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Principles of genetic
engineering
What is genetic engineering
• Genetic engineering, also known as
recombinant DNA technology, means altering
the genes in a living organism to produce a
Genetically Modified Organism (GMO) with a
new genotype.
• Various kinds of genetic modification are
possible: inserting a foreign gene from one
species into another, forming a transgenic
organism; altering an existing gene so that its
product is changed; or changing gene
expression so that it is translated more often
or not at all.
Basic steps in genetic engineering
1. Isolate the gene
2. Insert it in a host using a vector
3. Produce as many copies of the host as
possible
4. Separate and purify the product of
the gene
Step 1: Isolating the gene
Step 1: Alternative method (using
reverse transcriptase)
• Reverse transcriptase
• mRNA converted into cDNA
• Complementary strand produced using
DNA polymerase
• Advantage – more mRNA in cell than
DNA
Step 2: Inserting gene into
vector
• Vector –
molecule of
DNA which is
used to carry a
foreign gene
into a host cell
Step 3: inserting vector into host
• See worksheet
Replica plating
Step 4: Multiplication of the host
cells by cloning
• Large scale fermenters by cloning
• All genetically identical because of
asexual reproduction
Step 5: Extraction of desired
gene product

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genetic engineering !10_52_50_AM (3).ppt

  • 2. What is genetic engineering • Genetic engineering, also known as recombinant DNA technology, means altering the genes in a living organism to produce a Genetically Modified Organism (GMO) with a new genotype. • Various kinds of genetic modification are possible: inserting a foreign gene from one species into another, forming a transgenic organism; altering an existing gene so that its product is changed; or changing gene expression so that it is translated more often or not at all.
  • 3. Basic steps in genetic engineering 1. Isolate the gene 2. Insert it in a host using a vector 3. Produce as many copies of the host as possible 4. Separate and purify the product of the gene
  • 4. Step 1: Isolating the gene
  • 5. Step 1: Alternative method (using reverse transcriptase) • Reverse transcriptase • mRNA converted into cDNA • Complementary strand produced using DNA polymerase • Advantage – more mRNA in cell than DNA
  • 6. Step 2: Inserting gene into vector • Vector – molecule of DNA which is used to carry a foreign gene into a host cell
  • 7.
  • 8.
  • 9. Step 3: inserting vector into host • See worksheet
  • 11. Step 4: Multiplication of the host cells by cloning • Large scale fermenters by cloning • All genetically identical because of asexual reproduction
  • 12. Step 5: Extraction of desired gene product