In ornithine cycle, enzyme arginase breaks down arginine into

In ornithine cycle, enzyme arginase breaks down arginine into
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In ornithine cycle, enzyme arginase breaks down arginine into A. Citrulline and ammonia B. Ornithine ... C. Ornithine and urea D. Citruline and urea
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Control of urea cycle involves the enzyme: (A) Carbamoyl phosphate synthetase (B) Ornithine transcarbamoylase (C) Argininosuccinase (D) Arginase

Description : Control of urea cycle involves the enzyme: (A) Carbamoyl phosphate synthetase (B) Ornithine transcarbamoylase (C) Argininosuccinase (D) Arginase

Last Answer : Answer : A

Hyperargininemia, a defect in urea synthesis develops due to deficiency of the enzyme: (A) Ornithine transcarbamoylase (B) Argininosuccinase (C) Arginase (D) Argininosuccinate synthetase ENZYMES 157

Description : Hyperargininemia, a defect in urea synthesis develops due to deficiency of the enzyme: (A) Ornithine transcarbamoylase (B) Argininosuccinase (C) Arginase (D) Argininosuccinate synthetase ENZYMES 157

Last Answer : Answer : B

In urea synthesis, the amino acid functioning solely as an enzyme activator: (A) N-acetyl glutamate(B) Ornithine (C) Citrulline (D) Arginine

Description : In urea synthesis, the amino acid functioning solely as an enzyme activator: (A) N-acetyl glutamate(B) Ornithine (C) Citrulline (D) Arginine

Last Answer : Answer : A

The following 4 amino acids are required for completion of urea cycle except (A) Aspartic acid (B) Arginine (C) Ornithine (D) Glycine

Description : The following 4 amino acids are required for completion of urea cycle except (A) Aspartic acid (B) Arginine (C) Ornithine (D) Glycine

Last Answer : Answer : D

An amino acid not involved in urea cycle is (A) Arginine (B) Histidine (C) Ornithine (D) Citrulline

Description : An amino acid not involved in urea cycle is (A) Arginine (B) Histidine (C) Ornithine (D) Citrulline

Last Answer : Answer : B

Conversion of ammonia to urea is done by (a) ornithine cycle (b) arginine cycle (c) fumaric cycle (d) citrulline cycle.

Description : Conversion of ammonia to urea is done by (a) ornithine cycle (b) arginine cycle (c) fumaric cycle (d) citrulline cycle.

Last Answer : (a) ornithine cycle

The following enzyme of urea cycle is present in cytosol: (A) Argininosuccinic acid synthetase (B) Argininosuccinase (C) Arginase (D) All of these

Description : The following enzyme of urea cycle is present in cytosol: (A) Argininosuccinic acid synthetase (B) Argininosuccinase (C) Arginase (D) All of these

Last Answer : Answer : D

The acid amide of Aspartic acid is (A) Glutamine (B) Arginine (C) Aspargine (D) Ornithine

Description : The acid amide of Aspartic acid is (A) Glutamine (B) Arginine (C) Aspargine (D) Ornithine

Last Answer : Answer : C

Sakaguchi reaction is answered by (A) Lysine (B) Ornithine (C) Arginine (D) Arginino succinic acid

Description : Sakaguchi reaction is answered by (A) Lysine (B) Ornithine (C) Arginine (D) Arginino succinic acid

Last Answer : Answer : C

The amino acid which contains a guanidine group is (A) Histidine (B) Arginine (C) Citrulline (D) Ornithine

Description : The amino acid which contains a guanidine group is (A) Histidine (B) Arginine (C) Citrulline (D) Ornithine

Last Answer : Answer : B

Urea is produced physiologically by the action of the enzyme: (A) Urease (B) Glutaminase (C) Arginase (D) None of these

Description : Urea is produced physiologically by the action of the enzyme: (A) Urease (B) Glutaminase (C) Arginase (D) None of these

Last Answer : Answer : C

Enzyme involved in joining together two substrates is (A) Glutamine synthetase (B) Aldolase (C) Gunaine deaminase (D) Arginase

Description : Enzyme involved in joining together two substrates is (A) Glutamine synthetase (B) Aldolase (C) Gunaine deaminase (D) Arginase

Last Answer : Answer : A

Arginase enzyme is formed by (a) Spleen (b) Liver (c) Kidney (d) All

Description : Arginase enzyme is formed by (a) Spleen (b) Liver (c) Kidney (d) All

Last Answer : (b) Liver

Enzyme arginase is found in (a) Mouth cavity (b) Stomach (c) Intestine (d) Liver

Description : Enzyme arginase is found in (a) Mouth cavity (b) Stomach (c) Intestine (d) Liver

Last Answer : (d) Liver

Enzyme deficient in Hyperammonemia type II is (A) Glutamine synthetase (B) Glutaminase (C) Ornithine transcarbamoylase (D) Carbamoylphosphate synthetase

Description : Enzyme deficient in Hyperammonemia type II is (A) Glutamine synthetase (B) Glutaminase (C) Ornithine transcarbamoylase (D) Carbamoylphosphate synthetase

Last Answer : Answer : C

An enzyme which is excreted in urine is (A) Lactase dehydrogenase (B) Amylase (C) Ornithine transcarbamoylase (D) None of these

Description : An enzyme which is excreted in urine is (A) Lactase dehydrogenase (B) Amylase (C) Ornithine transcarbamoylase (D) None of these

Last Answer : Answer : C

Transfer of the carbamoyl moiety of carbamoyl phosphate to ornithine is catalysed by a liver mitochondrial enzyme: (A) Carbamoyl phosphate synthetase (B) Ornithine transcarbamoylase (C) N-acetyl glutamate synthetase (D) N-acetyl glutamate hydrolase

Description : Transfer of the carbamoyl moiety of carbamoyl phosphate to ornithine is catalysed by a liver mitochondrial enzyme: (A) Carbamoyl phosphate synthetase (B) Ornithine transcarbamoylase (C) N-acetyl glutamate synthetase (D) N-acetyl glutamate hydrolase

Last Answer : Answer : B

Which of the following enzyme defects is associated with a characteristic body odour? 1) Phenylalanine aminotransferase 2) Galactose0-phosphate-uridyltransferase 3) Ornithine transcarbamylase deficiency 4) Fumaryl acetoacetase 5) Branched chain ketoacid decarboxylase

Description : Which of the following enzyme defects is associated with a characteristic body odour? 1) Phenylalanine aminotransferase 2) Galactose0-phosphate-uridyltransferase 3) Ornithine transcarbamylase deficiency 4) Fumaryl acetoacetase 5) Branched chain ketoacid decarboxylase

Last Answer : Answers-5 The following inborn errors of amino acid metabolism are associated with abnormal odours: Glutaric acidaemia type II (sweaty feet), hawkinsinuria (swimming pool), isovaleric acidaemia (sweaty feet), ... The general rule is that if a child smells peculiar he requires a metabolic work-up.

Which one of the following pair of waste substances is removed from blood in ornithine cycle `:`

Description : Which one of the following pair of waste substances is removed from blood in ornithine cycle `:`

Last Answer : Which one of the following pair of waste substances is removed from blood in ornithine cycle `:` A. ` ... CO_(2)` and ammonia D. Urea and sodium salt

Ornithine cycle performs

Description : Ornithine cycle performs

Last Answer : Ornithine cycle performs A. ATP synthesis B. Urea formation in spleen C. Urea formation in liver D. Urin formation in liver

Ornithine cycle operates in

Description : Ornithine cycle operates in

Last Answer : Ornithine cycle operates in A. Stomach B. Pancreas C. Liver D. Oral cavity

Ornithine cycle is related to

Description : Ornithine cycle is related to

Last Answer : Ornithine cycle is related to A. Respiration B. Excretion C. Digestion D. Nutrition

The metabolite which sustains urea cycle is (A) Ornithine (B) Citrulline (C) Carbamoyl phosphate (D) n-acetyl glutamate

Description : The metabolite which sustains urea cycle is (A) Ornithine (B) Citrulline (C) Carbamoyl phosphate (D) n-acetyl glutamate

Last Answer : Answer : C

The ornithine cycle removes two waste products from the blood in liver. These products are (a) CO2 and ammonia (b) ammonia and uric acid (c) CO2 and urea (d) ammonia and urea.

Description : The ornithine cycle removes two waste products from the blood in liver. These products are (a) CO2 and ammonia (b) ammonia and uric acid (c) CO2 and urea (d) ammonia and urea.

Last Answer : a) CO2 and ammonia

In ureotelic animals, urea is formed by (a) Krebs’ cycle (b) EM pathway (c) Ornithine cycle (d) Cori cycle.

Description : In ureotelic animals, urea is formed by (a) Krebs’ cycle (b) EM pathway (c) Ornithine cycle (d) Cori cycle.

Last Answer : (c) Ornithine cycle

In ornithine cycle, which of the following wastes are removed from the blood? (a) CO2 and urea (b) Ammonia and urea (c) CO2 and ammonia (d) Urea and urine

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Description : What do you call the Enzyme that breaks down dairy sugar?

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Description : What enzyme breaks down lactase?

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Deficiency of urea cycle enzymes results into accumulation of citrulline argininosuccinate arginine in the liver resulting in increasing concentration of …….. in the blood. (A) Calcium (B) Sodium (C) Ammonia (D) Lipid

Description : Deficiency of urea cycle enzymes results into accumulation of citrulline argininosuccinate arginine in the liver resulting in increasing concentration of …….. in the blood. (A) Calcium (B) Sodium (C) Ammonia (D) Lipid

Last Answer : Answer : C

ATP is required in following reactions of urea cycle: (A) Synthesis of carbamoyl phosphate and citrulline (B) Synthesis of citrulline and argininosuccinate (C) Synthesis of argininosuccinate and arginine (D) Synthesis of carbamoyl phosphate and argininosuccinate

Description : ATP is required in following reactions of urea cycle: (A) Synthesis of carbamoyl phosphate and citrulline (B) Synthesis of citrulline and argininosuccinate (C) Synthesis of argininosuccinate and arginine (D) Synthesis of carbamoyl phosphate and argininosuccinate

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