A. HMG-Co A synthase
B. Malic enzyme
C. Malonyl CoA synthetase
D. Fatty acid synthetase
Related Mcqs:
- 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 - Acetyl CoA is produced from which fuel sources_____________?
A. Carbohydrate
B. Lipid
C. Amino acids
D. All of the above - One molecule of acetyl Co-A gives rise to ________ ATP molecules?
A. 2
B. 8
C. 12
D. 32 - What high energy phosphate compound is formed in the citric acid cycle through substrate level phosphorylation______________?
A. ATP
B. TTP
C. ITP
D. GTP - In TCA cycle substrate level phosphorylation occurs at____________?
A. Succinate dehydrogenase
B. Malonate reduction
C. Thiokinase
D. None of the above - 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 - Enzymes concerned with the citric acid cycle are found in______________?
A. Nucleus
B. Mitochondria
C. Ribosomes
D. Non-particulate cytoplasm - Enzymes help by____________?
A. Lowering the activation energy
B. Increasing the substrate concentration
C. Decreasing the surface tension
D. Increasing the activation energy - Inactive precursors of enzymes are known as_______________?
A. Apoenzymes
B. Coenzymes
C. Proenzymes
D. Holoenzymes - Mutation in the oxidative enzymes (peroxisomes) could lead to_______________?
A. Zellweger’s syndrome
B. Gaucher’s disease
C. Epidermolysis bullosa
D. Leber’s neuropathy