5 Steps of Genetic Engineering Used in rDNA technology

Genetic engineering is the process of transfer of a desired gene from an organism of interest to an organism of choice to obtain a desired product by applying the principle of biotechnology.

The procedure followed is called the r-DNA technology.

In short, a desired substance is produced by transfer of desired gene (DNA) from parent organism to a different organism.

In most cases the desired organism is human or other organisms of human interest. While the organism of choice is mostly bacteria or yeast.

But why only bacteria and yeast? Because they can be easily grown and also their life cycle completes in few hours to days. Due to this we get the desired product formed in a short time

Because of such short lifespan, they express the transferred gene to the fullest and we obtain the product very fast.

The process occurs in 5 steps as

  1. Isolation of desired gene (gene cloning technology)
  2. Selection of vector
  3. Transfer of r-DNA
  4. Transformation of r-DNA
  5. Identification, isolation & culture of transgenic bacteria# Steps in genetic engineering

1.Isolation of desired gene: Here the DNA or gene from an organism is isolated. This isolated DNA is one which codes for desired protein in the body. This DNA is separated from rest of the gene of the organism by use of DNA lyases.

This is done by three methods

i) Shot gun technique

ii) Complimentary DNA method

iii) Artificial synthesis: This is latest method where the gene is synthesized in the lab. We do not need lyase enzymes here.

The isolated genes are purified and taken for next step to fix to a vector.

2. Selection of vector: Vector is a vehicle to carry the desired gene into the genome of another organism. This helps us to see that the gene is not destroyed during transfer. Also the gene will be operational inside the new organism due to vector. These vectors have some specific properties like

steps in genetic engineering

Photo by: bbc.co.uk

  1. It should be capable of independent multiplication. This is possible if the gene has “Ori gene”
  2. It should have a restriction site i.e. a site where the isolated gene can be fixed using restriction endonuclease. This is also called multiple cloning sites.
  3. Vector should have a gene promoter sequence like β-galactosidase gene.
  4. Should have Marker gene which helps to identify transgenic cells.

There are many types of vectors like

a) Plasmids: These are naturally occurring proteins from bacteria.

b) Cosmids:

c) Phasemid

d) Transposons

e) Bacteriophage (virus)

f) Yeast

g) Shuttle vectors:

These vectors are large pieces of DNA molecules mostly.

Plasmid  is a circular, single stranded and self replicable DNA molecule present inside bacteria. They help in sexual reproduction of bacteria by transfer of genetic matter from one to another. Here we use them to transfer desired gene.

Bacteriophage is a virus which attacks bacteria and inserts its gene into bacterial cell for multiplication. Cosmid is similar to plasmid dna but can accommodate large DNA pieces.

Transposons: These are movable genes or jumping genes which move from one cell to another or plasmid to nucleus. The size is very small like 1kb to 2kb (1kb =1000nucleotide). This transposon has no “marker gene” and “ori gene”

Yeast cloning vector: These are used to transfer the desired gene into fungi. This is similar plasmid with little modification.

Shuttle vector: These vectors have ori-gene, promoter gene for both bacteria and fungi. So it is two in one type.

Diagrammatic representation of the process.production of recombinant protein.

3.Transfer of r-DNA:

The isolated gene is now transferred into the vector in this step. This is done by any of the 4 techniques viz.

  1. Cohesive technique: Here cohesive ends are formed for joining with vector. Restriction endonuclease enzyme is used to cut the desired gene and also plasmid. By this cohesive ends are formed. These cohesive ends in both plasmid and desired gene are easily attachable.Cohesive-ends-1
  2. Homo polymer chain: Here polymers are formed at the ends of gene to fix with vector.Homopolymer-tailing
  3. Blunt end joining. Here the genes with blunt ends are joined to vector by use of DNA ligase enzyme.Blunt-end-Technique
  4. Use of Cos sites. Cos site is one which has 12 nucleotide chains. The vector with gene is transferred into a bacteriophage. As we know bacteriophage is a virus which attacks bacteria and multiplies. So bacteriophages transfer the desired gene loaded vectors.

4. Transformation of r-DNA:

Here the vector with tagged desired gene is transferred into organism of interest i.e. bacteria or fungi in most cases. This is done by creating holes in the bacterial cell wall. For this we use two methods

By use of CaCl2: Here bacteria and calcium chloride are taken in a Petri dish and cooled to 0-4 degrees. Then r-DNA is added and the temperature is suddenly raised to 42degree. When cooled the bacterial wall shrinks and when heated instantly, it expands abnormally creating pores in the wall. The loaded vector enters the cell through these pores.

For those bacteria which do not tolerate this temperature, this method is not used.

By use of lysozymal enzymes: This lysozymal enzyme destroys bacterial cell wall. So this enzyme is taken in low concentration along with plasmids (vector) and added to bacterial culture. The cell wall cracks and plasmids enter. Then the enzyme is removed by centrifugation and supernatant discarding.

By Transduction: Here desired gene is loaded into cosmid and inserted into an empty capsule of virus. The transformed virus is introduced into beaker of E-coli. The transformed virus enters into E-coli by transduction methods.

5. Identification, isolation & culture of transgenic bacteria:

Once the transformation is done, now we need to identify and isolate those bacteria from culture media which have the vector within.

For this few methods are followed like

Antibiotic sensitivity technique: This is based on replica plating method. Here the bacteria with desired gene are isolated on to another media. For this the solution of bacteria is taken and added with antibiotic ampicillin. Those with ampicillin resistance gene multiply. While all those without vector do not grow and are inhibited. The remaining ones grow into visible colonies.

A cylindrical vessel with flat bottom with muslin cloth wound is pressed over those colonies. E colonies get fixed to the cloth which is again touched to the surface of fresh media. Thus the bacteria with r-DNA are isolated. These are grown in culture media in presence of promoter gene to get the desired product.

The above method is not suitable for yeast and virus. So other immunological techniques like nucleic acid hybridization, polymer chain reaction are used.

Direct phenotypic identification: Here transgenic bacteria are identified based on the new developed characters. For example bacteria with β-lactamse producing gene survive the culture media when added with ampicillin while remaining die.

After isolation, the bacteria are cultured by fermentation process to produce the desired product. The culture broth has all the required nutrients. Also it has gene promoters which encourage the tansgenic gene in the bacteria to get activated and produce the product. But why do we need a promoter?

Because all the genes in the genetic material do not activate at all the times. So the transgenic gene needs and external stimuli to produce the m-RNA by transcription. This m-RNA which is coded for desired substance is translated into the protein.

This is how we manufacture many vaccines like hepatitis-B, vitamins like B12, hormones like Insulin etc.

Without this technique we needed to extract them from animals or by other means which was insufficient to market demand. Also the product obtained has compatibility problems with human body as it was from other source. But the product obtained by this method is an exact copy of the one produced in body so it is compatible.

Leave a Reply