WHAT IS rDNA TECHNOLOGY?
• Is a deliberate and directional manipulation of the genetic make up of a
cell or organism in a pre determined way for producing a genetically
altered cell or organism.
• It is the manipulation of genes in a desired manner under controlled
conditions.
• Also known as gene splicing, gene manipulation or genetic modification.
MAJOR GOALS OF RDNA TECHNOLOGY:
 Formation of gene library
 Identification, isolation and amplification of desired genes
 Study of the expression of specific genes.
 Study of the regulation of expression of selected genes
 Alteration and modifications in the genetic make up of cell or organisms.
 Alteration in the pattern of gene expression.
STEPS INVOVLED IN RDNA CONSTRUCTION
1. Isolation of DNA:Enzymes such as cellulase (plant cells), lysozyme
(bacteria) and chitinase (fungi) are used to isolate pure DNA from the
cells.
2. Fragmentation of DNA:The isolated and purified DNA is treated with
restriction endonucleases which cut the DNA into fragments.
3. Amplification of Gene of Interest: Polymerase chain reaction (PCR) is
a process to amplify the gene once the proper gene of interest has been
cut using the restriction enzymes. Through this process, multiple
copies of the gene of interest can be produced.
4. Insertion of recombinant DNA into the host: The desired dna is inserted
into the host dna with the help of various enzymes
QUESTIONS:
Q1. What is rDNA technology? What are the major goals of this
technology?
OR
Define rDNA technology and list the major goals.
Q2. List out the major steps involved in the rDNA construction.

rDna technology

  • 2.
    WHAT IS rDNATECHNOLOGY? • Is a deliberate and directional manipulation of the genetic make up of a cell or organism in a pre determined way for producing a genetically altered cell or organism. • It is the manipulation of genes in a desired manner under controlled conditions. • Also known as gene splicing, gene manipulation or genetic modification.
  • 3.
    MAJOR GOALS OFRDNA TECHNOLOGY:  Formation of gene library  Identification, isolation and amplification of desired genes  Study of the expression of specific genes.  Study of the regulation of expression of selected genes  Alteration and modifications in the genetic make up of cell or organisms.  Alteration in the pattern of gene expression.
  • 5.
    STEPS INVOVLED INRDNA CONSTRUCTION 1. Isolation of DNA:Enzymes such as cellulase (plant cells), lysozyme (bacteria) and chitinase (fungi) are used to isolate pure DNA from the cells. 2. Fragmentation of DNA:The isolated and purified DNA is treated with restriction endonucleases which cut the DNA into fragments. 3. Amplification of Gene of Interest: Polymerase chain reaction (PCR) is a process to amplify the gene once the proper gene of interest has been cut using the restriction enzymes. Through this process, multiple copies of the gene of interest can be produced.
  • 6.
    4. Insertion ofrecombinant DNA into the host: The desired dna is inserted into the host dna with the help of various enzymes
  • 8.
    QUESTIONS: Q1. What isrDNA technology? What are the major goals of this technology? OR Define rDNA technology and list the major goals. Q2. List out the major steps involved in the rDNA construction.