Biotechnology Principles and Processes Class 12 Notes — CBSE Biology Chapter 11

Chapter 11 — Biotechnology: Principles and Processes — covers rDNA technology, tools (restriction enzymes, vectors, host organisms), and processes (PCR, gel electrophoresis, gene cloning). Carries 6-8 marks.

Key Concepts

Principles of Biotechnology

  1. Genetic Engineering: Altering DNA/RNA to modify an organism → recombinant DNA (rDNA) technology
  2. Bioprocess Engineering: Maintaining sterile conditions for large-scale production (bioreactors)

Tools of rDNA Technology

Restriction Enzymes (“Molecular Scissors”)

Cut DNA at specific palindromic recognition sequences
Example: EcoRI recognises 5′-GAATTC-3′ / 3′-CTTAAG-5′
Cuts between G and A → creates sticky ends (overhanging single-stranded regions)
Sticky ends are useful because they can join with complementary sticky ends from another DNA molecule using DNA ligase

Vectors (Vehicles for Gene Transfer)

VectorFeatures
pBR322 (plasmid)Origin of replication (ori), ampᴿ and tetᴿ genes (selectable markers), restriction sites
Ti plasmidFrom Agrobacterium tumefaciens; T-DNA integrates into plant genome
Bacteriophage λHigher capacity than plasmid
BAC, YACFor large DNA inserts (genomic libraries)
Features of an ideal vector: (1) Origin of replication (ori), (2) Selectable marker (antibiotic resistance), (3) Cloning site (restriction enzyme sites), (4) Small size for easy manipulation.

Selectable Markers — Insertional Inactivation

If foreign gene is inserted into a selectable marker gene (e.g., ampᴿ), that gene is inactivated. Recombinants can be identified because they lose that antibiotic resistance.

Newer method: Blue-white screening using lacZ gene and X-gal — recombinants are white (lacZ disrupted), non-recombinants are blue.

Processes of rDNA Technology

PCR (Polymerase Chain Reaction)

Amplifies a specific DNA segment in vitro

Steps (each cycle):
1. Denaturation (94°C): DNA strands separate
2. Annealing (55-65°C): Primers bind to template
3. Extension (72°C): Taq polymerase extends primers → new DNA

After n cycles: 2ⁿ copies of target DNA
Taq polymerase: Thermostable DNA polymerase from Thermus aquaticus (works at high temp)

Gel Electrophoresis

  • Separates DNA fragments by size in agarose gel
  • DNA is negatively charged → moves towards anode (+)
  • Smaller fragments move faster/farther
  • Visualised using ethidium bromide (stains DNA → orange under UV)
  • Separated DNA cut from gel = elution

Gene Cloning Steps

1. Isolation of DNA (gene of interest)
2. Cutting with restriction enzymes (same enzyme for gene and vector)
3. Ligation (gene + vector → rDNA using DNA ligase)
4. Transfer into host cell (transformation, microinjection, biolistics/gene gun)
5. Selection of recombinants (selectable markers)
6. Expression of gene → desired protein

Bioreactors

  • Large vessels (100-1000L) for growing host cells at industrial scale
  • Stirred-tank bioreactor: most common; agitator for mixing, O₂ supply, temperature/pH control
  • Downstream processing: separation, purification of protein product

Quick Revision Points

  • Restriction enzymes: cut at palindromic sequences → sticky ends; EcoRI (GAATTC)
  • Vectors: pBR322 (ori, ampᴿ, tetᴿ); Ti plasmid (Agrobacterium, for plants)
  • Selectable markers identify recombinants (insertional inactivation, blue-white screening)
  • PCR: denature → anneal → extend; Taq polymerase; 2ⁿ copies
  • Gel electrophoresis: DNA moves to +ve electrode; smaller = faster
  • Gene cloning: isolate → cut → ligate → transform → select → express
  • Bioreactors: stirred-tank; downstream processing for purification

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