Sunday, 25 April 2021

Recombinant DNA Technology: Revolution in Modern Biotechnology

Recombinant DNA Technology: Revolution in Modern Biotechnology

Introduction

Recombinant DNA (rDNA) technology is one of the most powerful and transformative tools in modern biotechnology. It allows scientists to combine DNA from different organisms to create new genetic combinations that do not exist in nature. This technology has revolutionized medicine, agriculture, industry, and research by enabling the production of valuable proteins, improved crops, and disease-resistant organisms.

In simple words, recombinant DNA technology is like “genetic engineering,” where useful genes are inserted into another organism to give it new and beneficial properties.

Discovery of Recombinant DNA Technology

The foundation of recombinant DNA technology was laid in the early 1970s by scientists Stanley Cohen and Herbert Boyer. They successfully transferred a gene from one bacterium into another using plasmids (small circular DNA molecules).

This breakthrough experiment marked the birth of genetic engineering and opened the doors to modern biotechnology. Since then, rDNA technology has grown rapidly and become a core tool in biological research.

Goals and Objectives of rDNA Technology

The main objectives of recombinant DNA technology include:

  • Producing useful proteins like insulin and vaccines
  • Improving crop quality and resistance
  • Understanding gene function
  • Treating genetic diseases
  • Creating industrial enzymes

Basic Steps of Recombinant DNA Technology

The process of rDNA technology involves the following key steps:

1. Isolation of Desired Gene

A useful gene is identified and cut from the donor organism using restriction enzymes (molecular scissors).

2. Selection of Vector

A plasmid or viral DNA is chosen as a carrier (vector) to transport the gene into a host cell.

3. Cutting and Joining

Both the gene of interest and the vector are cut using the same restriction enzyme and then joined using DNA ligase.

4. Transformation

The recombinant plasmid is inserted into a host organism, usually bacteria like E. coli.

5. Multiplication and Expression

The host cell multiplies and starts producing the desired protein.

Key Enzymes Used in rDNA Technology

Some important enzymes include:

  • Restriction enzymes – cut DNA at specific sites
  • DNA ligase – joins DNA fragments
  • DNA polymerase – copies DNA
  • Reverse transcriptase – makes DNA from RNA

Applications of Recombinant DNA Technology

1. Medical Applications

  • Production of human insulin for diabetes
  • Growth hormones
  • Blood clotting factors
  • Vaccines
  • Gene therapy for genetic disorders

2. Agricultural Applications

  • Development of pest-resistant crops
  • Herbicide-resistant plants
  • Drought-tolerant varieties
  • Improved nutritional value of food

Example: Golden rice enriched with Vitamin A.

3. Industrial Biotechnology

  • Production of enzymes for detergents
  • Biofuels
  • Bioplastics
  • Waste treatment

4. Environmental Uses

  • Bioremediation of polluted soil and water
  • Degradation of toxic chemicals

5. Fun and Novel Applications

  • Fluorescent fishes like GloFish
  • Glow-in-the-dark organisms used in research

Advantages of rDNA Technology

  • Increases food production
  • Helps cure diseases
  • Reduces chemical pesticide use
  • Produces life-saving medicines
  • Improves quality of life

Limitations and Ethical Concerns

Despite its benefits, rDNA technology raises concerns such as:

  • Environmental risks
  • Ethical issues
  • Genetic contamination
  • Biosafety problems

Therefore, strict regulations are required.

Conclusion

Recombinant DNA technology is a cornerstone of modern biotechnology. It has transformed healthcare, agriculture, and industry. With responsible use and proper regulation, this technology can greatly benefit humanity in the future.

 

CSIR NET rDNA Quiz with Timer

CSIR NET Interactive Quiz — Recombinant DNA Technology

Time Left: 10:00

Instruction: Attempt all questions before time runs out.

1) DNA ligase joins DNA fragments.
DNA polymerase
RNA polymerase
DNA ligase
Restriction enzyme
2) Restriction enzymes recognize:
Random sequence
Palindromic sequence
mRNA
tRNA
3) Most common vector is:
Chromosome
Plasmid
Ribosome
Histone
4) Best host in rDNA is:
Bacillus
E. coli
Yeast
Fungus
5) DNA cutting enzyme:
Ligase
Restriction enzyme
Helicase
Polymerase
6) Sticky ends produced by:
Blunt cut
EcoRI
Polymerase
Ligase
7) DNA from RNA made by:
Reverse transcriptase
Ligase
Helicase
Endonuclease
8) Selectable marker helps to:
Kill bacteria
Select transformants
Break DNA
Identify host
9) Common selectable marker:
Antibiotic resistance gene
Insulin gene
Histone
rRNA
10) Golden rice enriched with:
Vitamin A
Vitamin C
Iron
Protein

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