The correct answers for
9. PEP carboxykinase does not require biotin as coenzyme.
10. The source of acetyl-SCoA in the cytoplasm is citrate.
It is catalyzed by an enzyme ATP citrate lyase which is located in the cytoplasm.
9. Which of the listed enzymes does not require biotin as coenzyme ?: a pyruvate carboxylase b. a...
11. Name the enryme catalyzing the following reaction a pyruvate carboxylase b propionyl-SCoA carboxylase c. PEP carbosylase d acetyl-SCoA carboxylase citae
9. Which of the listed enzymes of the TCA cycle is regulated by phosphorylation/dephosphorylation cycle ? :a. isocitrate dehydrogenase b. succinate dehydrogenase c. malate dehydrogenase d. α-ketoglutarate dehydrogenase complex\}c. citrate synthase10. Name the enzyme catalyzing the following reaction:a. PEP carboxykinaseb. pyruvate kinasec. malic enzymed. pyruvate carboxylase11. Name the enzyme that catalyzes the reaction:glyoxylate +CH3CO-SCoA → malate + HSCoAa. malate synthaseb. succinate thiokinasec. aconitased. isocitrate
9. Which of the listed enzymes of the TCA cycle is regulated by phosphorylation/dephosphorylation cycle ? : a. isocitrate dehydrogenase b. succinate dehydrogenase c. malate dehydrogenase d. a-ketoglutarate dehydrogenase complex e. citrate synthase 10. Name the enzyme catalyzing the following reaction: COOH + GTP - PEP + CO2 + GDP C=0 CH2 COOH a. PEP carboxykinase b. pyruvate kinase d. pyruvate carboxylase c. malic enzyme 11. Name the enzyme that catalyzes the reaction: glyoxylate + CH3CO-SCOA -- → malate +...
15. Genetic defect in pyruvate dehydrogenase complex lead a. maple syrup urine disease b. phenyike d. lactic acidemia e. pellagra syrup urine disease b, phenylketonuria c. galactosemia 10. Chemical modification by phosphorylation of pyruvate dehydros a. deactivates the enzyme b. activates the enzyme lation of pyruvate dehydrogenase complex : 17. Pyruvate carboxylase is positively ated through the allosteric mechanism by : a. ATP b. NADH c. Acetyl-SCOA d. TPP e. Biotin 18. Which of the listed coenzymes does not particip...
1. Which enzyme is NOT part of the GNG process? a .Pyruvate kinase b. Pyruvate carboxylase c. Phosphoenolpyruvate carboxykinsase d. Glucose-6-phosphatase 2. Which molecule can NOT be derived from pyruvate in human? a. Oxaloacetate b. Acetyl CoA c. Lactate d. Ethanol 3. Which one of the following statements regarding the ruminant gluconeogenesis process is correct? a. It leads to net gain of ATP. b. It begins with propionate. c. It begins with lactate. d. It begins with pyruvate.
QUESTION 4 Which of the following enzymes directly converts phosphorylaseb into the more active form, phosphorylase a? A. CAMP-dependent protein kinase B. phosphorylase kinase C. protein kinase A D. adenylate kinase E phosphoprotein phosphatase The biotin prosthetic group of pyruvate carboxylase is covalently attached to a residue of the enzyme ? A. Vakine B. serine C. lysine D. arginine E. the biotin is attached non-covalently Which of the following serves as the energy source for the metabolic conversion of oxaloacetate...
I1. Mammals lack the enzyme a. Lactate dehydrogenase b. Pyruvate kinase Alcohol Dehydrogenase c. d. Pyruvate decarboxylase None of the above are correct e. 12. The first reaction of the Krebs cycle combines Oxaloacetate and Acetyl CoA to make Citrate b. a. Malate and NADH to make Citrate a-ketoglutarate and citrate to make CO2 d. c- Succinate and Citrate to make Oxaloacetate 13. The electrons held by NADH and FADH, are donated to the which complexes in the ETC respectively?...
Can someone quick answer/check these questions? Thank you, will rate! (the answers that I have came up with are in bold) Please help 51- Glycogenesis involves the following steps a) isomerisation b) activation c) elongation or coupling d) branching e) all of the above 52 During the breakdown of glycogen, free glucose is formed from A. the reducing end. B. the non-reducing end. C. glucose residues in an a 1-->4 linkage to the chain. D. glucose residues in an...
The primary regulatory point of gluconeogenesis is____? a. glucose-6-phosphatase b. fructose-1,6-biphosphatase c. fuctose-2,6-biphosphatase d. pyruvate carboxylase (wrong answer) e. PEP carboxykinase Please explain why pyruvate carboxylase is wrong (isn't it one of the regulatory points, is it wrong because it isn't the primary one? and if so, how do you know what the primary one is?) and state the right answer and an explanation as to why.
Which enzymes require thiamine as a co-factor A. Isocitrate dehydrogenase and citrate synthase B. Malate dehydrogenase and alpha-ketoglutarate dehydrogenase C. Pyruvate dehydrogenase and isocitrate dehydrogenase D. Pyruvate dehydrogenase and succinyl-CoA synthetase E. Succinate dehydrogenase and pyruvate dehydrogenase