All Free Biochemistry MCQs with Answers
Every Biochemistry question in the bank, across all chapters, each with the correct answer and a written explanation. Free and unlimited, with no account needed.
393 questions · page 11 of 20
- A. Acetone
- B. Acetocetate
- C. Acetic acid
- D. Beta hydroxybutyric acid
Explanation: The three ketone bodies are acetoacetate, beta-hydroxybutyrate and acetone.
Correct answer: Acetic acid- A. Blood
- B. Kidney
- C. Spleen
- D. Liver
Explanation: Ketone-body formation, or ketogenesis, occurs mainly in the mitochondria of liver cells during fasting or carbohydrate deficiency.
Correct answer: Liver- A. Mitochondria
- B. Microsomes
- C. Cytoplasm
- D. All of the above
Explanation: The principal site of fatty-acid beta-oxidation is the mitochondrial matrix, where fatty acyl-CoA is repeatedly shortened to acetyl-CoA.
Correct answer: Mitochondria- A. Glutamate
- B. Acetoacetate
- C. Cholesterol
- D. Glycine
Explanation: When fatty acid oxidation is high, liver acetyl-CoA accumulates and is diverted into ketogenesis, producing acetoacetate.
Correct answer: Acetoacetate- A. Double unpaired electron in an outer orbit
- B. Single paired electron in an outer orbit
- C. Single unpaired electron in an outer orbit
- D. Double paired electron in an outer orbit
Explanation: A free radical contains at least one unpaired electron, commonly in its outer orbital, making it highly reactive.
Correct answer: Single unpaired electron in an outer orbit- A. Cyclic GMP
- B. Calcium ions
- C. Cyclic AMP
- D. Prostacyclins
Explanation: Nitric oxide activates soluble guanylyl cyclase, increasing cyclic GMP, which mediates effects such as vascular smooth-muscle relaxation.
Correct answer: Cyclic GMP- A. Hypoxia stimulates pyruvate dehydrogenase by increased, 2, 3DPG
- B. Hypoxia stimulates release of all glycolytic enzymes from Band 3 on RBC membrane
- C. Hypoxia inhibits hexokinase
- D. Activation of the regulatory enzymes by high PH
Explanation: During hypoxia, deoxyhaemoglobin binds the cytoplasmic domain of band 3 and displaces glycolytic enzymes, increasing their access to the…
Correct answer: Hypoxia stimulates release of all glycolytic enzymes from Band 3 on RBC membrane- A. Catalase
- B. Acetaldehyde dehydrogenase
- C. Alcohol dehydrogenase
- D. Enolase
Explanation: Alcohol dehydrogenase oxidises ethanol to acetaldehyde, using NAD+ as the electron acceptor.
Correct answer: Alcohol dehydrogenase- A. Creatinine
- B. Phosphates
- C. Xanthine
- D. Uric acid
Explanation: In humans, purine bases are degraded through hypoxanthine and xanthine to uric acid, the principal end product excreted in urine.
Correct answer: Uric acid- A. Urea
- B. Glutamine
- C. Creatinine
- D. Uric Acid
Explanation: Brain tissue detoxifies ammonia by combining it with glutamate to form glutamine through glutamine synthetase.
Correct answer: Glutamine- A. 1 Kcal
- B. 41 Kcal
- C. 410 Kcal
- D. 4100 Kcal
Explanation: Protein yields approximately 4.1 kcal per gram when metabolised, so 10 g provides about 41 kcal.
Correct answer: 41 Kcal- A. Tyrosine transaminase
- B. Cystathionase
- C. Pheylalanine hydroxylase
- D. Homogentisate oxidase
Explanation: Alkaptonuria results from deficiency of homogentisate oxidase in tyrosine degradation, causing homogentisic acid to accumulate and darken…
Correct answer: Homogentisate oxidase- A. Carbamyl synthetase
- B. Urease
- C. Arginase
- D. Ornithine
Explanation: Carbamoyl phosphate synthetase I catalyses the first, committed step of the urea cycle in liver mitochondria, forming carbamoyl phosphate…
Correct answer: Carbamyl synthetase- A. Uric acid
- B. Glutamine
- C. Urea
- D. Creatinine
Explanation: In the liver, toxic ammonia is converted into relatively harmless urea through the urea cycle, allowing its excretion by the kidneys.
Correct answer: Urea- A. Glucose
- B. Fatty acid
- C. Glycerol
- D. Beta hydroxy butyrate
Explanation: After prolonged starvation, the brain adapts to use ketone bodies, especially beta-hydroxybutyrate, reducing its dependence on glucose.
Correct answer: Beta hydroxy butyrate- A. 6alactosemia
- B. Alkaptonuria
- C. Homocystinuria
- D. Phenyl ketonuria
Explanation: Phenylketonuria, alkaptonuria, and homocystinuria result from inherited defects in amino-acid metabolism.
Correct answer: 6alactosemia- A. It is a tripetide
- B. It converts hemoglobin to methemoglobin
- C. It conjugates xenobiotics
- D. It scavenges free radicals and superoxide ions
Explanation: Glutathione is a tripeptide that detoxifies xenobiotics and protects cells by reducing reactive oxygen species.
Correct answer: It converts hemoglobin to methemoglobin- A. Brain
- B. Kidney
- C. Liver
- D. Intestine
Explanation: Urea is formed mainly in the liver through the urea cycle, which converts toxic ammonia into a less toxic compound for renal excretion.
Correct answer: Liver- A. Urease
- B. Uricase
- C. Glutaminase
- D. Arginase
Explanation: Arginase catalyses the final urea-cycle reaction, splitting arginine into urea and ornithine.
Correct answer: Arginase- A. Fumarate
- B. Succinate
- C. Ornithine
- D. Aspartate
Explanation: Argininosuccinate is cleaved in the urea cycle to produce arginine and fumarate.
Correct answer: Fumarate