Biochemistry Notes One Shot

Biochemistry Notes One Shot

Biochemistry Notes One Shot, Biochemistry One Shot

Biochemistry Notes One Shot

Are you preparing for GPAT, NIPER, Pharmacist, Drug Inspector, or NPLEX exams? Our latest blog post provides an extensive set of Biochemistry Notes One Shot & MCQs designed to help you excel in these competitive exams. This quiz-based content is tailored to cover essential biochemical concepts that frequently appear in pharma-related tests.

In this post, you will find high-yield Notes & MCQs on key topics such as:

  • Enzyme active sites and catalytic mechanisms
  • Urea cycle disorders and their clinical significance
  • Vitamins, coenzymes, and related deficiency disorders
  • Metalloenzymes and their biochemical roles
  • Competitive and non-competitive inhibition mechanisms
  • ATP production pathways, glycolysis, and mitochondrial functions

Each question is framed to reflect the exam pattern, enhancing your conceptual clarity and recall ability. Whether you are revising metabolic pathways, enzyme functions, or disorders related to essential vitamins, this blog offers targeted preparation for pharmacy entrance and professional exams.

Features of the Blog:

  • 50+ MCQs with answers and explanations
  • Ideal for GPAT, NIPER, Drug Inspector, and Pharmacist exams
  • Covers essential topics in clinical biochemistry and pharmacology
  • Designed to boost both accuracy and speed

Prepare effectively with these MCQs to secure your success in competitive exams. Start practicing now and elevate your exam readiness with our comprehensive biochemistry quiz!

Biochemistry One Shot


1. Active Centers of Enzymes

  • Chymotrypsin, Trypsin, Thrombin: Histidine (57), Aspartate (102), Serine (195) at the active site.
  • Phosphoglucomutase, Alkaline phosphatase, Acetylcholinesterase: Serine and Histidine are key.
  • Other examples: Carbonic anhydrase, Hexokinase, Carboxypeptidase, Aldolase—feature serine, histidine, or cysteine residues at their catalytic sites.

2. Urea Cycle Disorders

  • Hyperammonemia Type-I: Deficiency in Carbamoyl Phosphate Synthetase I (CPS-I).
  • Hyperammonemia Type-II: Ornithine transcarbamoylase (OTC) deficiency; increased glutamine levels in blood, CSF, and urine.
  • Hyperornithinemia: Defective ornithine transporter protein.
  • Citrullinemia: Caused by a deficiency in argininosuccinate synthetase.
  • Argininosuccinic aciduria: Due to argininosuccinate lyase deficiency.
  • Hyperargininemia: Results from an arginase deficiency, leading to increased arginine levels in blood and CSF.

3. Metabolic Functions of Subcellular Organelles

  • Nucleus: DNA replication, transcription.
  • Endoplasmic Reticulum: Protein synthesis, drug metabolism, cholesterol synthesis.
  • Golgi Body: Protein maturation.
  • Lysosome: Degradation of biomolecules (proteins, carbohydrates, lipids).
  • Mitochondria: Electron transport chain, TCA cycle, beta-oxidation, ketone synthesis, partial urea synthesis.
  • Cytosol: Glycolysis, HMP shunt, fatty acid synthesis, purine/pyrimidine synthesis, protein synthesis.

4. Metalloenzymes and their Associated Metals

  • Zinc: Carbonic anhydrase, alcohol dehydrogenase.
  • Magnesium: Hexokinase, phosphofructokinase.
  • Manganese: Enolase.
  • Copper: Tyrosinase, cytochrome oxidase.
  • Iron: Catalase, peroxidase.
  • Calcium: Lecithinase.
  • Molybdenum: Xanthine oxidase.

5. Fat-Soluble Vitamins and Related Disorders

  • Vitamin A: Deficiency causes night blindness, xerophthalmia, and keratomalacia.
  • Vitamin D: Deficiency leads to rickets in children, osteomalacia in adults.
  • Vitamin E: Antioxidant; deficiency affects fertility (ovum, sperm) and can lead to hemolysis.
  • Vitamin K: Involved in coagulation; deficiency results in bleeding disorders.

6. Essential and Non-Essential Amino Acids

  • Essential: Arginine, Histidine, Isoleucine, Leucine, Lysine, Methionine, Threonine, Valine.
  • Non-Essential: Glycine, Alanine, Serine, Cysteine, Aspartate, Glutamate, Proline.

7. ATP Yield in Glycolysis under Anaerobic Conditions

  • Hexokinase step: -1 ATP.
  • Phosphofructokinase step: -1 ATP.
  • Biphosphoglycerate kinase step: +2 ATP.
  • Pyruvate kinase step: +2 ATP.
  • Net ATP gain per glucose molecule: 2 ATP.

8. Clinically Useful Competitive Inhibitors

  • Allopurinol: Inhibits xanthine oxidase.
  • Dicoumarol: Inhibits Vitamin K epoxide reductase.
  • Penicillin: Targets transpeptidase.
  • Sulfonamides: Inhibit folate synthesis.
  • Trimethoprim & Pyrimethamine: Inhibit dihydrofolate reductase (FH2-reductase).
  • Methotrexate: Inhibits FH2-reductase.
  • 5-Fluorouracil: Targets thymidylate synthase.
  • Lovastatin: Inhibits HMG-CoA reductase (cholesterol synthesis).
  • Oseltamivir (Tamiflu): Inhibits neuraminidase.

9. Comparison of Competitive vs. Non-Competitive Inhibition

FeatureCompetitive InhibitionNon-Competitive Inhibition
Acting siteActive siteAllosteric site
Substrate AnalogYesNo
ReversibilityReversibleOften irreversible
Effect of excess substrateInhibition relievedNo effect
Km (Michaelis constant)IncreasedNo change
Vmax (Maximum velocity)No changeDecreased
SignificanceDrug actionToxicological

10. Coenzymes and the Groups Transferred

  • Thiamine Pyrophosphate (TPP): Transfers hydroxyethyl groups.
  • Pyridoxal Phosphate (PLP): Transfers amino groups.
  • Biotin: Transfers carbon dioxide.
  • Coenzyme-A (CoA): Transfers acyl groups.
  • Tetrahydrofolate (FH4): Transfers one-carbon units.
  • ATP: Transfers phosphate groups.

These notes summarize key biochemical concepts, including enzyme functions, metabolic pathways, vitamins, and clinical applications, providing a concise yet comprehensive overview.

MCQs for Biochemistry

  1. Which amino acid is commonly present at the catalytic site of chymotrypsin?
    a) Glutamate
    b) Serine
    c) Lysine
    d) Alanine
    Answer: b) Serine
  2. Which enzyme deficiency is responsible for Hyperammonemia Type-I?
    a) Ornithine transcarbamoylase (OTC)
    b) Arginase
    c) Carbamoyl Phosphate Synthetase I (CPS-I)
    d) Argininosuccinate synthetase
    Answer: c) Carbamoyl Phosphate Synthetase I (CPS-I)
  3. Which organelle is responsible for ATP production through the electron transport chain?
    a) Golgi body
    b) Mitochondria
    c) Lysosome
    d) Nucleus
    Answer: b) Mitochondria
  4. Which metal ion is present in carbonic anhydrase?
    a) Copper
    b) Iron
    c) Zinc
    d) Magnesium
    Answer: c) Zinc
  5. Deficiency of Vitamin A causes which of the following conditions?
    a) Scurvy
    b) Night blindness
    c) Beriberi
    d) Pellagra
    Answer: b) Night blindness
  6. What is the total net ATP gain per glucose molecule in anaerobic glycolysis?
    a) 4 ATP
    b) 2 ATP
    c) 6 ATP
    d) 1 ATP
    Answer: b) 2 ATP
  7. Which of the following is a competitive inhibitor of xanthine oxidase?
    a) Allopurinol
    b) Dicoumarol
    c) Methotrexate
    d) Penicillin
    Answer: a) Allopurinol
  8. In non-competitive inhibition, the Vmax of the enzyme reaction is:
    a) Increased
    b) Decreased
    c) Unchanged
    d) Doubled
    Answer: b) Decreased
  9. Which of the following vitamins is involved in blood coagulation?
    a) Vitamin A
    b) Vitamin D
    c) Vitamin K
    d) Vitamin E
    Answer: c) Vitamin K
  10. Which amino acid is non-essential?
    a) Leucine
    b) Valine
    c) Glycine
    d) Histidine
    Answer: c) Glycine
  11. Which enzyme is inhibited by Lovastatin?
    a) HMG-CoA reductase
    b) Neuraminidase
    c) Thymidylate synthase
    d) Dihydrofolate reductase
    Answer: a) HMG-CoA reductase
  12. Which coenzyme is involved in the transfer of acyl groups?
    a) Biotin
    b) Coenzyme-A (CoA)
    c) Thiamine Pyrophosphate (TPP)
    d) Pyridoxal Phosphate (PLP)
    Answer: b) Coenzyme-A (CoA)
  13. Which of the following disorders is caused by a deficiency of arginase?
    a) Citrullinemia
    b) Argininosuccinic aciduria
    c) Hyperammonemia Type-II
    d) Hyperargininemia
    Answer: d) Hyperargininemia
  14. In competitive inhibition, which parameter is increased?
    a) Vmax
    b) Km
    c) Enzyme concentration
    d) Substrate concentration
    Answer: b) Km
  15. Which metabolic function is performed by the cytosol?
    a) TCA cycle
    b) Glycolysis
    c) Electron transport chain
    d) Beta-oxidation of fatty acids
    Answer: b) Glycolysis
  1. Which vitamin is an antioxidant and is essential for maintaining healthy sperm motility?
    a) Vitamin A
    b) Vitamin D
    c) Vitamin E
    d) Vitamin K
    Answer: c) Vitamin E
  2. Which enzyme requires biotin as a coenzyme for the transfer of carbon dioxide?
    a) Hexokinase
    b) Acetyl-CoA carboxylase
    c) Phosphoglucomutase
    d) Alcohol dehydrogenase
    Answer: b) Acetyl-CoA carboxylase
  3. Which of the following urea cycle disorders involves defective ornithine transport?
    a) Citrullinemia
    b) Hyperornithinemia
    c) Hyperammonemia Type-I
    d) Argininosuccinic aciduria
    Answer: b) Hyperornithinemia
  4. Which enzyme contains copper and is responsible for melanin synthesis?
    a) Alcohol dehydrogenase
    b) Hexokinase
    c) Tyrosinase
    d) Xanthine oxidase
    Answer: c) Tyrosinase
  5. Which coenzyme transfers phosphate groups during biochemical reactions?
    a) Thiamine Pyrophosphate (TPP)
    b) Tetrahydrofolate (FH4)
    c) Coenzyme-A (CoA)
    d) Adenosine Triphosphate (ATP)
    Answer: d) Adenosine Triphosphate (ATP)
  6. Which of the following is the key function of the lysosome?
    a) Electron transport
    b) Protein maturation
    c) Degradation of cellular waste
    d) Protein synthesis
    Answer: c) Degradation of cellular waste
  7. Which competitive inhibitor targets thymidylate synthase?
    a) 5-Fluorouracil
    b) Allopurinol
    c) Methotrexate
    d) Lovastatin
    Answer: a) 5-Fluorouracil
  8. What is the biochemical significance of the mitochondrial electron transport chain?
    a) Glycolysis
    b) ATP generation
    c) Fatty acid synthesis
    d) Urea synthesis
    Answer: b) ATP generation
  9. Which amino acid is classified as essential?
    a) Glycine
    b) Alanine
    c) Leucine
    d) Glutamate
    Answer: c) Leucine
  10. In competitive inhibition, which factor can relieve inhibition?
    a) Increase in enzyme concentration
    b) Increase in substrate concentration
    c) Decrease in Km
    d) Increase in product concentration
    Answer: b) Increase in substrate concentration
  11. Which enzyme is involved in cholesterol synthesis and is inhibited by statins?
    a) HMG-CoA reductase
    b) Pyruvate kinase
    c) Carbonic anhydrase
    d) Xanthine oxidase
    Answer: a) HMG-CoA reductase
  12. What is the main product of heme degradation in the liver?
    a) Biliverdin
    b) Urobilin
    c) Bilirubin
    d) Stercobilin
    Answer: c) Bilirubin
  13. Which organelle participates in urea synthesis and gluconeogenesis?
    a) Cytosol
    b) Lysosome
    c) Golgi body
    d) Mitochondria
    Answer: d) Mitochondria
  14. Which of the following disorders is inherited in an autosomal recessive manner and involves high levels of citrulline?
    a) Hyperammonemia Type-I
    b) Hyperammonemia Type-II
    c) Citrullinemia
    d) Hyperargininemia
    Answer: c) Citrullinemia
  15. Which vitamin deficiency can result in bleeding disorders and impaired clotting?
    a) Vitamin A
    b) Vitamin D
    c) Vitamin E
    d) Vitamin K
    Answer: d) Vitamin K
  1. Which amino acid is present at the active site of carbonic anhydrase?
    a) Serine
    b) Histidine
    c) Aspartate
    d) Lysine
    Answer: b) Histidine
  2. Which of the following vitamins regulates calcium levels in the body?
    a) Vitamin A
    b) Vitamin D
    c) Vitamin E
    d) Vitamin K
    Answer: b) Vitamin D
  3. Which enzyme is responsible for the final step in glycolysis?
    a) Hexokinase
    b) Pyruvate kinase
    c) Phosphofructokinase
    d) Glucose-6-phosphatase
    Answer: b) Pyruvate kinase
  4. In urea cycle disorders, increased levels of ammonia and citrulline are characteristic of:
    a) Argininosuccinic aciduria
    b) Hyperornithinemia
    c) Hyperammonemia Type-I
    d) Citrullinemia
    Answer: d) Citrullinemia
  5. Which enzyme contains magnesium as a cofactor?
    a) Hexokinase
    b) Tyrosinase
    c) Xanthine oxidase
    d) Lecithinase
    Answer: a) Hexokinase
  6. Which coenzyme is essential for the transfer of amino groups?
    a) Pyridoxal Phosphate (PLP)
    b) Thiamine Pyrophosphate (TPP)
    c) Biotin
    d) Coenzyme-A (CoA)
    Answer: a) Pyridoxal Phosphate (PLP)
  7. What is the primary function of the Golgi apparatus?
    a) ATP generation
    b) Protein maturation
    c) Degradation of lipids
    d) DNA replication
    Answer: b) Protein maturation
  8. Which type of inhibition is generally irreversible?
    a) Competitive inhibition
    b) Non-competitive inhibition
    c) Feedback inhibition
    d) Uncompetitive inhibition
    Answer: b) Non-competitive inhibition
  9. Which urea cycle disorder involves the accumulation of argininosuccinate in blood and urine?
    a) Hyperammonemia Type-I
    b) Argininosuccinic aciduria
    c) Citrullinemia
    d) Hyperornithinemia
    Answer: b) Argininosuccinic aciduria
  10. Which vitamin deficiency is associated with rickets in children?
    a) Vitamin A
    b) Vitamin D
    c) Vitamin E
    d) Vitamin K
    Answer: b) Vitamin D
  11. Which enzyme inhibitor is used to block folate synthesis in bacteria?
    a) Sulfonamides
    b) Allopurinol
    c) Dicoumarol
    d) Lovastatin
    Answer: a) Sulfonamides
  12. Which of the following enzymes is inhibited by methotrexate?
    a) Xanthine oxidase
    b) Dihydrofolate reductase
    c) Thymidylate synthase
    d) Neuraminidase
    Answer: b) Dihydrofolate reductase
  13. Which organelle is involved in both beta-oxidation of fatty acids and ketone body production?
    a) Mitochondria
    b) Lysosome
    c) Golgi body
    d) Cytosol
    Answer: a) Mitochondria
  14. Which of the following is a fat-soluble vitamin?
    a) Vitamin C
    b) Vitamin B12
    c) Vitamin A
    d) Vitamin B6
    Answer: c) Vitamin A
  15. Which enzyme is inhibited by dicoumarol, interfering with blood clotting?
    a) Neuraminidase
    b) Vitamin K epoxide reductase
    c) HMG-CoA reductase
    d) Xanthine oxidase
    Answer: b) Vitamin K epoxide reductase
  16. Which amino acid is a precursor for serotonin synthesis?
    a) Tyrosine
    b) Tryptophan
    c) Phenylalanine
    d) Arginine
    Answer: b) Tryptophan
  17. What is the primary function of pyrimidine synthesis in cells?
    a) ATP production
    b) DNA and RNA synthesis
    c) Protein degradation
    d) Lipid metabolism
    Answer: b) DNA and RNA synthesis
  18. Which vitamin deficiency causes night blindness?
    a) Vitamin A
    b) Vitamin D
    c) Vitamin E
    d) Vitamin K
    Answer: a) Vitamin A
  19. Which coenzyme transfers one-carbon groups in metabolic reactions?
    a) Coenzyme-A (CoA)
    b) Biotin
    c) Tetrahydrofolate (FH4)
    d) Pyridoxal Phosphate (PLP)
    Answer: c) Tetrahydrofolate (FH4)
  20. Which enzyme is involved in heme degradation to form biliverdin?
    a) Catalase
    b) Cytochrome oxidase
    c) Heme oxygenase
    d) Peroxidase
    Answer: c) Heme oxygenase

This set of MCQs covers crucial concepts from biochemistry relevant for various pharmacy-related exams. It includes questions on vitamins, enzymes, metabolic pathways, competitive inhibition, and more to provide a comprehensive practice set for candidates preparing for GPAT, NIPER, Pharmacist, Drug Inspector, and NPLEX exams.

Also, Visit:

B. Pharma Previous Year Question Paper

B. Pharma Handwritten Notes

B. Pharma PDF Books

B. Pharma Lab Manual

D. Pharma Lab Manual

B. Pharma 8th Semester Previous Year Question Paper

D. Pharma Notes

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