To use all functions of this page, please activate cookies in your browser.
With an accout for my.bionity.com you can always see everything at a glance – and you can configure your own website and individual newsletter.
- My watch list
- My saved searches
- My saved topics
- My newsletter
Taq polymerase is a thermostable DNA polymerase named after the thermophilic bacterium Thermus aquaticus from which it was originally isolated. It is normally abbreviated to "Taq Pol," or simply "Taq", and frequently used in polymerase chain reaction.
Additional recommended knowledge
T. aquaticus is a bacterium that lives in hot springs and hydrothermal vents, and Taq was identified as an enzyme able to withstand the protein-denaturing conditions, namely, high temperature, required during PCR. Therefore it replaced E.coli DNA polymerase in PCR. Taq's temperature optimum for activity is 75-80°C with a halflife of 9 min at 97.5°C. 
One of Taq's drawbacks is its low replication fidelity since it lacks a 3' to 5' exonuclease proofreading activity; thus it has an error rate of about one in 9,000 nucleotides.  It can amplify a 1-kb strand of DNA in roughly 30-60 seconds at 72°C. Some thermostable DNA polymerases, such as Pfu DNA polymerase that have been isolated from other thermophilic bacteria possess 3'-5'exonuclease proofreading activity and are being used instead of, or in combination with, Taq in PCR for high-fidelity amplification of DNA.
Taq yields DNA products that have A (Adenine) overhangs at their 3' ends. This is may be useful in 'TA Cloning,' whereby a cloning vector (such as a plasmid) is used which has a T (Thymine) 3' overhang, which complements with the A overhang of the PCR product, thus enabling ligation of the PCR product into the plasmid vector.
|This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Taq_polymerase". A list of authors is available in Wikipedia.|