BBI501

Recombinant DNA Technology

L-T-P3-1-0 Credits4 Session2026-27 TypeTheory
Appears in 1 semester

B.Tech Bioinformatics · Sem 5 (Core)

Syllabus

5 units · 40 lecture hours
Unit1

Unit 1: VECTORS AND INSERT

8 hrs

Vehicles for gene cloning - Biology of plasmids, Plasmid based vectors, Bacteriophage, Phage vectors, Cosmids, Phasmids, BAC and YAC vectors; Insert preparation- Restriction Digestion-Restriction enzymes, Polymerase chain reaction –Polymerase, Creation of restriction site by PCR.

Unit2

Unit 2: CLONING TECHNIQUE

8 hrs

Ligation –Ligase, cohesive, Blunt end ligation; Other Modification enzymes – Nucleases, Phasphatase, Kinase; Transformation-Preparation of competent cell, chemical and electrical transformation; Transfection; Recombinant selection and screening -Blotting technique.

Unit3

Unit 3: CONSTRUCTION OF GENE LIBRARIES

8 hrs

Construction of cDNA library- construction subtractive cDNA library – construction of genomic DNA library – BAC library – YAC library.

Unit4

Unit 4: EXPRESSION OF RECOMBINANT PROTEIN IN E. COLI

8 hrs

Plasmid expression vectors-general features, promoters used in expression vectors -cloning of genes in correct reading frame in expression vector- purification of recombinant protein using Histidine tag, GST tag, chitin.

Unit5

Unit 5: APPLICATION OF DNA TECHNOLOGY

8 hrs

Applications of rDNA technology in Diagnostics and Therapeutics - HIV diagnosis, Human Insulin, Growth hormone; Recombinant Vaccines, Agricultural Technologies - Golden rice, Insect resistant crops, Genome Editing Tools using CRISPR Cas9 – Principle mechanism application ethics; Artificial Intelligence Application in RDT. Dr. A.P.J. Abdul Kalam Technical University, Lucknow, Uttar Pradesh

Course Outcomes (COs)5 outcomes

After completion of the course student will be able to:

  1. CO1Understand vectors and insert preparation (plasmids, phages, cosmids, BAC, YAC; restriction digestion, PCR).K2
  2. CO2Apply cloning techniques (ligation, modification enzymes, transformation, transfection, and screening).K3
  3. CO3Construct gene libraries (cDNA, subtractive cDNA, genomic, BAC, YAC).K3
  4. CO4Apply methods for expression of recombinant proteins in E. coli (expression vectors, promoters, reading frame, purification tags).K3
  5. CO5Understand the applications of DNA technology in diagnostics, therapeutics, agriculture, and genome editing, including AI-based rapid diagnostic technologies.K2

TEXT BOOKS

  1. / REFERENCES
  2. Jerney D. Wale and Malcolm Von Schants, “From Genes to Genomes: Concepts and Applications of DNA Technology”, John Wiley & Sons, 2002.
  3. Sandy B. Primrose, Richard M. Twyman, “Principles of gene manipulation”, 7th edition, Blackwell Publishing, 2006.
  4. T A Brown, Gene cloning and DNA analysis, 6th edition, Blackwell Publishing, 2010. Dr. A.P.J. Abdul Kalam Technical University, Lucknow, Uttar Pradesh

Official AKTU syllabus

This subject is on page 5, 6, 7 of the original AKTU PDF.

Official AKTU syllabus PDF ↗