Revision questions - biochemistry and metabolism Flashcards

1
Q
  1. What is the metabolic pathway by which glucose is broken down in the absence of oxygen? (slide 4)
    1. Glycolysis
    2. Electron transport chain
    3. Phosphorylation
    4. TCA cycle
A

a. Glycolysis

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2
Q
  1. Each step in a metabolic pathway usually requires something to help it proceed. What is this chemical? (slide 5)
    1. Acid
    2. Hormone
    3. Enzyme
    4. Protein
A

c. Enzyme

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3
Q
  1. Enzyme names always end in what 3 letters? (slide 5)
    1. –ate
    2. –ase
    3. –ion
    4. –ene
A

b. –ase

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4
Q
  1. All the steps in glycolysis produce ATP? (slide 6)
    1. True
    2. False
A

b. False

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5
Q
  1. In cellular metabolism what is the order of breakdown to provide energy? (slide 10)
    1. Carbohydrate, protein, lipids
    2. Carbohydrate, lipids, protein
    3. Protein, lipids
    4. Carbohydrate, lipids
A

d. Carbohydrate, lipids

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6
Q
  1. The breakdown of nutrients or metabolites is called what? (slide 10)
    1. Anabolism
    2. Catabolism
    3. Metabolism
A

b. Catabolism

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7
Q
  1. Where is most ATP formed? (slide 13)
    1. The mitochondria
    2. The nucleus
    3. The ribosomes
    4. The cell cytosol
A

a. The mitochondria

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8
Q
  1. Anabolism produces energy (slide 15)
    1. True
    2. False
A

b. False

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9
Q
  1. Cells need to synthesise new organic modules. Which of the following is not a main requirement? (slide 16)
    1. Structural maintenance and repairs
    2. Growth
    3. Production of secretions
    4. Catabolism of nutrients
A

d. Catabolism of nutrients

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10
Q
  1. Metabolic turnover is: (slide 17)
    1. The one-off replacement of cell membranes
    2. The continual replacement of mitochondria
    3. The continual usage and replacement of glycogen in the liver
    4. The continual replacement of cell components
A

d. The continual replacement of cell components

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11
Q
  1. All cell components are replaced at the same rate. (slide 17)
    1. True
    2. False
A

b. False

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12
Q
  1. Metabolic turnover does not require ATP (slide 18)
    1. True
    2. False
A

b. False

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13
Q
  1. What are the two principal metabolic pathways in the mitochondria? (slide 21)
    1. The TCA cycle and the ETC
    2. Glycolysis and ETC
    3. Gluconeogenesis and Krebs Cycle
    4. Glycogenolysis and ETC
A

a. The TCA cycle and the ETC

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14
Q
  1. In glycolysis how many pyruvate molecules are produced from each glucose molecule? (slide 21)
    1. 1
    2. 2
    3. 3
    4. None
A

b. 2

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15
Q
  1. Which molecule enters the mitochrondria and the TCA cycle? (slide 27)
    1. Glucose
    2. Glycogen
    3. Pyruvic acid
    4. Lactic acid
A

c. Pyruvic acid

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16
Q
  1. What is gluconeogenesis? (slide 29)
    1. The synthesis of glucose from non carbohydrate precursors
    2. The synthesis of glucose from fats
    3. The synthesis of glycogen
    4. The synthesis of glycogen specifically from fats
A

a. The synthesis of glucose from non carbohydrate precursors

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17
Q
  1. What is glycogensis? (slide 29)
    1. The synthesis of glucose from non carbohydrate precursors
    2. The synthesis of glucose from fats
    3. The synthesis of glycogen
    4. The synthesis of glycogen specifically from fats
A

c. The synthesis of glycogen

18
Q
  1. What is the breakdown of lipids known as? (slide 32)
    1. Lipolysis
    2. Lipogenesis
    3. Glycerolysis
    4. Glycolysis
A

a. Lipolysis

19
Q
  1. Fatty acids are broken down in the mitochondrion in which metabolic pathway? (slide 32)
    1. Electron transport chain
    2. TCA cycle
    3. Beta-oxidation
    4. Citric acid cycle
A

c. Beta-oxidation

20
Q
  1. Linoleic acid is an example of what? (slide 34)
    1. An essential fatty acid
    2. A non-essential fatty acid
    3. An essential amino acid
    4. A non-essential amino acid
A

a. An essential fatty acid

21
Q
  1. What is a lipoprotein? (slide 35)
    1. A fatty protein
    2. A lipid-protein complex
    3. A protein stored in subcutaneous fat
    4. A fatty acid stored in muscle tissue
A

b. A lipid-protein complex

22
Q
  1. How many classes of lipoprotein are there? (slide 35)
    1. 1
    2. 2
    3. 5
    4. 10
A

c. 5

23
Q
  1. What is the name of the enzyme that breaks down complex lipids? (slide 36)
    1. Liporotein lipase
    2. Protolipid lipase
    3. Lipoprotein acid
    4. Lipoprotein hormone
A

a. Liporotein lipase

24
Q
  1. What do chylomicrons do? (slide 35)
    1. Transport glucose from the gut
    2. Transport amino acids from the gut
    3. Transport lipids from the gut
    4. Transport enzymes from the gut
A

c. Transport lipids from the gut

25
Q
  1. Roughly how many amino acids does the body use? (slide 39)
    1. 5
    2. 10
    3. 20
    4. 40
A

c. 20

26
Q
  1. The amino acids the body cannot make are known as what? (slide 39)
    1. Emergency amino acids
    2. Important amino acids
    3. Redundant amino acids
    4. Essential amino acids
A

d. Essential amino acids

27
Q
  1. If proteins are metabolised, what is the first group removed? (slide 40)
    1. Amino group
    2. Carboxyllic group
    3. R group
    4. Hydroxyl
A

a. Amino group

28
Q
  1. Once the group has been removed which of the following occurs? (slide 41)
    1. They are merged to make longer carbon chains
    2. The double bonds are broken to release energy
    3. They are broken down to small carbon chain molecules
    4. Surplus nitrogen is removed
    5. They are oxidised in the cori cycle
A

c. They are broken down to small carbon chain molecules

29
Q
  1. Where does protein synthesis occur? (slide 43)
    1. In the nucleus
    2. On the ribosomes
    3. In the mitochondria
    4. In the cytoplasm
A

b. On the ribosomes

30
Q
  1. Which of the following is true? C = carbohydrate, F = fat (slide 45)
    1. C can be converted into F, F can be converted into C
    2. C cannot be converted into F, but F can be converted into C
    3. C cannot be converted into F and F cannot be converted into F
    4. C can be converted into F but F cannot be converted into C
A

d. C can be converted into F but F cannot be converted into C

31
Q
  1. Nucelic acids contribute significantly to energy reserves. (slide 47)
    1. True
    2. False
A

b. False

32
Q
  1. Metabolic activities require coordination: (slide 49)
    1. Over time
    2. Over space
    3. Over time and space
A

c. Over time and space

33
Q
  1. Which of the following is a focal point for metabolic regulation and control? (slide 50)
    1. The liver
    2. Adipose tissue
    3. The endocrine system
    4. The kidneys
A

a. The liver

34
Q
  1. Which is the only substrate that can be used by neural tissue? (slide 50)
    1. Lipids
    2. Amino acids
    3. Glucose
    4. Glycogen
A

c. Glucose

35
Q
  1. What do adipocytes store? (slide 51)
    1. Triglyceride
    2. Amino acids
    3. Glycogen
    4. Free fatty acids
A

a. Triglyceride

36
Q
  1. Carbohydrates are stored as (slide 51)
    1. Glycogen
    2. Glucose
    3. Triglycerides
    4. Glycogen and/or fat
A

d. Glycogen and/or fat

37
Q
  1. The uptake and storage of energy substrates are stimulated by what hormone? (slide 52)
    1. Insulin
    2. Glucagon
    3. Oxytoxin
    4. Ghrelin
A

a. Insulin

38
Q
  1. What is the ‘absorptive’ state? (slide 51)
    1. The period immediately following a meal
    2. The period before a meal
    3. The period between meals
A

a. The period immediately following a meal

39
Q
  1. Which substrate forms the biggest reserve?
    1. Lipids
    2. Proteins
    3. Carbohydrates
A

a. Lipids

40
Q
  1. Why are glycogen stores important? (slide 54)
    1. They are readily accessible
    2. They are very compact
    3. They are slow to reabsorb
    4. They are only stored in the muscle
A

a. They are readily accessible