A. HMG-Co A synthase
B. Malic enzyme
C. Malonyl CoA synthetase
D. Fatty acid synthetase

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Related Mcqs:

  1. Which one of the following is the correct sequential order in which the given enzymes of kreb’s cycle are formed after a molecule of acetyl CoA______________?
    A. Citrate, Oxalocetate, Ketoglutarate B. Ketoglutarate, Oxalocetate, Citrate C. Citrate, Ketoglutarate, Oxalocetate D. Oxalocetate, Ketoglutarate, Citrate...
  2. Acetyl CoA is produced from which fuel sources_____________?
    A. Carbohydrate B. Lipid C. Amino acids D. All of the above...
  3. One molecule of acetyl Co-A gives rise to ________ ATP molecules?
    A. 2 B. 8 C. 12 D. 32...
  4. What high energy phosphate compound is formed in the citric acid cycle through substrate level phosphorylation______________?
    A. ATP B. TTP C. ITP D. GTP...
  5. In TCA cycle substrate level phosphorylation occurs at____________?
    A. Succinate dehydrogenase B. Malonate reduction C. Thiokinase D. None of the above...
  6. In TCA, substrate level phospherylation takes place in______________?
    A. Alpha ketoglutrate to succinyl CoA B. Succinyl CoA to Succinate C. Succinate to fumarate D. Oxalocetate to citrate...
  7. Enzymes concerned with the citric acid cycle are found in______________?
    A. Nucleus B. Mitochondria C. Ribosomes D. Non-particulate cytoplasm...
  8. Enzymes help by____________?
    A. Lowering the activation energy B. Increasing the substrate concentration C. Decreasing the surface tension D. Increasing the activation energy...
  9. Inactive precursors of enzymes are known as_______________?
    A. Apoenzymes B. Coenzymes C. Proenzymes D. Holoenzymes...
  10. Mutation in the oxidative enzymes (peroxisomes) could lead to_______________?
    A. Zellweger’s syndrome B. Gaucher’s disease C. Epidermolysis bullosa D. Leber’s neuropathy...
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