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Amino Acid Metabolism MCQ Questions & Answers

Amino Acid Metabolism MCQs : This section focuses on the "Amino Acid Metabolism". These Multiple Choice Questions (MCQs) should be practiced to improve the Amino Acid Metabolism skills required for various interviews (campus interview, walk-in interview, company interview), placement, entrance exam and other competitive examinations.




Question 1

Oxidative deamination is the conversion of an amino

A. group from an amino acid to a keto acid
B. acid to a carboxylic acid plus ammonia
C. acid to a keto acid plus ammonia
D. group from an amino acid to a carboxylic acid

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Question 2

Transamination is the transfer of an amino

A. acid to a carboxylic acid plus ammonia
B. group from an amino acid to a keto acid
C. acid to a keto acid plus ammonia
D. group from an amino acid to a carboxylic acid

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Question 3

An example of a transamination process is

A. glutamate = hexanoic acid + NH3
B. aspartate + hexanoic acid = glutamate + oxaloacetate
C. aspartate + α ketoglutarate = glutamate + oxaloacetate
D. glutamate = α-ketoglutarate + NH3

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Question 4

A person with phenylketonuria is advised not to consume which of the following products?

A. Glycine containing foods
B. Fat containing food
C. Glucose
D. Aspartame

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Question 5

An example of the oxidative deamination is

A. glutamate = hexanoic acid + NH3
B. aspartate + α-ketoglutarate = glutamate + oxaloacetate
C. glutamate = α-ketoglutarate + NH3
D. aspartate + hexanoic acid = glutamate + Oxaloacetate

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Question 6

Transaminase enzymes are present in

A. liver
B. pancreas
C. intestine
D. none of these

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Question 7

Histidine is degraded to α-ketoglutarate and is described as a

A. gluco amino acid
B. glucogenic amino acid
C. ketogenic amino acid
D. keto-gluco amino acid

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Question 8

Tyrosine is degraded to acetoacetyl CoA and fumarate and is described as a

A. glucogenic amino acid
B. ketogenic amino acid
C. ketogenic and glucogenic amino acid
D. keto-gluco amino acid

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Question 9

Lysine is degraded to acetoacetyl CoA and is described as a

A. ketogenic amino acid
B. glucogenic amino acid
C. keto-gluco amino acid
D. none of these

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Question 10

Which of the following amino acids is considered as both ketogenic and glucogenic?

A. Valine
B. Tryptophan
C. Lysine
D. None of these

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Question 11

The most toxic compounds is

A. tyrosine
B. phenylpyruvate
C. lysine
D. phenylalanine

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Question 12

In the normal breakdown of phenylalanine, it is initially degraded to

A. fumarate
B. tyrosine
C. lysine
D. phenylpuruvate

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Question 13

A person with phenylketonuria cannot convert

A. phenylalanine to tyrosine
B. phenylalanine to isoleucine
C. phenol into ketones
D. phenylalanine to lysine

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Question 14

A person with phenylketonuria will convert

A. phenylalanine to phenylpyruvate
B. phenylalanine to isoleucine
C. phenylpyruvate to phenylalanine
D. tyrosine to phenylalanine

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Question 15

Transamination is the process where

A. carboxyl group is transferred from amino acid
B. α-amino group is removed from the amino acid
C. polymerisation of amino acid takes place
D. none of the above

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Question 16

A glucogenic amino acid is one which is degraded to

A. keto-sugars
B. either acetyl CoA or acetoacetyl CoA
C. pyruvate or citric acid cycle intermediates
D. none of the above

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Question 17

A ketogenic amino acid is one which degrades to

A. keto-sugars
B. either acetyl CoA or acetoacetyl CoA
C. pyruvate or citric acid cycle intermediates
D. multiple intermediates including pyruvate or citric acid cycle intermediates and acetyl CoA or acetoacetyl CoA

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Question 18

A person suffering from phenylketonuria on consumption food containing high phenylalanine may lead to the accumulation of

A. phenylalanine
B. phenylpyruvate
C. tyrosine
D. isoleucine

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Question 19

Which of the following is the best described glucogenic amino acid?

A. Lysine
B. Tryptophan
C. Valine
D. None of these

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Question 20

A best described ketogenic amino acid is

A. lysine
B. tryptophan
C. valine
D. none of these

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Question 21

In which form the nitrogen is incorporated into an amino acid?

A. Nitrite
B. Glutamate
C. Nitrate
D. Ammonium ion

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Question 22

Intermediates of which of the following metabolic pathway have not been used in the synthesis of amino acids?

A. Glycolysis
B. Fatty acid biosynthesis
C. Citric acid cycle
D. Pentose phosphate pathway

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Question 23

Name those living organisms which secrete nitrogen in the form of urea?

A. Ureotelic
B. Uricotelic
C. Ammonotelic
D. Nitroso compounds

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Question 24

Name the type of cell in which synthesis of urea cycle takes place?

A. Pancreatic cell
B. Hepatocyte
C. Bowman’s gland cell
D. Urinary epithelium cell

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Question 25

The urea cycle is also referred to as Krebs-Henseleit cycle.

A. True
B. False

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Question 26

Transamination reaction in amino acid synthesis is catalyzed by enzyme_________

A. Nitric oxide synthase
B. Decarboxylase
C. Aminotransferase
D. Glutamate decarboxylase

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Question 27

Which of the following is non-essential amino acid?

A. Lysine
B. Leucine
C. Serine
D. Methionine

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Question 28

Which of these amino acids are essential for infants?

A. Methionine
B. Arginine and Histidine
C. Valine
D. Lysine and Leucine

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Question 29

Which of these is a hereditary disease caused due to an error in amino acid metabolism?

A. Homocystinuria
B. Albinism
C. Phenylketonuria
D. Branched-chain ketoaciduria

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