1. Genetic Engineering

2. “In Greek mythology, the chimera was part lion, part goat, part serpent, which was slain by the hero Bellerephon. In modern day biology, a chimera is a genetically engineered creature created from the DNA of different species. What once was fiction has now become fact; through the process known as DNA recombinant research, scientists are able to splice genes together from different species that would never be able to mate under normal, non-laboratory circumstances. “ Linda MacDonald Glenn

3. What is Genetic Engineering? Involves the manipulation of DNA in order to alter the trait(s) of an organism. Used in: - genetically modified foods -make crops pest resistant -make crops more frost/drought resistant -mass production of human proteins such as growth hormone and insulin - more examples

4. Bacteria are very useful in genetic engineering for their ability to pick up free DNA in their environment. This process is known as TRANSFORMATION. Transformation requires the presence of PLASMIDS – circular pieces of DNA that exist in some bacteria cells. Plasmids exist outside the main bacterial chromosome and carry their own genes – often genes that confer resistance to antibiotics and are capable of self replication.

6. How are Plasmids Used in Transformation?

7. Steps in Transformation Experiments 1.A restriction enzyme is used to cut the genes of interest (a section of DNA) from the foreign DNA 2.The same RE is used to cut the plasmid at the specific recognition site for the RE – the plasmid is now linear 3.The RE used will generate sticky ends in both the foreign and plasmid DNA. Placing the cut foreign DNA in the same solution as the cut plasmid will cause the sticky ends of the foreign and plasmid DNA to anneal (join) - creating a recombinant DNA molecule 4.The resulting piece of recombinant DNA is then introduced into a bacterium. A bacterium that has taken up foreign DNA is referred to as being transformed.

8. How do bacteria cells take in genetically engineered plasmids? The bacteria cells need to be made “competent” – need to readily take up foreign DNA. Cells are made competent by placing them in a cooled solution of CaCl 2. The Ca 2+ ions interact with negatively charged phosphate group on phospholipid head stabilizing the cell membrane. The cold temperature makes the membrane less fluid. The cells are then heat shocked (at ~ 40°C) for a few seconds. This temperature difference (between inside/outside of the cells) creates a draft which sweeps the engineered plasmid into the bacteria cell. Engineered Plasmid DNA is copied whenever bacterial cells reproduce.

9. Animation of plamid cloning http://www.sumanasinc.com/webcontent/a nimations/content/plasmidcloning.htmlAnimation of plamid cloning http://www.sumanasinc.com/webcontent/a nimations/content/plasmidcloning.html Animation of plasmid uptake http://www.dnalc.org/view/15918- Transformation.htmlAnimation of plasmid uptake http://www.dnalc.org/view/15918- Transformation.html

10. How do you know if the bacteria cells were transformed? If you grow the bacteria on a nutrient agar plate that contains an antibiotic, only the transformed bacteria will survive and express the gene of interest (such as the “glow in the dark” gene). All other bacteria that do not contain the plasmid (and the antibiotic resistance gene) will not survive.