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BP202TSemester 23 creditsTheory

Biochemistry

Complete unit-wise syllabus for BP202T as per the PCI B.Pharm NEP 2020 curriculum (Semester 2 — Organic Chemistry + Biostatistics).

All Sem 2 Subjects
URL:https://pharmacode.vercel.app/syllabus/semester-2/bp202t-biochemistry/

Unit-wise Syllabus

5 Units
1
Enzymology and Clinical Chemistry10 Hours
  • Introduction, properties, nomenclature, IUB classification of enzymes and coenzymes; enzyme kinetics (Michaelis plot, Lineweaver-Burk plot); enzyme inhibitors; regulation: induction, repression, allosteric regulation
  • Therapeutic and diagnostic applications of enzymes and isoenzymes; factors affecting enzyme activity
  • Digestion and absorption of dietary macro- and micronutrients including vitamins and minerals; biochemical functions of vitamins and associated diseases
  • Clinical chemistry: liver function tests; renal function tests; ELISA test
2
Carbohydrate Metabolism and Bioenergetics10 Hours
  • Introduction to biomolecules: carbohydrates, lipids, nucleic acids, amino acids, and proteins
  • Bioenergetics: free energy, enthalpy, entropy; redox potential; energy-rich compounds (ATP, GTP) and biological significance
  • Carbohydrate metabolism: glycolysis, TCA cycle, gluconeogenesis, HMP shunt, glycogen metabolism; regulation of blood glucose; metabolic adaptations in fed state, fasting, starvation
  • Metabolic derangements in diabetes mellitus; Electron Transport Chain (ETC), oxidative phosphorylation, ATP synthesis
3
Lipid Metabolism7 Hours
  • Classification, functions, and properties of lipids and lipoproteins (HDL, LDL, VLDL, chylomicrons)
  • β-oxidation and de-novo synthesis of fatty acids; ketone bodies: synthesis, utilization, and clinical significance
  • Biological significance of cholesterol and lipid profile; disorders: hyperlipidaemias, hypercholesterolaemia, lipid storage diseases, atherosclerosis, fatty liver disease, obesity
4
Amino Acid and Protein Metabolism10 Hours
  • Classification and biological functions of amino acids; structure and functions of proteins and plasma proteins
  • General metabolism: transamination, oxidative and non-oxidative deamination, decarboxylation; urea cycle — nitrogen disposal and detoxification
  • Catabolism of specific amino acids; disorders: phenylketonuria, albinism, alkaptonuria, tyrosinemia, inborn errors of metabolism
5
Nucleic Acid Metabolism and Genetic Information Transfer8 Hours
  • Nucleotide metabolism and related disorders: biosynthesis and catabolism of purine and pyrimidine nucleotides; hyperuricaemia, gout, Lesch-Nyhan syndrome
  • DNA replication: enzymes and mechanism; transcription; translation: genetic code, ribosomes, post-translational modifications
  • Recombinant DNA technology in pharmacy: restriction enzymes, cloning vectors, PCR, applications in drug production

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