1. Polymerase Chain Reaction
PCR
Polymerase Chain Reaction

2. PCR Is a revolutionary method developed by Kary Mullis in1983.
PCR is used in molecular biology to make many copies of small sections of DNA.
It is based on the ability of DNA polymerase to synthesize new strand of DNA complementary to a template strand.

3. Because DNA polymerase can only add a nucleotide onto a preexisting 3'-OH group, it needs a primer to which it can add the first nucleotide.
This requirement makes it possible to delineate a specific region of template sequence that the researcher wants to amplify.
At the end of the PCR reaction, the specific sequence will be accumulated in billions of copies, called amplicons.

4. Kary B. Mullis The Nobel Prize in Chemistry 1993
"for contributions to the developments of methods within DNA-based chemistry" "for his invention of the polymerase chain reaction (PCR) method”

5. Taq polymerase

6. Enzymes are proteins that speed up reactions without being consumed themselves.
The most important enzyme in a PCR reaction is called taq polymerase.
A polymerase is an enzyme that attaches molecules together (i.e nucleotides).
Every cell that has DNA has its own polymerase that takes care of replication of DNA.
PCR uses a polymerase from a species of bacteria, Thermus aquaticus, which normally lives in hot springs.

7. Thermus aquaticus

8. Thermal Cycler
Is a laboratory apparatus used to amplify segments of DNA via PCR).
The device has a thermal block with holes where tubes holding the reaction mixtures can be inserted.
The cycler then raises and lowers the temperature of the block in pre-programmed steps.

9. Materials of PCR target DNA Taq DNA polymerase 2 Primers
~20 nucleotides in length
Forward and reverse
the four DNTP’S
Adenine
Thymine
Cytosine
Guanine
cofactor MgCl2.

10. Locate the Target Sequence
Scientists determine which GENE they are interested in studying.
Locate Primers at the beginning and end of gene.

11. Step 1 Denaturing 60 seconds @ 94°C.
Hydrogen bonds between bases break, & backbones separate.

12. Step 2 Annealing 60 seconds @ 60°C.
Forward and reverse primers bond to template DNA.

13. Taq Polymerase
Once primers anneal, Taq Polymerase can attach to them.

14. Step 3 Extension 2 minute at 72°C.
Taq Polymerase adds DNTP’s to complete the DNA copy.

16. The exponential amplification of the
gene in PCR.

17. Amplification

18. Cycle 3
Obtain two copies of target DNA

19. Cycle 30
1,073,741,764
target copies

20. Is there a gene copied during PCR
and is it the right size ?

21. Applications of PCR
A quick, reliable method for detecting all manner of mutations associated with genetic disease.
Duchene muscular dystrophy
Detect unwanted Genetic material
Bacterial or viral infection (HIV).
Amplify degraded DNA samples
Egyptian mummy
Termite in amber