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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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Moving Genes

  Adding a new gene to a cell is called transformation. The new DNA has to get into the nucleus of cell. To do this, it has to get through the cell membrane and cell wall that protect the cells and their contents, and finally through the nuclear membrane.

New genes can be inserted into plant, animal and bacterial cells in several different ways.

 
 

Transferring genes to bacteria

  To transform bacteria such as Escherichia coli, two common methods are used – calcium chloride treatment and electroporation.

Calcium chloride treatment involves placing the bacteria and the bacteria with the new gene in them in an ice-cold solution containing calcium chloride.

The calcium chloride changes the nature of the cell wall, allowing the new DNA to enter the cells more easily. The cells are then 'heat shocked' by heating to 42°C in a waterbath for 2 minutes. The heat shock causes the cells to take up the plasmid with the new DNA.

The cells are returned to normal growing conditions so that they can recover and the new gene begins to function within the cell.

 
 

Transferring genes to plants

  The most commonly used method is to use a bacterium called Agrobacterium tumefaciens as a carrier of the new gene. This bacteria naturally infects plant cells, forming crown galls - large tumour-like swellings at the crown of the plant, just above soil level.

The new DNA is first transferred to the circular DNA molecules called plasmids which are found within bacteria. When the bacteria infects the plant cells, the new DNA enters the plant cell.

 
 

Transferring genes to plant, animal and yeast cells

  Electroporation can be used to transform cells of animals, yeast, plants and bacteria. Plant cells are first treated to remove their cell walls. Animal cells don’t have cell walls, so don’t require this first step.

The cells are placed in a solution with the new DNA that is to be added. The solution is then subjected to a high voltage electric shock for a fraction of a second. This causes small holes to form in the cell membrane, through which DNA can enter.

The cells are then placed in a nutrient solution, allowing them to repair their membranes and cell walls and recover their normal functions.

 
 

Transferring genes to egg cells

  The most commonly used method to transfer DNA directly into animal cells such as egg cells is to inject the DNA directly into a newly- fertilised egg cell using a glass capillary tube. This is called microinjection.

The egg cell containing the new DNA is implanted into a female animal. Because the gene was inserted into the DNA at the egg stage, when the cell divides, every cell in the growing embryo will contain the new DNA.

 
 

Other transformation methods

 
  • Calcium phosphate precipitation and phagocytosis: used to transform cells of mammals. Only about 1-2 per cent of cells are transformed, so it is not a particularly efficient procedure. The DNA to be transferred is mixed with calcium phosphate. The DNA and the calcium phosphate react to form tiny solid grains. The cells engulf the grains in a process called phagocytosis (how amoebas eat their food). Some of the new DNA becomes a part of the cell's DNA.
     
  • Lipofection: used to transform cells of animals, yeast, plants and bacteria. Plant cells are first treated to remove their cell walls. The DNA to be transferred is placed into liposomes, which are special kinds of fats that form tiny hollow bubbles. The cells to be transformed are added to the solution containing the liposome bubbles. Since the liposomes are made up of lipids, they become part of the cell membrane of the cells and the contents - the new DNA - enters the cells
  • Biolistics: used widely in the production of genetically modified corn, and also in the genetic immunisation of animals. Tiny tungsten or gold particles are coated with the DNA to be transferred. The particles are usually about 0.004 of a millimetre in diameter. A blast of high-pressure helium gas or gunpowder shoots the particles carrying the DNA into the cells that are to be transformed.
     
  • Viruses as carriers: used to transform cells of plants and animals. It is not a commonly-used technique. A virus is chosen that will enter the cell to be transformed but not kill it. The DNA to be transferred is added to the virus DNA. The virus injects its DNA, including the new DNA, into the cell.
 
   
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