication between cells (nervous system) • supplying the cells with nutrients (digestive system) • controlling exchanges with the environment (respiratory and excretory system) Mitosis New cells for growth are produced by mitosis, new cells are genetically identical because they contain the same genetic information – it is a copied cell. Body cells are DIPLOID (contain two copies of each chromosome). The first step, before cells can divide is to replicate the DNA. This is done by: - ‘unzipping’ the chromosome to make it into single strands New strands forming by complementary base pairing The following steps happen in mitosis: 1) The chromosomes line up in the centre of the cell 2) They then divide; or are divided by an enzyme 3) The two copies move to two poles of the cell These cells are genetically identical. Meiosis: Cell Division – Revision Pack (B3) Gametes are produced by meiosis. Gametes are haploid (contain one chromosome from each pair). In meiosis, the chromosome number is halved and each cell is genetically different because: • One chromosome from each pair separate to opposite poles of the cell in the first division • Chromosomes divide and the copies move to opposite poles of the cell in the second division. Gametes and Fertilisation: Fertilisation results in genetic variation because: - - The two gametes (egg and sperm cells) form a diploid zygote Genes from the two chromosomes combine to determine the characteristics of that zygote The structure of a sperm cell allows it to be adapted to its function because: - PPQ(1): It has a lot of mitochondria which supplies energy It has an acrosome releases enzymes that help digest (enter) the egg membrane Cell Division – Revision Pack (B3) OCR Gateway January 2012 B1 B2 B3 PPQ(2): Cell Division – Revision Pack (B3) PPQ(3): Cell Division – Revision Pack (B3) PPQ(4): Cell Division – Revision Pack (B3) PPQ(5): Cell Division – Revision Pack (B3) PPQ(6): Mark Schemes: PPQ(1): Cell Division – Revision Pack (B3) PPQ(2): PPQ(3): PPQ(4): PPQ(5): Cell Division – Revision Pack (B3) PPQ(6): Cloning Animals: Dolly the sheep was produced by a technique called nuclear transfer. This process follows six simple steps: STEP 1: The egg cell from one sheep (sheep A) is removed STEP 2: A cell was taken from the udder of another sheep (sheep B) STEP 3: The nucleus from sheep B is put into the egg of sheep A STEP 4: This embryo is then given an electric shock to encourage it to divide STEP 5: The embryo is then implanted into a surrogate mother sheep STEP 6: The embryo then grew into a clone of sheep B This diagram is not linked to the text above; sheep A and B are different in both cases Animals could be cloned to: - Mass-produce animals with desired characteristics Provide human products through producing GM animals Produce human embryos to support stem cells for therapy Cloning Plants: Cloning plants is done by a technique called Tissue Culture; this is very easy to do and only takes three steps: STEP 1: Choose a plant with the desired characteristics Cell Division – Revision Pack (B3) STEP 2: Cut a large number of small pieces of tissue from the plant STEP 3: Grow these small pieces of tissue in test tubes or dishes containing a growth medium (NOTE – aseptic methods are used to stop the plants being infected by microbes) Advantages of cloning plants Can be sure of the characteristics of the plant since all plants will be genetically identical It is possible to mass produce plants that may be difficult to grow from seed Disadvantages of cloning plants If plants become susceptible to disease or to change in environmental conditions then all plants will be affected Lack of genetic variation Additional Notes: There are ethical issues concerning human cloning because people think that the clones will not be ‘true individual’. Cloning animals is useful in a number of ways, but it always carries risks. For example, there is suggestion that GM animals could supply replacement organisms for humans. Some people think that this could lead to disease being spread from animals to humans. Cloning animals is harder than cloning plants because animals lose their ability to differentiate early on in life, while plants retain the ability to differentiate. In other words, animals become specialised for one purpose and cannot change into different types of cells early on in their lives; it is hard to change this. Cell Division – Revision Pack (B3) Past Papers: PPQ(1): PPQ(2): Cell Division – Revision Pack (B3) PPQ(3): Cell Division – Revision Pack (B3) Mark Schemes; PPQ(1): Cell Division – Revision Pack (B3) PPQ(2): PPQ(3): Different types of cells: Plant cell Animal cell Bacterial cell Cell wall Chromosomes. presence of a nucleus NO cell wall Chromosomes. presence of a nucleus Sometimes has a cell wall single circular strand of DNA Absence of a nucleus, mitochondria and chloroplasts Measuring Growth: There are two phases of rapid growth in humans; the first is just after birth and the second is during adolescence. Cell Division – Revision Pack (B3) Girls start their second growth spurt at about 10 years old and are normally finished by 14. Boys start at about 11 and finish by the time they are 18. In both cases as the years go on the cm grown per year decreases after the initial spurt. There are different ways of measuring growth: Method Wet mass Disadvantages Hard to do for some organisms; water content of organisms can vary Dry Mass Can only be measured by driving off the water in an organism and thus killing it Length Only measures in 1 direction Differentiation: Advantages Easy to do with organisms like humans However, it does measure the true growth of the whole organism Easy to do When a cell in ‘undifferentiated’, it can develop into different cells, tissues and organs; stem cells are an example of an ‘undifferentiated’ cell. Stem cells can be obtained from embryos and could be potentially used to treat many medical conditions including Parkinson’s disease and paralysis. Many people have a problem with the use of stem cells because they think that it’s wrong that embryos are destroyed. However, some people think that this is an acceptable issue because it can be used to treat life-threatening diseases. Stem cells are also found in adults but these do not offer the same range types that embryonic cells do; also adult stem cells are not as easy to find. Plant and Animal Growth: Plant and animal growth are very different: Feature Pattern of growth Plants Often can grow continuously How growth happens Where cell division happens Mainly by cell enlargement (increase in cell size) Mainly at meristems – found at the tips of shoots and roots Animals Tend to grow to a maximum size Increasing the number of cells In most tissues Cell Division – Revision Pack (B3) Cell differentiation Past Papers: PPQ(1) Many cells can differentiate Most cells lose the ability to differentiate at an early stage Cell Division – Revision Pack (B3) PPQ(2): PPQ(3): Cell Division – Revision Pack (B3) PPQ(4): PPQ(5): Cell Division – Revision Pack (B3) Cell Division – Revision Pack (B3) PPQ(6): Cell Division – Revision Pack (B3) PPQ(7): Mark Schemes: Cell Division – Revision Pack (B3) PPQ(1): PPQ(2): PPQ(3): PPQ(4): PPQ(5): PPQ(6): Cell Division – Revision Pack (B3) PPQ(7): Cell Structure: Liver and muscle cells have large numbers of mitochondria due to large amounts of respiration taking place. Some structures in cells, such as ribosomes, are too small to be seen with the light microscope. Ribosomes are in the cytoplasm and are the site of protein synthesis. DNA Structure and Genetic Code: Describe the structure of DNA as two strands coiled to form a double helix, each strand containing chemicals called bases, of which there are four different types, with cross links between the strands formed by pairs of bases. - A chromosome is a long, coiled molecule of DNA, divided up into regions called genes. Each gene contains a different sequence of bases and codes for a particular protein. Proteins are made in the cytoplasm; a copy is made from the nucleus because the gene itself cannot leave the nucleus. The four bases of DNA are A, T, C and G. Complementary base pairings: A – T and G – C. The base pairs Cell Division – Revision Pack (B3) - Protein structure is determined by the DNA base code, to include: the base sequence determines amino acid sequence and each amino acid is coded for by a sequence of 3 bases Ribosomes are the site of protein synthesis. They are found in the cytoplasm but DNA is found in the nucleus. The genetic code needed to make a particular protein is carried from the DNA to the ribosomes by a molecule called mRNA. Making: - mRNA from DNA is called transcription Proteins from mRNA is called translation Ribosomes are smaller than mitochondria and are found in the cytoplasm. They are too small to be seen with a light microscope. The code needed to produce a protein is carried from the DNA to the ribosomes by a molecule called mRNA. DNA controls cell function by controlling the production of proteins, some of which are enzymes. Discovery of DNA Structure: Watson and Crick used data from other scientists to build a model of DNA, using Xray data showing that there were two chains wound in a helix and data indicating that the bases occurred in pairs. New discoveries, such as Watson and Crick’s, are not accepted or rewarded immediately. Here are reasons why: Cell Division – Revision Pack (B3) - Other scientists repeating or testing the work gives public confidence if their studies back up the original studies Other theories were more widely accepted PPQ(1): OCR Gateway B1 B2 B3 June 2013 PPQ(2): Cell Division – Revision Pack (B3) OCR Gateway B1 B2 B3 January 2012 PPQ(3): OCR Gateway B3 C3 P3 January 2013 PPQ(4): Cell Division – Revision Pack (B3) OCR Gateway B3 C3 P3 June 2012 PPQ(5): Cell Division – Revision Pack (B3) OCR Gateway B3 C3 P3 June 2013 Mark Schemes: PPQ(1): PPQ(2): Cell Division – Revision Pack (B3) PPQ(3): PPQ(4): PPQ(5): Cell Division – Revision Pack (B3) Selective Breeding: There are many problems with selective breeding; sometimes SB can lead to the inbreeding, where two closely related individuals mate. This can cause health problems for the species. Inbreeding can lead to a reduction in the variety of alleles in the population (this is also known as the gene pool). This can lead to: - An increased risk of harmful recessive characteristics showing up in offspring A reduction in the ability to change easily; lack of variation Genetic Engineering: Key examples of genetically engineered organisms include: - Beta-carotene being put in rice to increase vitamin A content for countries where there is little vitamin A and a reliance on rice Bacteria that have been made to contain human insulin Crop plants have been engineered so that they are frost or damage resistant There are advantages and disadvantages to genetic engineering: Advantage Organisms with the desired characteristics can be created quickly and efficiently Disadvantage There is a risk that the inserted genes may have unprecedented and harmful side effects There are also quite a lot of ethical issues surrounding genetic engineering: - Some people think it is just morally wrong Others think that there may be long-term side effects like a damage to ecosystems by GE animals / plants There are four steps to genetic engineering: Cell Division – Revision Pack (B3) STEP 1: Identify the desired characteristic STEP 2: The desired genes are identified and removed from an organism (isolation) STEP 3: These genes are then inserted into another organism STEP 4: These organisms then reproduce and replicate (This is shown on the following page in a diagram as an example) Gene therapy: The use of genetic engineering to change a person’s genes and cure certain disorders is called gene therapy. Gene therapy could involve gametes or body cells. The changing of gametes is the most controversial because it could lead to ‘designer babies’. Cell Division – Revision Pack (B3) Past Papers: PPQ(1): PPQ(2): Cell Division – Revision Pack (B3) Cell Division – Revision Pack (B3) PPQ(3): Cell Division – Revision Pack (B3) PPQ(4): Cell Division – Revision Pack (B3) PPQ(5): Cell Division – Revision Pack (B3) Mark Schemes: PPQ(1): Cell Division – Revision Pack (B3) PPQ(2): PPQ(3): Cell Division – Revision Pack (B3) PPQ(4): PPQ(5): Cell Division – Revision Pack (B3) Types of Proteins: Proteins are made of long chains of amino acids. Each protein has its own number and sequence and number of amino acids, which results in differently shaped molecules, which have different functions. The function of proteins includes: - Structural – used to build cells and tissues (limited to collagen) Hormones – carry messages to control a reaction (limited to insulin) Carrier Molecules – self explanatory (limited to haemoglobin which carries oxygen) Enzymes Enzymes: Describe enzymes as: - Biological catalysts (speed up reactions in the body) Catalysing chemical reactions occurring in living cells: respiration, photosynthesis, protein synthesis Having a high specificity for their substrate. The substrate molecule fits into the active site like a key into a lock: - This is why enzymes are described as working in a ‘lock and key mechanism’ It also explains why each enzyme can only work with a certain substrate. This is called specificity and happens because the substrate must be the right shape to fit into the active site Cell Division – Revision Pack (B3) Enzymes work best at a particular temperature and pH. This is called optimum and any change away from either optimum will slow the reaction down. When explaining how enzyme activity is affected by pH and temperature, include: - lower collision rates at low temperatures denaturing at extremes of pH and high temperatures denaturing as an irreversible change inhibiting enzyme function denaturing changing the shape of the active site It’s possible to work out how temperature affects the rate of reaction by calculating the temperature coefficient, called Q10. This is done for a 10oC change in temperature using: Q10 = rate at higher temperature Rate at lower temperature Mutations: Gene mutations may lead to the production of different proteins. Mutation may occur spontaneously but can be made to occur more often by radiation or chemicals. Mutations are often harmful but may be beneficial or have no effect. Only some of the full set of genes is used in any one cell; some genes are switched off. The genes switched on determine the functions of a cell. Changes to genes alter, or prevent the production of the protein which is normally made, this is because they change to base code of DNA, and so change the order of amino acids in the protein. PPQ(1): Cell Division – Revision Pack (B3) OCR Gateway B1 B2 B3 January 2012 PPQ(2): Cell Division – Revision Pack (B3) OCR Gateway B1 B2 B3 January 2013 PPQ(3): Cell Division – Revision Pack (B3) OCR Gateway B1 B2 B3 June 2012 PPQ(4): OCR Gateway B1 B2 B3 June 2013 PPQ(5): Cell Division – Revision Pack (B3) OCR Gateway B3 C3 P3 January 2013 PPQ(6): OCR Gateway B3 C3 P3 June 2013 PPQ(7): Cell Division – Revision Pack (B3) OCR Gateway B3 C3 P3 June 2012 Mark Schemes: PPQ(1): Cell Division – Revision Pack (B3) PPQ(2): PPQ(3): PPQ(4): Cell Division – Revision Pack (B3) PPQ(5): PPQ(6): PPQ(7): Cell Division – Revision Pack (B3) Aerobic Respiration: The symbol equation for aerobic respiration: C6H12O6 + 6O2→ 6CO2 + 6H2O Glucose + oxygen → carbon dioxide + water Measuring Respiration Rate: Two different experiments can be used to measure rate of respiration. These two ways involve: - Measuring how much oxygen is used up (the faster it’s consumed, the faster the respiration rate The rate at which carbon dioxide is made The rate of oxygen consumption can be used as an estimate of metabolic rate because aerobic respiration requires oxygen using the respiratory quotient (RQ) formula: RQ = carbon dioxide produced / oxygen used The rate of respiration is influenced by changes in temperature and pH. This is because enzymes are involved in respiration, and their activity varies with temperature and pH. Anaerobic Respiration: Muscles often don’t receive sufficient oxygen during exercise. They start to use anaerobic respiration as well as aerobic respiration. The word equation is: Glucose Lactic Acid (+ energy) Anaerobic respiration makes lactic acid which builds up in muscles. This can cause extreme pain and fatigue (tiredness). It also released much less energy per glucose molecule than aerobic respiration. Oxygen debt is when the incomplete breakdown of glucose results in the build up of lactic acid. Sometimes during recovery the heart rate and breathing rate stay high; this is because: Cell Division – Revision Pack (B3) - Rapid blood flow allows the lactic acid to be carried away to the liver Extra oxygen can be supplied, enabling the liver to break down the lactic acid ATP: ATP is a substance that is used as the energy source for many processes in cells. ATP is produced as a result of respiration. For example, one glucose molecule can release enough energy during respiration for the production of: - 38 ATP molecules by aerobic respiration - 2 ATP molecules by anaerobic respiration PPQ(1): Cell Division – Revision Pack (B3) Cell Division – Revision Pack (B3) PPQ(2): Cell Division – Revision Pack (B3) Cell Division – Revision Pack (B3) PPQ(3): Cell Division – Revision Pack (B3) PPQ(4): PPQ(5): Continued on Next Page... Cell Division – Revision Pack (B3) Cell Division – Revision Pack (B3) PPQ(6): Continued on next page... Cell Division – Revision Pack (B3) Mark Schemes: Cell Division – Revision Pack (B3) PPQ(1): PPQ(2): PPQ(3): PPQ(4): Cell Division – Revision Pack (B3) PPQ(5): PPQ(6): Blood: Red Blood Cells: Feature Reason Cell Division – Revision Pack (B3) Small size Flattened disc shape Contains haemoglobin Does not contain a nucleus Lets red blood cells pass through narrow capillaries Provides a large surface area, allowing rapid diffusion of oxygen Haemoglobin absorbs oxygen in the lungs and releases oxygen in the rest of the body Increases amount of space inside the cell for hemoglobin Plasma: Plasma transports dissolved substances around the body, including: Hormones Antibodies Nutrients, such as water, glucose, amino acids, minerals and vitamins Waste substances, such as carbon dioxide and urea Haemoglobin: Haemoglobin in red blood cells reacts with oxygen in the lungs to form oxyhaemoglobin. When this oxy-haemoglobin reaches tissues it releases the oxygen. The flattened disc shape of red blood cells (biconcave shape) provides larger surface area to volume ratio to exchange oxygen more quickly; it is the haemoglobin in red blood cells that combines with oxygen. Blood Vessels: Arteries: - transport blood away from the heart have thick muscular and elastic walls to resist the high pressure Veins: - transport blood to the heart have large lumen and valves to try and keep the blood moving back to the heart because the pressure is low Capillaries: - exchange materials with tissues; link arteries to veins have thin, permeable walls that allow substances to be transferred between the blood and the tissues The Heart: Cell Division – Revision Pack (B3) The right side: - Vena Cava (vein) brings deoxygenated blood from the body This passes through the tricuspid valve into the right ventricle The right ventricle then pumps blood up through the pulmonary artery The pulmonary artery then takes deoxygenated blood to the lungs where it gets oxygenated The left side: - The pulmonary vein brings oxygenated blood from the lungs This is passed through the bicuspid valve The left ventricle then pumps this blood up through the aorta The aorta then takes this oxygenated blood all around the body Additional Notes: The bicuspid and tricuspid are there to prevent any back-flow. This is known as a ‘double-circulatory system’. This means that the blood is at a much higher pressure and gets to the tissues at a faster rate. PPQ(1): Cell Division – Revision Pack (B3) PPQ(2): PPQ(3): Cell Division – Revision Pack (B3) Continued on next page... Cell Division – Revision Pack (B3) Cell Division – Revision Pack (B3) PPQ(4): PPQ(5): Cell Division – Revision Pack (B3) PPQ(6): Continued on next page... Cell Division – Revision Pack (B3) OCR Gateway June 2012 B3 C3 P3 PPQ(7): Mark Schemes: Cell Division – Revision Pack (B3) PPQ(1): PPQ(2): PPQ(3): Cell Division – Revision Pack (B3) PPQ(4): PPQ(5): PPQ(6): Cell Division – Revision Pack (B3) PPQ(7):