The Discovery of Taq Polymerase and the Invention of PCR

Structure of Taq polymerase
The polymerase chain reaction (PCR) is one of the foundational molecular techniques of modern biology. Making it possible to perform a huge range of standard techniques such as cloning, genotyping, and mRNA quantification.

Today, we often take PCR for granted. Thermocyclers are ubiquitous, various polymerases and kits are commercially available and relatively inexpensive.

But the first iteration of PCR used polymerase purified from E. coli, which couldn't tolerate the high temperature required for denaturation of DNA, and thus had to be added fresh to the reaction after each round of amplification.

The essential breakthrough came when an eccentric chemist named Kary Mullis came up with the idea to try using a polymerase from a thermophilic bacteria, Thermus aquaticus. The use of this Taq polymerase dramatically improved the accuracy and speed of PCR, and ended up winning him the 1993 Nobel Prize in Chemistry.
Additional reading: Mullis is perhaps as famous for his work on PCR as he is for his wild behavior and views.
A good portrait of which can be found here:
NOBEL CHEMIST KARY MULLIS, MAKING WAVES AS A MIND SURFER

Paper on the first purification of Taq polymerase:
Chien et al. 1976. Deoxyribonucleic acid polymerase from the extreme thermophile Thermus aquaticus. 

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