Description : The rate limiting step in catecholamine synthesis is catalysed by (A) Phenylalanine hydroxylase (B) Tyrosine hydroxylase (C) Dopa decarboxylase (D) Phenylethanolamine N-methyl transferase
Last Answer : Answer : B
Description : For Catecholamine biosynthesis the rate limiting enzyme is (A) DOPA decarboxylase (B) DOPAMINE β-hydroxylase (C) Tyrosine hydroxylase (D) Phenylalanine hydroxylase
Last Answer : Answer : C
Description : Immediate precursor of epinephrine is (A) Metanephrine (B) Norepinephrine (C) Dopa (D) Dopamine
Description : In the synthetic pathway of epinephrine, disulfiram (antabuse) inhibits the enzyme: (A) Tyrosine hydroxylase (B) Dopamine β-hydroxylase (C) DOPA decarboxylase (D) N-methyl transferase
Description : Formation of melanin from tyrosine requires the action of (A) Dopa decarboxylation (B) Diamine oxidase (C) Peroxidase (D) Tyrosinase
Last Answer : Answer : D
Description : In mammalian tissues serine can be a biosynthetic precursor of (A) Methionine (B) Glycine (C) Tryptophan (D) Phenylalanine
Description : Tyrosine hydroxylase is inhibited by (A) Catecholamines (B) α−Methyldopa (C) Phenylalanine (D) Vanillyl mandelic acid
Last Answer : Answer : A
Description : Melatonin is synthesised from (A) Phenylalanine (B) Tyrosine (C) Tryptophan (D) None of these
Description : Thyroid hormones are synthesized by the iodination of the amino acid: (A) Glycine (B) Phenylalanine (C) Alanine (D) Tyrosine
Description : A characteristic of pheochromocytoma is elevated urinary excretion of (A) Dopamine (B) Tyrosine (C) Vinylmandelic acid (D) Phenylalanine
Description : Neonatal tyrosinemia is due to deficiency of the enzyme: (A) p-Hydroxyphenylpyruvate hydroxylase (B) Fumarylacetoacetate hydrolase (C) Phenylalanine hydroxylase (D) Tyrosine dehydrogenase
Description : Albinism is due to deficiency of the enzyme: (A) Phenylalanine hydroxylase (B) Tyrosinase (C) p-Hydroxyphenylpyruvic acid oxidase (D) Tyrosine dehydrogenase
Description : Activation or inactivation of certain key regulatory enzymes is accomplished by covalent modification of the amino acid: (A) Tyrosine (B) Phenylalanine (C) Lysine (D) Serine
Description : Niacin can be synthesised in human beings from (A) Histidine (B) Phenylalanine (C) Tyrosine (D) Tryptophan
Description : Richner-Hanhart syndrome is due to defect in (A) Tyrosinase (B) Phenylalanine hydroxylase (C) Hepatic tyrosine transaminase (D) Fumarylacetoacetate hydrolase
Description : Million’s test is positive for (A) Phenylalanine (B) Glycine (C) Tyrosine (D) Proline
Description : Which one of the following is an essential amino acid? (A) Arginine (B) Tyrosine (C) Phenylalanine (D) Proline
Description : Serotonin is synthesised from (A) Serine (B) Phenylalanine (C) Tyrosine (D) Tryptophan
Description : All the following statements about phenylketonuria are correct except (A) Phenylalanine cannot be converted into tyrosine (B) Urinary excretion of phenylpyruvate and phenyllactate is increased (C) It ... diet (D) It leads to decreased synthesis of thyroid hormones, catecholamines and melanin
Description : The limiting amino acid of rice is (A) Lysine (B) Tryptophan (C) Phenylalanine (D) Tyrosine
Description : The rate limiting step in the biosynthesis of catecholamines is (A) Decarboxylation of dihydroxyphenylalanine (B) Hydroxylation of phenylalanine (C) Hydroxylation of tyrosine (D) Oxidation of dopamine
Description : Million-Nasse’s reaction is specific for the amino acid: (A) Tryptophan (B) Tyrosine (C) Phenylalanine (D) Arginine
Description : Following events occur in the cytoplasm and not inside storage vesicles, except (a) Conversion of tyrosine to dopa (b) Conversion of dopa to dopamine (c) Conversion of dopamine to norepinephrine (d) Conversion of dopamine to 3,4 dihydroxy phenyl acetic acid
Last Answer : Ans: C
Description : The rate limiting enzyme in the synthesis of catecholamines is: A. Tyrosine hydroxylase B. Dopa decarboxylase C. Dopamine β-hydroxylase D. Noradrenaline N-methyl transferase
Last Answer : A. Tyrosine hydroxylase
Description : In carcinoid syndrome the argentaffin tissue of the abdominal cavity overproduce (A) Serotonin (B) Histamine (C) Tryptamine (D) Tyrosine
Description : .Khorana first deciphered the triplet codons of (a) serine and isoleucine (b) cysteine and valine (c) tyrosine and tryptophan (d) phenylalanine and methinonine.
Last Answer : (a) serine and isoleucine
Description : Khorana first deciphered the triplet codons of (a) serine and isoleucine (b) cysteine and valine (c) tyrosine and tryptophan (d) phenylalanine and methinonine
Last Answer : (b) cysteine and valine
Last Answer : (D) Tryptophan
Description : Phenylalanine, ornithine and methionine are involved in the biogenesis of (A) Lysergic acid (B) Reserpine (C) L-Hyoscyamine (D) Papaverine
Description : Is taking l-dopa illegal ?
Last Answer : Just to clarify – are you saying that you have not done meth ever but you have taken L-dopa?
Description : L-dopa is a drug to cure which disease?
Last Answer : Parkinson's disease
Description : Dopa decarboxylase is inhibited by (A) Epinephrine (B) Norepinephrine (C) α−Methyldopa (D) None of these
Description : An enzyme involved in catabolism of catecholamines is (A) Dopa decarboxylase (B) Aromatic amino acid decarboxylase (C) Monoamine oxidase (D) Catechol oxidas
Description : Blood brain barrier can be crossed by (A) Epinephrine (B) Dopamine (C) Dopa (D) All of these
Description : Methyl dopa decreases blood pressure by (A) Inhibiting the synthesis of catecholamines (B) Antagonising the action of aldosterone (C) Stimulating the release of renin (D) Inhibiting the breakdown of angiotensin
Description : DOPA is an intermediate in the synthesis of (A) Thyroid hormones (B) Catecholamines (C) Melanin (D) Catecholamines and melanin
Description : Maple syrup urine disease results from absence or serve deficiency of (A) Homogentisate oxidase (B) Phenylalanine hydroxylase (C) Branched chain amino acid transaminase (D) None of these
Description : Gout is a metabolic disorder of catabolism of (A) Pyrimidine (B) Purine (C) Alanine (D) Phenylalanine
Description : In the B chain of insulin molecule, the Nterminal amino acid is (A) Proline (B) Threonine (C) Phenylalanine (D) Lysine
Description : In A chain of the insulin molecule the Nterminal amino acid is (A) Glycine (B) Valine (C) Serine (D) Phenylalanine
Description : From the pentapeptide, phe-ala-leu-lysarg, phenylalanine residue is split off by (A) Trypsin (B) Chymotrypsin (C) Aminopeptidase (D) Carboxypeptidase
Description : Cysteine can partially meet the requirement of (A) Phenylalanine (B) Threonine (C) Methionine (D) None of these
Description : Absence of phenylalanine hydroxylase causes (A) Neonatal tyrosinemia (B) Phenylketonuria (C) Primary hyperoxaluria (D) Albinism
Description : The amino acid which synthesizes many hormornes: (A) Valine (B) Phenylalanine (C) Alanine (D) Histidine
Description : All the following are true about phenylketonuria except (A) Deficiency of phenylalanine hydroxylase (B) Mental retardation (C) Increased urinary excretion of p-hydroxyphenyl pyruvic acid (D) Decrease serotonin formation
Description : All the following amino acids are optically active except (A) Tryptophane (B) Phenylalanine (C) Valine (D) Glycine
Description : The amino acid containing an indole ring: (A) Tryptophan (B) Arginine (C) Threonine (D) Phenylalanine
Description : Seratonin is derived in the body from the following amino acid: (A) Phenylalanine (B) Histidine (C) Tryptophan (D) Serine
Description : Hydroxylation of phenylalanine requires all of the following except (A) Phenylalanine hydroxylase (B) Tetrahydrobiopterin (C) NADH (D) Molecular oxygen