Essential fructosuria is characterized by the lack of the hepatic enzyme: (A) Phosphohexose isomerase (B) Aldalose A (C) Aldolase B (D) Fructokinase

Essential fructosuria is characterized by the lack of the hepatic enzyme: (A) Phosphohexose isomerase (B) Aldalose A (C) Aldolase B (D) Fructokinase
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Hereditary fructose intolerance involves the absence of the enzyme: (A) Aldalose B (B) Fructokinase (C) Triokinase (D) Phosphotriose isomerase

Description : Hereditary fructose intolerance involves the absence of the enzyme: (A) Aldalose B (B) Fructokinase (C) Triokinase (D) Phosphotriose isomerase

Last Answer : Answer : A

Hemolytic anemia is caused by the deficiency of certain enzymes of the pentose phosphate pathway, the principal enzyme involved is (A) Glucose-6-phosphate dehydrogenase (B) Aldolase (C) Fructose 1, 6-bisphosphatase (D) Phosphohexose isomerase

Description : Hemolytic anemia is caused by the deficiency of certain enzymes of the pentose phosphate pathway, the principal enzyme involved is (A) Glucose-6-phosphate dehydrogenase (B) Aldolase (C) Fructose 1, 6-bisphosphatase (D) Phosphohexose isomerase

Last Answer : Answer : A

Which of the following is an allosteric enzyme? (A) Phosphohexose isomerase (B) Phosphotriose isomerase (C) Lactate dehydrogenase (D) Phosphofructokinase

Description : Which of the following is an allosteric enzyme? (A) Phosphohexose isomerase (B) Phosphotriose isomerase (C) Lactate dehydrogenase (D) Phosphofructokinase

Last Answer : Answer : D

An enzyme involved in gluconeogenesis is (A) Pyruvate kinase (B) Pyruvate carboxylase (C) Hexokinase (D) Phosphohexose isomerase

Description : An enzyme involved in gluconeogenesis is (A) Pyruvate kinase (B) Pyruvate carboxylase (C) Hexokinase (D) Phosphohexose isomerase

Last Answer : Answer : B

During glycolysis, Fructose 1, 6 diphosphate is decomposed by the enzyme: (A) Enolase a (B) Fructokinase (C) Aldolase (D) Diphosphofructophosphatose

Description : During glycolysis, Fructose 1, 6 diphosphate is decomposed by the enzyme: (A) Enolase a (B) Fructokinase (C) Aldolase (D) Diphosphofructophosphatose

Last Answer : C

Glucose-6-phosphate is an allosteric inhibitor of (A) Glucokinase (B) Hexokinase (C) Phosphohexose isomerase (D) None of these

Description : Glucose-6-phosphate is an allosteric inhibitor of (A) Glucokinase (B) Hexokinase (C) Phosphohexose isomerase (D) None of these

Last Answer : Answer : B

One of the enzymes regulating glycolysis is (A) Phosphofructokinase (B) Glyceraldehyde-3-phosphate dehydrogenase (C) Phosphotriose isomerase (D) Phosphohexose isomerase

Description : One of the enzymes regulating glycolysis is (A) Phosphofructokinase (B) Glyceraldehyde-3-phosphate dehydrogenase (C) Phosphotriose isomerase (D) Phosphohexose isomerase

Last Answer : Answer : A

The enzyme involved in essential pentosuria is (A) Reductase (B) Hydroxylase (C) Isomerase (D) Racemase

Description : The enzyme involved in essential pentosuria is (A) Reductase (B) Hydroxylase (C) Isomerase (D) Racemase

Last Answer : Answer : A

Albinism is a congenital disorder resulting from the lack of which enzyme? (a) Tyrosinase (b) Xanthine oxidase (c) Catalase (d) Fructokinase

Description : Albinism is a congenital disorder resulting from the lack of which enzyme? (a) Tyrosinase (b) Xanthine oxidase (c) Catalase (d) Fructokinase

Last Answer : (a) Tyrosinase

Insulin has no effect on the activity of the enzyme: (A) Glycogen synthetase (B) Fructokinase (C) Pyruvate kinase (D) Pyruvate dehydrogenase

Description : Insulin has no effect on the activity of the enzyme: (A) Glycogen synthetase (B) Fructokinase (C) Pyruvate kinase (D) Pyruvate dehydrogenase

Last Answer : Answer : B

Conversion of fructose to sorbitol is catalysed by the enzyme: (A) Sorbitol dehydrogenase (B) Aldose reductase (C) Fructokinase (D) Hexokinase

Description : Conversion of fructose to sorbitol is catalysed by the enzyme: (A) Sorbitol dehydrogenase (B) Aldose reductase (C) Fructokinase (D) Hexokinase

Last Answer : Answer : A

Zinc is a constituent of the enzyme: (A) Succinate dehydrogenase (B) Carbonic anhydrase (C) Mitochondrial superoxide dismutase (D) Aldolase

Description : Zinc is a constituent of the enzyme: (A) Succinate dehydrogenase (B) Carbonic anhydrase (C) Mitochondrial superoxide dismutase (D) Aldolase

Last Answer : Answer : B

A mitochondrial marker enzyme is (A) Aldolase (B) Amylase (C) Succinic dehydrogenase (D) Pyruvate dehydrogenase ENZYMES 175

Description : A mitochondrial marker enzyme is (A) Aldolase (B) Amylase (C) Succinic dehydrogenase (D) Pyruvate dehydrogenase ENZYMES 175

Last Answer : Answer : C

A substrate for the enzyme aldolase is (A) galactose-6-phosphate (B) isocitric acid (C) Glucose-1-phosphate (D) Fructose 1, 6 diphosphate

Description : A substrate for the enzyme aldolase is (A) galactose-6-phosphate (B) isocitric acid (C) Glucose-1-phosphate (D) Fructose 1, 6 diphosphate

Last Answer : Answer : D

The enzyme of the glycolic pathway, sensitive to inhibiton by fluoride ions is (A) Hexokinase (B) Aldolase (C) Enolase (D) Pyruvate kinase

Description : The enzyme of the glycolic pathway, sensitive to inhibiton by fluoride ions is (A) Hexokinase (B) Aldolase (C) Enolase (D) Pyruvate kinase

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

The following enzyme is required for the hexose monophosphate shunt pathway: (A) Glucose-6-phosphatase (B) Phosphorylase (C) Aldolase (D) Glucose-6-phosphate dehydrogenase

Description : The following enzyme is required for the hexose monophosphate shunt pathway: (A) Glucose-6-phosphatase (B) Phosphorylase (C) Aldolase (D) Glucose-6-phosphate dehydrogenase

Last Answer : D

Menke’s disease (Kinky or steel hair disease) is a X-linked disease characterized by (A) High levels of plasma copper (B) High levels of ceruloplasmin (C) Low levels of plasma copper and of ceuloplasmin (D) High level of hepatic copper

Description : Menke’s disease (Kinky or steel hair disease) is a X-linked disease characterized by (A) High levels of plasma copper (B) High levels of ceruloplasmin (C) Low levels of plasma copper and of ceuloplasmin (D) High level of hepatic copper

Last Answer : Answer : C

Conversion of testosterone to estradiol requires the enzyme: (A) Aromatase (B) Dehydrogenase (C) Lyase (D) Isomerase HORMONE METABOLISM 215

Description : Conversion of testosterone to estradiol requires the enzyme: (A) Aromatase (B) Dehydrogenase (C) Lyase (D) Isomerase HORMONE METABOLISM 215

Last Answer : Answer : A

The enzyme catalyzing conversion of androstenedione to testosterone is a (A) Oxygenase (B) Dehydrogenase (C) Isomerase (D) Decarboxylase

Description : The enzyme catalyzing conversion of androstenedione to testosterone is a (A) Oxygenase (B) Dehydrogenase (C) Isomerase (D) Decarboxylase

Last Answer : Answer : B

In biosynthesis of cholesterol triparanol inhibits the activity of the enzyme: (A) ∆24 Reductase (B) Oxidosqualene-lanosterol cyclase (C) Isomerase (D) Squalene epoxidase ENZYMES 155

Description : In biosynthesis of cholesterol triparanol inhibits the activity of the enzyme: (A) ∆24 Reductase (B) Oxidosqualene-lanosterol cyclase (C) Isomerase (D) Squalene epoxidase ENZYMES 155

Last Answer : Answer : A

In glycolytic pathway, iodacetate inhibits the activity of the enzyme: (A) Phosphotriose isomerase (B) Glyceraldehyde-3-phosphate dehydrogenase (C) Pyruvate kinase (D) Phosphofructokinase

Description : In glycolytic pathway, iodacetate inhibits the activity of the enzyme: (A) Phosphotriose isomerase (B) Glyceraldehyde-3-phosphate dehydrogenase (C) Pyruvate kinase (D) Phosphofructokinase

Last Answer : Answer : B

Alkaptonuria occurs due to deficiency of the enzyme: (A) Maleylacetoacetate isomerase (B) Homogentisate oxidase (C) p-Hydroxyphenylpyruvate hydroxylase (D) Fumarylacetoacetate hydrolase

Description : Alkaptonuria occurs due to deficiency of the enzyme: (A) Maleylacetoacetate isomerase (B) Homogentisate oxidase (C) p-Hydroxyphenylpyruvate hydroxylase (D) Fumarylacetoacetate hydrolase

Last Answer : Answer : B

What is fructosuria?

Description : What is fructosuria?

Last Answer : It is a benign metabolic defect due to deficiency of fructokinase. Urine gives positive Benedictís test, and so it should be differentiated from diabetes mellitus.

What is fructosuria?

Description : What is fructosuria?

Last Answer : Presence of fructose in urine. It is due to the deficiency of fructokinase or aldolase B 

The other name of invertase enzyme is A- sucrose B- saccharase C- isomerase D- both (a) and (b

Description : The other name of invertase enzyme is A- sucrose B- saccharase C- isomerase D- both (a) and (b

Last Answer : both (a) and (b)

Fructose 2, 3 bi phosphate is a powerful allosteric activator of (A) Fructose 1, 6 diphosphatase (B) Phosphofructokinase (C) Hexokinase (D) Fructokinase

Description : Fructose 2, 3 bi phosphate is a powerful allosteric activator of (A) Fructose 1, 6 diphosphatase (B) Phosphofructokinase (C) Hexokinase (D) Fructokinase

Last Answer : Answer : B

A specific fructokinase present in liver has a very high affinity for its substrate because (A) Km for fructose is very high (B) Km for fructose is very low (C) Activity is affected by fasting (D) Activity is affected by insulin

Description : A specific fructokinase present in liver has a very high affinity for its substrate because (A) Km for fructose is very high (B) Km for fructose is very low (C) Activity is affected by fasting (D) Activity is affected by insulin

Last Answer : Answer : B

Hexokinase has a high affinity for glucose than (A) Fructokinase (B) Galactokinase (C) Glucokinase (D) All of the above

Description : Hexokinase has a high affinity for glucose than (A) Fructokinase (B) Galactokinase (C) Glucokinase (D) All of the above

Last Answer : C

Glycogen synthetase activity is depressed by (A) Glucose (B) Insulin (C) Cyclic AMP (D) Fructokinase

Description : Glycogen synthetase activity is depressed by (A) Glucose (B) Insulin (C) Cyclic AMP (D) Fructokinase

Last Answer : C

Fructokinase catalyses which reaction?

Description : Fructokinase catalyses which reaction?

Last Answer : Fructose to fructose-1-phosphate. 

What is the importance of phospho fructokinase?

Description : What is the importance of phospho fructokinase?

Last Answer : It is the key enzyme (rate limiting enzyme) of the pathway. It is an irreversible reaction. 

An example of ligases is (A) Succinate thiokinase (B) Alanine racemase (C) Fumarase (D) Aldolase

Description : An example of ligases is (A) Succinate thiokinase (B) Alanine racemase (C) Fumarase (D) Aldolase

Last Answer : Answer : A

Which of the following is a substrate for aldolase activity in Glycolytic pathway? (A) Glyceraldehyde-3-p (B) Glucose-6-p (C) Fructose-6-p (D) Fructose1, 6-bisphosphate

Description : Which of the following is a substrate for aldolase activity in Glycolytic pathway? (A) Glyceraldehyde-3-p (B) Glucose-6-p (C) Fructose-6-p (D) Fructose1, 6-bisphosphate

Last Answer : D

What is the substrate for aldolase reaction?

Description : What is the substrate for aldolase reaction?

Last Answer : Fructose-1,6-bisphosphate.

What are the symptoms of fructosuria?

Description : What are the symptoms of fructosuria?

Last Answer : Hello, symptoms will vary based on the origin of the disease. If you were born with the condition, symptoms include: a strong dislike of sweets, growth delays, vomiting, jaundice, impaired physical development ... , your symptoms are gas, nausea, vomiting, and bloating. I hope this helps! -Diana

Tarui disease is characterized by the deficiency of the enzyme: (A) Liver phosphorylase (B) Muscle phosphorylase (C) Muscle and erythrocyte phosphofructokinase (D) Lysosomal acid maltase

Description : Tarui disease is characterized by the deficiency of the enzyme: (A) Liver phosphorylase (B) Muscle phosphorylase (C) Muscle and erythrocyte phosphofructokinase (D) Lysosomal acid maltase

Last Answer : Answer : C

Her’s disease is characterized by deficiency of (A) Muscle phosphorylase (B) Liver phosphorylase (C) Debranching enzyme (D) Glycogen synthase

Description : Her’s disease is characterized by deficiency of (A) Muscle phosphorylase (B) Liver phosphorylase (C) Debranching enzyme (D) Glycogen synthase

Last Answer : Answer : B

Mc Ardle’s syndrome is characterized by the absence of (A) Liver phosphorylase (B) Muscle phosphorylase (C) Branching enzyme (D) Debranching enzyme

Description : Mc Ardle’s syndrome is characterized by the absence of (A) Liver phosphorylase (B) Muscle phosphorylase (C) Branching enzyme (D) Debranching enzyme

Last Answer : Answer : B

Altering the amino acid profile in total parenteral nutrition solutions can be of benefit in certain conditions. Which of the following conditions are associated with a benefit by supplementation with the amino acid type listed? a. Acute renal failure and essential amino acids b. Hepatic failure and aromatic amino acids c. Short gut syndrome and glutamine d. Chronic renal failure and essential amino acids

Description : Altering the amino acid profile in total parenteral nutrition solutions can be of benefit in certain conditions. Which of the following conditions are associated with a benefit by supplementation with the ... c. Short gut syndrome and glutamine d. Chronic renal failure and essential amino acids

Last Answer : Answer: a, c In a number of conditions, altering the amino acid profile of the total parenteral nutrition solution can be of benefit. TPN with amino acids of high biologic value ... Glutamine-enriched TPN partially attenuates villous atrophy and may be useful in treatment of short gut syndrome

3-β-Hydroxysteroid dehydrogenase and ∆5,4 isomerase catalyse the conversion of the weak androgen DHEA to (A) Androstenedione (B) Testosterone (C) Progesterone (D) Estrone

Description : 3-β-Hydroxysteroid dehydrogenase and ∆5,4 isomerase catalyse the conversion of the weak androgen DHEA to (A) Androstenedione (B) Testosterone (C) Progesterone (D) Estrone

Last Answer : Answer : A

In the biosynthesis of cortiol, the sequence of enzymes involved is (A) Hydroxylase–dehydrogenase + isomerase – hydroxylase (B) Dehydrogenase–hydroxylase–isomerase (C) Hydroxylase–lyase–dehydrogenase isomerase (D) Isomerase–lyase–hydroxylase–dehydrogenase

Description : In the biosynthesis of cortiol, the sequence of enzymes involved is (A) Hydroxylase–dehydrogenase + isomerase – hydroxylase (B) Dehydrogenase–hydroxylase–isomerase (C) Hydroxylase–lyase–dehydrogenase isomerase (D) Isomerase–lyase–hydroxylase–dehydrogenase

Last Answer : Answer : A

Urease is a (A) Lyase (B) Ligase (C) Isomerase (D) Hydrolase

Description : Urease is a (A) Lyase (B) Ligase (C) Isomerase (D) Hydrolase

Last Answer : Answer : D

Pyruvate dehydrogenase is a/an (A) Isomerase (B) Lyase (C) Ligase (D) Oxido reductase

Description : Pyruvate dehydrogenase is a/an (A) Isomerase (B) Lyase (C) Ligase (D) Oxido reductase

Last Answer : Answer : D

Two molecules of acetyl-CoA condense to form acetoacetyl-CoA catalysed by (A) Thiolase (B) Kinase (C) Reductase (D) Isomerase

Description : Two molecules of acetyl-CoA condense to form acetoacetyl-CoA catalysed by (A) Thiolase (B) Kinase (C) Reductase (D) Isomerase

Last Answer : Answer : A

From arachidonate, synthesis of prostaglandins is catalysed by (A) Cyclooxygenase (B) Lipoxygenase (C) Thromboxane synthase (D) Isomerase

Description : From arachidonate, synthesis of prostaglandins is catalysed by (A) Cyclooxygenase (B) Lipoxygenase (C) Thromboxane synthase (D) Isomerase

Last Answer : Answer : A

Retinol isomerase is present in (A) Retina (B) Liver (C) Both (A) and (B) (D) None of these

Description : Retinol isomerase is present in (A) Retina (B) Liver (C) Both (A) and (B) (D) None of these

Last Answer : Answer : B

Folding of newly synthesized proteins is accelerated by (A) Protein disulphide isomerase (B) Prolyl cis-trans isomerase (C) Chaperonins (D) All of these

Description : Folding of newly synthesized proteins is accelerated by (A) Protein disulphide isomerase (B) Prolyl cis-trans isomerase (C) Chaperonins (D) All of these

Last Answer : Answer : D

ATP is ‘wasted’ in Rapoport-Lueberring cycle in RBCs as otherwise it will inhibit (A) Phosphoglucomutase (B) Phosphohexo isomerase (C) Phosphofructo kinase (D) Phosphoenol pyruvate carboxy kinase

Description : ATP is ‘wasted’ in Rapoport-Lueberring cycle in RBCs as otherwise it will inhibit (A) Phosphoglucomutase (B) Phosphohexo isomerase (C) Phosphofructo kinase (D) Phosphoenol pyruvate carboxy kinase

Last Answer : C