A. 2
B. 36
C. 38
D. 32
Related Mcqs:
- One molecule of acetyl Co-A gives rise to ________ ATP molecules?
A. 2
B. 8
C. 12
D. 32 - An essential for the conversion of glucose to glycogen in liver is____________?
A. UTP
B. GTP
C. Pyruvate Kinase
D. Guanosine - Increase in pyruvate and lactate is seen in which of the following deficiency ?
A. Thiamine
B. Pyridoxine
C. Niacin
D. Vitamin C - Increase in lactate and pyruvate is seen in deficiency of_____________?
A. Pyridoxin
B. Niacin
C. Thiamine
D. Retinotic acid - Lactate dehydrogenase is____________?
A. Isozyme
B. Coenzyme
C. Antienzyme
D. Zymogen - In glycolysis ATP is produced by the following enzyme______________?
A. Hexokinase
B. Phosphoglycerate kinase
C. Enolase
D. Phosphohexose isomerase - In which type of glycogen storage disease is hyper uricemia a feature ?
A. I
B. II
C. III
D. IV - Blood glucose level cannot be augmented by mobilization of muscle glycogen due to lack of_____________?
A. G-6-P dehydrogenase
B. G-6-P phydrogenase
C. Aldolase
D. Glucokinase - Glycogen breakdown leads to formation of______________?
A. Glucose
B. Lactic acid
C. Glucose & Lactic acid
D. Glycoprotein - Type II glycogen storage disorder is due to deficiency of______________?
A. Alpha -Glucosidase
B. Alpha galactosidase
C. Muscle phosphorylase
D. Acid Lipase