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A Scientific Approach To Biotechnology

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A Scientific approch to biotechnology between_pic_1 Biotechnology between_pic_2 Biotechnology Help
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Understanding Biotechnology


What is Biotechnology

Overview of Biotechnology

  Then and Now of Biotechnology
 

History of Biotechnology

  Gene Technology
  What is a gene
  Gene Technology Techniques
  Genetic modification myths
  Genes code for proteins
  What is DNA
  Where is DNA
  The Full Set
  What does DNA look like
  What does DNA work
  DNA Unknown

Why do we do biotechnology?


  Why do we do biotechnology?
  Biotechnology for ourselves

Biotechnology for the environment

Biotechnology for food and agriculture

How do you do biotechnology?

  How do you do biotechnology
Finding the gene you want
  Cutting and pasting genes
  Moving genes
  Reading and interpreting genes
  Cloning a gene
  Cloning plants
  Cloning animals
Biotechnology Applications

  Human Uses
  Fighting infectious diseases
  Antibiotics
  Producing human products
  Reproductive technologies
  The human genome project
  Genetic disorders
  Gene therapy
  Cloning
  Stem cells
  Transplantation
  DNA profiling
  Environment
  Biological control of pests
  Protecting threatened species
  Resurrecting extinct species
  Cleaning up and managing
  Researching new products
  Food and Agriculture
  Feed Me
  A problem with weeds
  A problem with insects
  Other reasons to modify crops
  The international scene
  Genetically modified food labeling
  Health and Medical
  Biotechnology in medicines
  Clinical trials
  Gene therapy
  Genes and cancer
  What are ethics
Benefits & Risks of Biotechnology

  Arguments for and against gene
  A nutritionist's view on GM foods
  Balance sheet 2020
  Sustaining the Food supply
Biotechnology Resources

  Ethics of biotechnology
  Conferences and events
  Forums and Communities
  Biotechnology Websites
  Glossary of terms
   
 
 

 

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Cutting and Pasting Genes

  Genes can be cut out from the DNA of an organism and pasted into a new position in the chromosomes of that organism or a different organism. This cutting and pasting process is called gene splicing.
 
 

Cutting Genes

  One of the basic tools that scientists use to study or transfer segments of DNA is a group of chemicals called restriction enzymes.

Restriction enzymes are like molecular scissors. They are used to cut up DNA. They were originally found in bacteria, where they act as a defence mechanism. The bacterial restriction enzymes recognise foreign DNA, such as from a virus, when it enters a bacterial cell, and inactivates it by cutting it up. The handy thing for scientists is that restriction enzymes do not cut DNA randomly - they cut at very specific places.

Bacterial restriction enzymes will work on DNA from other organisms because DNA is chemically identical, whether it comes from bacteria, a rose or a human. The bases of DNA are always the same; it's just the arrangement of the bases that varies.

Different restriction enzymes cut at different sites. Each restriction enzyme recognises a certain DNA sequence, usually about four to six base pairs long, and cuts the DNA within this sequence. For example, the enzyme EcoRI, which is taken from the human gut bacteria E. coli, recognises the genetic sequence GAATTC. It cuts the DNA between the guanine (G) and the adenine (A).

Some enzymes cut straight through both strands of the DNA molecule to produce 'blunt' ends of DNA. Others cut one strand of the DNA molecule in one spot and the second strand slightly to the left or right. This creates two ends with one strand that hangs slightly over; these are called 'sticky' ends.

When cutting and pasting a gene, researchers usually use the enzymes that cut and produce sticky ends. This allows the overhanging strand of DNA to be easily matched up with another strand of DNA .

 
 

Pasting Genes

  The cut piece of DNA can be pasted either into a new chromosome, or into a plasmid - one of the small circular DNA molecules found in bacteria. Plasmids are used when transferring a gene from one organism to another.

The DNA of the new chromosome or plasmid is usually cut with the same restriction enzyme that was used to cut the gene out. This means the sticky ends will have the same DNA code as the ends of the piece being pasted in. The overhanging strands of DNA bind together, and another enzyme, called ligase, is used to seal the join

 
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