Breaking News

BIO CHEMISTRY MCQs (PART 3) by General knowledge Solutions

BIO CHEMISTRY MCQs (PART3)  by General knowledge Solutions





1. Cerebrosides contain all the following except

  • (A) Galactose
  • (B) Sulphate
  • (C) Sphingosine
  • (D) Fatty acid


 2. Niemann-Pick disease results from deficiency of

  • (A) Ceramidase
  • (B) Sphingomyelinase
  • (C) Arylsulphatase A
  • (D) Hexosaminidase A


3. Chylomicron remnants are catabolised in

  • (A) Intestine
  • (B) Adipose tissue
  • (C) Liver
  • (D) Liver and intestine


4. VLDL remnant may be converted into

  • (A) VLDL
  • (B) LDL
  • (C) HDL
  • (D) Chylomicrons


5. Receptors for chylomicron remnants are

  • (A) Apo A specific
  • (B) Apo B-48 specific
  • (C) Apo C specific
  • (D) Apo E specific


6. LDL receptor is specific for

  • (A) Apo B-48 and Apo B 100
  • (B) Apo B-48 and Apo E
  • (C) Apo B-100 and Apo D
  • (D) Apo B-100 and apo D


7. Nascent HDL of intestinal origin lacks

  •  (A) Apo A
  • (B) Apo C
  • (C) Apo E
  •  (D) Apo C and Apo E


8. HDL is synthesized in

  •  (A) Adipose tissue
  • (B) Liver
  • (C) Intestine
  • (D) Liver and intestine


9. Nascent HDL of intestinal origin acquires Apo C and Apo E from

  • (A) Chylomicrons
  • (B) VLDL
  • (C) LDL
  • (D) HDL of the hepatic origin


10. Heparin releasable hepatic lipase converts

  • (A) VLDL remnants into LDL
  • (B) Nascent HDL into HDL
  • (C) HDL2 into HDL3
  • (D) HDL3 into HDL2


 11. Activated lecithin cholesterol acyl transferase is essential for the conversion of

  • (A) VLDL remnants into LDL
  • (B) Nascent HDL into HDL
  • (C) HDL2 into HDL3
  • (D) HDL3 into HDL2


 12. Fatty liver may be caused by

  • (A) Deficiency of methionine
  • (B) Puromycin
  • (C) Chronic alcoholism
  • (D) All of these


 13. Alcohol dehydrogenase converts ethanol into

  • (A) Acetyl CoA
  • (B) Acetaldehyde
  • (C) Acetate
  • (D) CO2 and H2O


14. Lipids are stored in the body mainly in the form of

  • (A) Phospholipids
  • (B) Glycolipids
  • (C) Triglycerides
  • (D) Fatty acids


15. Lipid stores are mainly present in

  • (A) Liver
  • (B) Brain
  • (C) Muscles
  • (D) Adipose tissue


 16. Glycerol is converted into glycerol-3- phosphate by

  • (A) Thiokinase
  • (B) Triokinase
  • (C) Glycerol kinase
  •  (D) All of these


17. In adipose tissue, glycerol-3-phosphate required for the synthesis of triglycerides comes mainly from

  • (A) Hydrolysis of pre-existing triglycerides
  • (B) Hydrolysis of phospholipids
  • (C) Dihydroxyacetone phosphate formed in glycolysis
  • (D) Free glycerol


18. Glycerol released from adipose tissue by hydrolysis of triglycerides is mainly

  • (A) Taken up by liver
  • (B) Taken up by extrahepatic tissues
  • (C) Reutilised in adipose tissue
  • (D) Excreted from the body

19. Free glycerol cannot be used for triglyceride synthesis in

  • (A) Liver
  • (B) Kidney
  • (C) Intestine
  • (D) Adipose tissue


 20. Adipose tissue lacks

  • (A) Hormone-sensitive lipase
  • (B) Glycerol kinase
  • (C) cAMP-dependent protein kinase
  • (D) Glycerol-3-phosphate dehydrogenase


21. A digestive secretion that does not contain any digestive enzyme is

  • (A) Saliva
  • (B) Gastric juice
  • (C) Pancreatic juice
  • (D) Bile


 22. Saliva contains a lipase which acts on triglycerides having

  • (A) Short chain fatty acids
  • (B) Medium chain fatty acids
  • (C) Long chain fatty acids
  • (D) All of these


23. Salivary lipase hydrolyses the ester bond at

  • (A) Position 1 of triglycerides
  • (B) Position 2 of triglycerides
  •  (C) Position 3 of triglycerides
  •  (D) All of these


 24. Salivary lipase converts dietary triglycerides into

  • (A) Diglycerides and fatty acids
  • (B) Monoglycerides and fatty acids
  • (C) Glycerol and fatty acids
  • (D) All of these



25. Pancreatic lipase requires for its activity:

  • (A) Co-lipase
  • (B) Bile salts
  • (C) Phospholipids
  • (D) All of these


 26. Pancreatic lipase converts triacylglycerols into

  • (A) 2, 3-Diacylglycerol
  • (B) 1-Monoacylglycerol
  • (C) 2-Monoacylglycerol
  • (D) 3-Monoacylglycerol


 27. Oxidation of fatty acids occurs

  • (A) In the cytosol
  • (B) In the matrix of mitochondria
  • (C) On inner mitochondrial membrane
  • (D) On the microsomes


28. Activation of fatty acids requires all the following except

  • (A) ATP
  • (B) Coenzyme A
  • (C) Thiokinase
  • (D) Carnitine


 29. Mitochondrial thiokinase acts on

  • (A) Short chain of fatty acids
  • (B) Medium chain fatty acids
  • (C) Long chain fatty acids
  • (D) All of these


 30. Carnitine is required for the transport of

  • (A) Triglycerides out of liver
  • (B) Triglycerides into mitochondria
  • (C) Short chain fatty acids into mitochondria
  • (D) Long chain fatty acids into mitochondria


31. Carnitine acylcarnitine translocase is present

  • (A) In the inner mitochondrial membrane
  • (B) In the mitochondrial matrix
  • (C) On the outer surface of inner mitochondrial membrane
  • (D) On the inner surface of inner mitochondrial membrane


 32. Net ATP generation on complete oxidation of stearic acid is

  • (A) 129
  • (B) 131
  • (C) 146
  • (D) 148


33. Propionyl CoA formed oxidation of fatty acids having an odd number of carbon atoms is converted into

  • (A) Acetyl CoA
  • (B) Acetoacetyl CoA
  •  (C) D-Methylmalonyl CoA
  • (D) Butyryl CoA


34. α-Oxidation of fatty acids occurs mainly in

  • (A) Liver
  • (B) Brain
  • (C) Muscles
  • (D) Adipose tissue

35. Refsum’s disease results from a defect in the following pathway except

  •  (A) Alpha-oxidation of fatty acids
  •  (B) Beta-oxidation of fatty acids
  •  (C) Gamma-oxidation of fatty acids
  •  (D) Omega-oxidation of fatty acids


 36. The end product of omega-oxidation of fatty acids having an even number of carbon atoms is

  •  (A) Adipic acid
  •  (B) Suberic acid
  •  (C) Both (A) and (B)
  •  (D) None of these


37. De novo synthesis of fatty acids is catalysed by a multi-enzyme complex which contains

  • (A) One-SH group
  • (B) Two-SH groups
  • (C) Three-SH groups
  • (D) Four-SH groups


39. Fat depots are located in

  • (A) Intermuscular connective tissue
  • (B) Mesentary
  • (C) Omentum
  • (D) All of these


40. Salivary lipase is secreted by

  •  (A) Parotid glands
  •  (B) Sub-maxillary glands
  •  (C) Dorsal surface of tongue
  •  (D) None of these


41. Co-lipase is a

  • (A) Bile salt
  • (B) Vitamin
  • (C) Protein
  • (D) Phospholipid


42. Plasma becomes milky

  • (A) Due to high level of HDL
  • (B) Due to high level of LDL
  • (C) During fasting
  • (D) After a meal


 43. Mitochondrial membrane is permeable to

  •  (A) Short chain fatty acids
  •  (B) Medium chain fatty acids
  •  (C) Long chain fatty acids
  •  (D) All of these


44. During each cycle of β-oxidation

  •  (A) One carbon atom is removed from the carboxyl end of the fatty acid
  •  (B) One carbon atom is removed from the methyl end of the fatty acid
  •  (C) Two carbon atoms are removed from the carboxyl end of the fatty acid
  •  (D) Two carbon atoms are removed from the methyl end of the fatty acid


 45. Net generation of energy on complete oxidation of palmitic acid is

  • (A) 129 ATP equivalents
  • (B) 131 ATP equivalents
  • (C) 146 ATP equivalents
  • (D) 148 ATP equivalents


 46. Net generation of energy on complete oxidation of a 17-carbon fatty acid is

  • (A) Equal to the energy generation from a 16-carbon fatty acid
  • (B) Equal to the energy generation from an 18-carbon fatty acid
  • (C) Less than the energy generation from a 16-carbon fatty acid
  • (D) In between the energy generation from a 16-carbon fatty acid and an 18-carbon fatty acid


 47. Net energy generation on complete oxidation of linoleic acid is

  • (A) 148 ATP equivalents
  • (B) 146 ATP equivalents
  • (C) 144 ATP equivalents
  • (D) 142 ATP equivalents


 48. Extramitochondrial synthesis of fatty acids occurs in

  • (A) Mammary glands
  • (B) Lungs
  • (C) Brain
  • (D) All of these


 49. One functional sub-unit of multi-enzyme complex for de novo synthesis of fatty acids contains

  •  (A) One —SH group
  •  (B) Two —SH groups
  •  (C) Three —SH groups
  •  (D) Four —SH groups

No comments