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Respiration in Plants Test - 2

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Respiration in Plants Test - 2
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  • Question 1
    1 / -0

    In TCA cycle, all of the following are the products of oxidation reaction, except

    Solution

     

    α-Ketoglutarate is produced from decarboxylation of oxalosuccinate by isocitrate dehydrogenase.

  • Question 2
    1 / -0

    State true (T) or false (F) for the following sentences:

    1. A small quantity of oxygen enhances fermentation.
    2. Water molecule is released in acetic acid fermentation.
    3. Ethyl alcohol is the byproduct of lactic acid fermentation.
    4. Yeast cells prefer aerobic respiration in presence of abundant oxygen

    Solution

     

    Presence of trace quantities of oxygen increases the rate of fermentation. Water molecule is released in Butyric acid fermentation. Ethyl alcohol is a byproduct of lactic acid fermentation by lactic acid bacteria. Yeast cells greatly prefer fermentation to aerobic respiration in presence of abundant oxygen.

  • Question 3
    1 / -0

    Which of the following enzymes act in pentose phosphate pathway?

    a. Hexokinase
    b. Aconitase
    c. Isomerase
    d. Carboxylase
    e. Transketolase

    Solution

    Enzymes isomerase and transketolase participate in pentose phosphate pathway. Isomerase produces ribose-5-phosphate and xylulose-5-phosphate from ribulose-5-phosphate. Transketolase acts on sedoheptulose-7-phosphate to produce fructose-6-phosphate and erythrose-4-phosphate. Transketolase also acts upon erythrose-4-phosphate and xylulose-5-phosphate and yields fructose-6-phosphate and glyceraldehyde-3-phosphate.

  • Question 4
    1 / -0

    Conversion of pyruvic acid into acetyl CoA yields energy in the form of

    Solution

     

    Conversion of pyruvic acid into acetyl CoA yields energy in the form of NADH, which is equivalent to 3 ATP.

  • Question 5
    1 / -0

    The activity of which of the following enzymes of pentose phosphate pathway can be decreased by thiamine deficiency?

    Solution

    Transketolase activity is decreased by deficiency of thiamine. The co-factor thiamine diphosphate accepts a 2-carbon fragment from a 5-carbon ketose (D-xylulose-5-P), then transfers this fragment to a 5-carbon aldose (D-ribose-5-P) to form a 7-carbon ketose (sedoheptulose-7-P). In another reaction catalysed by transketolase i.e., transfer of a 2-carbon fragment from D-xylulose-5-P to the aldose erythrose-4-phosphate, thiamine acts as a co-factor.

  • Question 6
    1 / -0

    α-Ketoglutarate, an intermediate of Krebs cycle, provides the carbon skeleton for synthesis of all, except

    Solution

    Oxaloacetate provides the carbon skeleton for synthesis of asparagine. Alpha-ketoglutarate forms glutamine, proline, and arginine.

  • Question 7
    1 / -0

    Phosphoglucoisomerase is an enzyme associated with the glycolytic pathway. Which of the following is the product of this enzyme?

    Solution

    Phosphoglucoisomerase (alternatively known as phosphoglucose isomerase or Glucose-6-phosphate isomerase) are a group of enzymes of the isomerase family (EC 5.3.1.9), so named for their main function in glycolysis and gluconeogenesis.Phosphoglucose isomerase (PGI) produces β-D Fructose 6-phosphate from α-D-Glucose 6-phosphate. The proposed reaction mechanism of PGI for the reversible conversion of glucose-6-phosphate to fructose 6-phosphate involves an acid/base catalysis by the enzyme. The basic mechanism involves the isomerization of an aldose to a ketose.

  • Question 8
    1 / -0

    Ubiquinone is a coenzyme. It is required for the activity of

    Solution

    Ubiquinone is a coenzyme required for the activity of succinate dehydrogenase. Succinate dehydrogenase catalyses the conversion of succinate to fumarate.

  • Question 9
    1 / -0

    Which of the following is/are not produced from two acetyl-CoA molecules at the end of Kreb's cycle?

    Solution

    One GTP molecule is produced from one acetyl-CoA molecules. Two GTP molecules are produced from two acetyl-CoA molecules.

  • Question 10
    1 / -0

    Which of the following glycolytic enzymes is associated with glycogen storage disease type 1 in humans?

    Solution

    Glycogen storage disease is a genetic disease which results from deficiency of the enzyme glucose-6-phosphatase. The deficiency impairs the ability of the liver to produce free glucose from glycogen and from gluconeogenesis.

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