1. Neutral amino acid is Arginine Lysine Aspartate Leucine 2. Methionine is synthesised from Glycine Cysteine Arginine Histidine 3. Glucose 6 phosphatase deficicency is seen in Von gierke’s disease Pompe’s disease Downs syndrome McArdles syndrome 4. eukayotic plasma membrane is made up of all except triglycerides carbohydrates cholesterol lecithin 5. all the statements regarding LDL receptors are true except it is taken into the cells by endocytosis clathrin-coated pits contain the receptor on cell membranes increased cellular cholesterol down regulates the synthesis of LDL receptors present only in extra-hepatic tissues 6. Transport proteins are Globular proteins Fibrous proteins Bulky proteins Threaded proteins 7. Both ketogenic and glucogenic amino acid is Isoleucine Glycine leucine Arginine 8. the major fate of glucose -6 phosphate in tissue in a well fed state is conversion to ribulose 5 phosphate hydrolysis to glucose conversion to glycogen isomerisation to fructose 6 phosphate 9. starting material for production of insulin from bacteria is genomic DNA from lymphocytes of human mRNA from lymphocytes of human mRNA from beta pancreatic cells of human genomic DNA from beta pancreatic cells of human 10. The citric acid cycle is the final pathway for oxidation of Vitamins None of the above Minerals Enzymes 11. thiamine requirement increase in excessive intake of lecithine carbohydrates fat amino acid 12. in well fed state, the activity of CPT-1(Carnitine palmitoyl transferase) in outer mitochondrial membrane is inhibited by glucose acetyl CoA malonyl CoA pyruvate 13. Thiamine deficiency causes decreased energy production because It is a co-factor in oxidative reduction It is required for the process of transamination It is co-enzyme for pyruvate dehydrogenase It is co-enzyme for transketolase in pentose phosphate pathway 14. Storage form of free energy in the cell is- Creatine phosphate ATP NADH G-6-P 15. Albumin and globulin are classified as Simple globular proteins Conjugated proteins Unconjugated proteins Derived proteins 16. the defect in xeroderma pigmentosa is formation of adenine dimers exonuclease is defective poly ADP ribose polymerase is defective formation of thymidine dimmers 17. during phagocytosis the metabolic process called respiratory burst involves the activation of hydrolase oxidase peroxidise dehydrogenase 18. Fructose 2-6 bisphosphate regulates glycolysis at the level of Phosphoenol pyruvate Glyceraldehyde 3 phosphate Fructose 6 phosphate Glucose 6 phosphate 19. collagen is rich in proline and glycine glutamate and glycine glutamate and proline alanine and glycine 20. Which of the following is a salivary enzyme Lactase Maltase Amylase Lipase Loading … Question 1 of 20
