Last 5 Year PYQs in Biochemistry for NEET PG
Jan 30, 2025

Biochemistry is one of the most crucial subjects to conquer in NEET PG. If you can ace the subject, no one can stop you from acing the exam. No matter how overwhelming memorising Biochemistry concepts can be, the prep can be made smoother if you focus on Previous Years’ Questions.
However, for you to do that, you don’t need to peruse various resources and waste your time. We’ve brought for you the list of high-yield PYQs from the last five years. These will help you identify important patterns, reinforce key concepts, and boost your confidence before the exam.
Let’s dive right in and help you ace the exam.
Download FREE PDFs of Last 5-Year NEET PG PYQs – All Subjects
Q1. What is the function of the proteasome?
- Protein folding
- Pot-translation modification
- Protein degradation
- Protein sorting
Ans. 3) Protein degradation
Q2. Replacing alanine by which amino acid, will increase the UV absorbance of protein at 280nm wavelength?
- Leucine
- Proline
- Arginine
- Tryptophan
Ans. 4) Tryptophan
Also read: Last 5 Years PYQs of INI-CET Anesthesia
Q3. Which of the following contains the maximum amount of vitamin B12?
- Animal products
- Green leafy vegetables
- Roots and tubers
- Vegetarian diet
Ans. 1) Animal products
Q4. Which of the following is involved in the synthesis of apolipoprotein B48?
- RNA alternate splicing
- RNA editing
- DNA editing
- RNA interference
Ans. 2) RNA editing
Q5. In a patient with obstructive jaundice, which of the following outcomes may be observed in Van der Bergh's reaction?
- Direct positive
- Indirect positive
- Both positive
- Coproporphyrin
Ans. 1) Direct positive
Also read: Last 5 Years PYQs INI-CET Biochemistry
Q6. A patient presented with symptoms of delayed adaptation to vision in dark places, gritty sensation in the eyes, dry eyes, and softening of the cornea. What is the likely deficiency in this case?
- Retinoic acid
- Riboflavin
- Niacin
- Pantothenic acid
Ans. 4) Pantothenic acid
Q7. You are conducting an experiment on mitochondrial respiration. You add malate/pyruvate and respiration is normal. You add succinate and respiration is normal. When you add another substance in the presence of pyruvate/succinate and malate, respiration is blocked. Which of the following substances is most likely added?
- Rotenone
- Antimycin A
- Oligomycin
- 2,4-dinitrophenol
Ans. 3) Oligomycin
Q8. What could be the possible diagnosis for a patient who exhibited tendon xanthomas, with his lipid profile indicating serum cholesterol levels of 283 mg/dL and serum LDL levels of 202 mg/dL, and subsequently initiated on lovastatin treatment?
- Familial hypercholesterolemia
- Tangier’s disease
- Lipoprotein lipase deficiency
- Familial hyperchylomicronemia
Ans. 1) Familial hypercholesterolemia
Also read: Last 5 Years PYQs of INI CET Dermatology
Q9. Which of the following glycosaminoglycans (GAGs) are responsible for corneal transparency?
- Keratan sulfate
- Chondroitin sulfate
- Heparin sulfate
- Hyaluronic acid
Ans.1) Keratan sulfate
Q10. In this scenario, what is the origin of the blood glucose measured at 7 am the following morning for an individual who had dinner at 8 pm the previous night?
- Hepatic glycogenolysis
- Hepatic gluconeogenesis
- Muscle glycogenolysis
- Dietary glucose
Ans. 1) Hepatic glycogenolysis
Q11. In a patient who hails from a Mediterranean country and travels to Africa, they contract malaria. After receiving treatment with primaquine, the patient subsequently develops hemolytic anemia. Which pathway deficiency in the enzyme could potentially be responsible for this condition?
- Glycolysis
- Gluconeogenesis
- Hexose monophosphate (HMP) pathway
- Luebering-Rapoport pathway
Ans. 3) Hexose monophosphate (HMP) pathway
Also read: Last 5 year PYQs in Psychiatry for NEET PG
Q12. Which of the subsequent disorders exhibits an autosomal recessive inheritance pattern?
- Huntington’s disease
- Treacher collins syndrome
- Cystic fibrosis
- Achondroplasia
Ans. 3) Cystic fibrosis
Q13. Which of the options aids in the transportation of fatty acids through the inner mitochondrial membrane?
- Acyl carrier protein
- Carnitine
- Lecithin-cholesterol acyltransferase
- Albumin
Ans. 2) Carnitine
Q14. What is the term for a single mutation in a nucleotide base pair that leads to the formation of a termination codon?
- Missense mutation
- Nonsense mutation
- Stop mutation
- Silent mutation
Ans. 2) Nonsense mutation
Also read: Last 5 year PYQs in ophthalmology for NEET PG
Q15. Which process is responsible for DNA packaging?
- Histone
- Glycoprotein
- Nucleic acid
- Adenine
Ans. 1) Histone
Q16. Which of the subsequent diseases demonstrate autosomal recessive inheritance?
- Albinism
- G6PD deficiency
- Marfan’s syndrome
- Lesch-Nyhan syndrome
Ans. 1) Albinism
Q17. Which of the following deficiencies leads to an elevation of glutamine levels in the bloodstream?
- Arginosuccinate lyase
- Alpha-galactosidase-A
- Ornithine transcarbamoylase
- Arginase
Ans. 3) Ornithine transcarbamoylase
Also read: Last 5 Years PYQs in Radiology for NEET PG
Q18. Which amino acid is essential for the conversion of nor-epinephrine to epinephrine among the following options?
- Tyrosine
- Tryptophan
- Phenylalanine
- Methionine
Ans. 4) Methionine
Q19. In cerebrohepatorenal syndrome, an infant exhibits symptoms of hypotonia and seizures. The condition is characterized by the accumulation of which substance in the brain?
- Glucose
- Long chain fatty acid
- Lactic acid
- Triglycerides
Ans. 2) Long chain fatty acid
Also read: Last 5 Year PYQs in Pharmacology for NEET PG
Q20. Which substrate of the Krebs cycle is diminished by an excess amount of ammonia?
- Malate
- Oxaloacetate
- Fumarate
- Alpha ketoglutarate
Ans. 4) Alpha ketoglutarate
If you wish to access the detailed explanations for the correct and incorrect options of download the Pdf now.
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