Home
Class 12
BIOLOGY
How bacterial cells are made competent t...

How bacterial cells are made competent to take up DNA?

Text Solution

Verified by Experts

Since, DNA is a hydrophilic molecule, it cannot pass through the cell membrane. In order to force the bacteria to take up the plasmid, the bacterial cells must first be made competent to take up foreign DNA. This is done by treating them with a specific concentration of a divalent cation such as calcium `(Ca^(2+))`, which increases the efficiency with which DNA enters the bacterium through the pores on its cell wall.
Recombinant DNA can then be forced into such cells by incubating the cells with recombinant DNA ice, cold solution of calcium chloride followed by subjecting them briefly into heat shock at `42^(@)C` and then putting them back on `CaCl_(2)` solution. This enables the bacteria to take up the recombinant DNA.
Promotional Banner

Topper's Solved these Questions

  • PRINCIPLES AND PROCESSES OF BIOTECHNOLOGY

    ARIHANT PRAKASHAN|Exercise TOPIC - 1 (PRACTICE QUESTIONS) (7 MARK QUESTIONS) |2 Videos
  • PRINCIPLES AND PROCESSES OF BIOTECHNOLOGY

    ARIHANT PRAKASHAN|Exercise TOPIC TEST 1|10 Videos
  • PRINCIPLES AND PROCESSES OF BIOTECHNOLOGY

    ARIHANT PRAKASHAN|Exercise TOPIC - 1 (PRACTICE QUESTIONS) (2½ MARK QUESTIONS) |12 Videos
  • ORGANISMS AND ENVIRONMENT

    ARIHANT PRAKASHAN|Exercise Chapter Test (7 MARK Questions) |4 Videos
  • REPRODUCTION IN ORGANISMS

    ARIHANT PRAKASHAN|Exercise Chapter Test (7 MARKS Questions) |4 Videos

Similar Questions

Explore conceptually related problems

Genes are made up of :

Plasmids present in bacterial cells are linear double helical DNA molecules.

Nissl's granules are made up of

Read the following statements and select the correct ones. (i) Same kind of sticky ends are produced when a DNA has been cut by different restriction enzymes. (ii) Exonucleases make cuts at specific positions within the DNA. (iii) Hind ll was the first restriction endonuclease to be isolated. (iv) A bacteriophage has the ability to replicate within bacterial cells by integrating its DNA with bacterial DNA. (v) Presence of more than one recognition sites for a enzyme within the vector facilitates the gene cloning.