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Biochemistry BPT Bachelor Physiotherapy syllabus topics

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Biochemistry - BPT (Bachelor of Physiotherapy)

Complete Syllabus Overview & Study Notes

Biochemistry is a first-year subject in BPT (100 marks theory, no practical). It forms the molecular foundation for understanding physiology, pharmacology, and pathology in later years.

UNIT I: Protein Structure and Function

1. Amino Acids and pH

  • 20 standard amino acids - structure, classification (nonpolar, polar, acidic, basic)
  • Amino acid isomers (L vs D forms)
  • Ionization, pKa, isoelectric point (pI)
  • Acid-base balance - pH, Henderson-Hasselbalch equation
  • Buffer systems - bicarbonate buffer (most important in blood)
  • Acid-base disturbances: respiratory/metabolic acidosis and alkalosis
Clinical relevance for BPT: Blood gas interpretation, lactic acidosis during exercise, hyperventilation-induced alkalosis in patients

2. Protein Structure

  • Four levels: Primary (sequence), Secondary (alpha-helix, beta-sheet), Tertiary (3D folding), Quaternary (multiple subunits)
  • Supersecondary structures and motifs
  • Protein folding and chaperones
  • Denaturation

3. Globular Proteins - Hemoglobin

  • Structure of hemoglobin (Hb) and myoglobin
  • Oxygen-dissociation curve (sigmoidal vs hyperbolic)
  • Bohr effect (CO2/H+ shifts the curve - key for exercise physiology)
  • Allosteric regulation by 2,3-BPG
  • Minor hemoglobins: HbA1c (used in diabetes monitoring)
  • Hemoglobinopathies: Sickle cell disease, thalassemia
Physiotherapy relevance: O2 transport during exercise, tissue oxygenation in rehabilitation

4. Fibrous Proteins - Collagen & Elastin

  • Collagen: triple helix structure, types (I, II, III), synthesis and cross-linking
  • Collagenopathies: Scurvy (Vit C deficiency), Ehlers-Danlos syndrome, Marfan syndrome
  • Elastin: role in lung and connective tissue recoil
BPT relevance: Connective tissue, tendon/ligament biochemistry directly applies to musculoskeletal physiotherapy

5. Enzymes

  • Enzyme classification (6 classes), active site, cofactors and coenzymes
  • Michaelis-Menten kinetics: Km, Vmax, Lineweaver-Burk plot
  • Enzyme inhibition: Competitive, Non-competitive, Uncompetitive, Irreversible
  • Regulation: allosteric, covalent modification, zymogen activation
  • Clinically important enzymes: CK-MB (heart), AST/ALT (liver), LDH, Alkaline phosphatase
  • Isoenzymes and their diagnostic significance
BPT relevance: Creatine kinase (CK) is a key marker of muscle damage - crucial in monitoring exercise-induced muscle injury and myopathies

UNIT II: Carbohydrate Metabolism

6. Carbohydrate Chemistry

  • Monosaccharides, disaccharides, polysaccharides
  • Glucose, fructose, galactose structures
  • Glycosidic bonds; starch vs glycogen vs cellulose

7. Glycolysis

  • 10 steps: glucose → 2 pyruvate
  • Net yield: 2 ATP, 2 NADH
  • Key enzymes: hexokinase, phosphofructokinase-1 (PFK-1, rate-limiting), pyruvate kinase
  • Regulation of PFK-1 by ATP, AMP, citrate
  • Anaerobic glycolysis → lactate (Cori cycle)
BPT relevance: Lactic acid production during high-intensity exercise; oxygen debt concept

8. TCA Cycle (Citric Acid / Krebs Cycle)

  • Acetyl-CoA enters the cycle
  • 8 steps, produces: 3 NADH, 1 FADH2, 1 GTP per turn
  • Amphibolic nature (anabolic + catabolic)
  • Key enzymes: isocitrate dehydrogenase, alpha-ketoglutarate dehydrogenase

9. Electron Transport Chain (ETC) & Oxidative Phosphorylation

  • Complexes I-IV in inner mitochondrial membrane
  • ATP synthesis via ATP synthase (chemiosmosis)
  • Total ATP yield per glucose: ~30-32 ATP
  • Uncouplers (e.g., DNP), inhibitors (cyanide, CO)

10. Glycogen Metabolism

  • Glycogenesis (synthesis) and glycogenolysis (breakdown)
  • Key enzymes: glycogen synthase, glycogen phosphorylase
  • Liver vs muscle glycogen (different purposes)
  • Glycogen storage diseases (Von Gierke, McArdle, Pompe)
BPT relevance: McArdle's disease causes exercise intolerance and painful cramps - common exam topic

11. Gluconeogenesis

  • Synthesis of glucose from non-carbohydrate precursors (pyruvate, lactate, glycerol, amino acids)
  • Key gluconeogenic enzymes (bypass steps)
  • Occurs in liver and kidney; important during fasting

12. HMP Shunt (Pentose Phosphate Pathway)

  • Produces NADPH (for reductive biosynthesis) and ribose-5-phosphate (for nucleotide synthesis)
  • G6PD deficiency - hemolytic anemia with oxidative stress

UNIT III: Lipid Metabolism

13. Lipid Chemistry

  • Fatty acids: saturated vs unsaturated, essential fatty acids (linoleic, alpha-linolenic)
  • Triglycerides, phospholipids, glycolipids, sterols
  • Lipoproteins: chylomicrons, VLDL, LDL, HDL - structure and function

14. Beta-Oxidation of Fatty Acids

  • Fatty acid activation → acyl-CoA
  • Entry into mitochondria via carnitine shuttle
  • 4-step spiral: each cycle yields 1 acetyl-CoA, 1 FADH2, 1 NADH
  • ATP yield calculation for palmitate (16C)

15. Fatty Acid Synthesis

  • De novo synthesis in cytoplasm
  • Acetyl-CoA → malonyl-CoA (ACC enzyme, rate-limiting)
  • Fatty acid synthase complex
  • Regulation: insulin stimulates, glucagon inhibits

16. Ketone Bodies

  • Formed in liver from acetyl-CoA during fasting/starvation/diabetes
  • Acetoacetate, beta-hydroxybutyrate, acetone
  • Ketosis vs ketoacidosis
  • Used as fuel by brain during prolonged fasting

17. Cholesterol Metabolism

  • Synthesis via HMG-CoA reductase (rate-limiting; target of statins)
  • Bile acids, steroid hormones, Vitamin D
  • LDL receptor pathway; familial hypercholesterolemia

UNIT IV: Protein and Amino Acid Metabolism

18. Protein Digestion and Absorption

  • Proteases: pepsin, trypsin, chymotrypsin, carboxypeptidase
  • Amino acid absorption mechanisms

19. Nitrogen Metabolism

  • Transamination (AST, ALT - key liver enzymes)
  • Oxidative deamination (glutamate dehydrogenase)
  • Urea cycle - steps, enzymes, regulation
  • Hyperammonemia and its effects

20. Amino Acid Catabolism

  • Glucogenic vs ketogenic amino acids
  • Phenylalanine metabolism: PKU (phenylketonuria)
  • Tyrosine metabolism: albinism, alkaptonuria
  • Homocysteine metabolism and cardiovascular risk

UNIT V: Molecular Biology

21. DNA Structure and Replication

  • Watson-Crick double helix: base pairing (A-T, G-C)
  • Chargaff's rules
  • Semiconservative replication
  • Key enzymes: DNA polymerase, helicase, ligase, topoisomerase

22. RNA and Transcription

  • Types of RNA: mRNA, tRNA, rRNA
  • RNA polymerase; promoter and terminator sequences
  • Post-transcriptional modifications (capping, poly-A tail, splicing)

23. Translation (Protein Synthesis)

  • Genetic code: codons, anticodons, degeneracy
  • Ribosomes (70S prokaryote, 80S eukaryote)
  • Initiation, elongation, termination
  • Post-translational modifications

24. Mutations and DNA Repair

  • Point mutations, frameshifts, insertions, deletions
  • Repair mechanisms: base excision, nucleotide excision, mismatch repair
  • Xeroderma pigmentosum (NER defect)

UNIT VI: Vitamins and Minerals

25. Fat-Soluble Vitamins (A, D, E, K)

VitaminFunctionDeficiency
A (Retinol)Vision, epithelial integrityNight blindness, xerophthalmia
D (Calciferol)Ca2+ absorption, bone healthRickets (child), Osteomalacia (adult)
E (Tocopherol)AntioxidantHemolytic anemia, neuropathy
K (Phylloquinone)Clotting factors (II, VII, IX, X)Bleeding disorder

26. Water-Soluble Vitamins (B-complex and C)

VitaminCoenzyme formDeficiency
B1 (Thiamine)TPPBeriberi, Wernicke's encephalopathy
B2 (Riboflavin)FAD, FMNCheilosis, corneal vascularization
B3 (Niacin)NAD+, NADP+Pellagra (3 Ds: Diarrhea, Dermatitis, Dementia)
B5 (Pantothenic acid)CoABurning feet syndrome
B6 (Pyridoxine)PLPConvulsions, sideroblastic anemia
B7 (Biotin)CarboxylationsDermatitis, alopecia (raw egg white)
B9 (Folate)THFMegaloblastic anemia, neural tube defects
B12 (Cobalamin)MethylcobalaminMegaloblastic anemia + subacute combined degeneration of spinal cord
C (Ascorbic acid)Antioxidant, collagen hydroxylationScurvy (bleeding gums, petechiae, poor wound healing)
BPT relevance: Vitamin D and bone metabolism is critical for fracture rehabilitation; Vitamin C for collagen/wound healing; B12 for neurological physiotherapy

UNIT VII: Special Topics

27. Hormones and Signal Transduction

  • Receptor types: membrane (GPCRs, tyrosine kinase) vs nuclear
  • Second messengers: cAMP, IP3/DAG, Ca2+
  • Insulin vs glucagon signaling
  • Thyroid hormones and metabolic rate

28. Plasma Proteins

  • Albumin (oncotic pressure, transport)
  • Globulins, fibrinogen
  • Acute phase proteins (CRP, ferritin)

29. Nucleotide Metabolism

  • Purine and pyrimidine synthesis (de novo vs salvage)
  • Gout: uric acid accumulation, allopurinol treatment
  • HGPRT deficiency: Lesch-Nyhan syndrome

High-Yield Topics for BPT Exams

RankTopicWhy Important
⭐⭐⭐Collagen & fibrous proteinsMusculoskeletal physio directly
⭐⭐⭐Hemoglobin & O2 transportExercise physiology
⭐⭐⭐Enzyme kineticsPharmacology link
⭐⭐⭐Glycolysis + lactic acidExercise biochemistry
⭐⭐⭐Vitamins (D, C, B12)Clinical deficiencies in rehab patients
⭐⭐⭐Urea cycleLiver function
⭐⭐Beta-oxidationEnergy during prolonged exercise
⭐⭐Glycogen storage diseasesMcArdle's in exercise-intolerant patients
⭐⭐DNA replicationMolecular basis
⭐⭐Cholesterol/lipoproteinsCardiovascular risk

Recommended Textbooks

  1. Lippincott Illustrated Reviews: Biochemistry (Ferrier) - 8th Ed - Best for BPT; clinical correlations
  2. Harper's Illustrated Biochemistry - 32nd Ed - Detailed and comprehensive
  3. Basic Medical Biochemistry: A Clinical Approach (Lieberman & Peet) - Clinically oriented
  4. U.N. Satyanarayana Biochemistry - Popular in Indian universities for BPT/BPharm

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