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TPI catalyzes the transfer of a hydrogen atom from carbon 1 to carbon 2, an intramolecular reaction<ref>http://en.wikipedia.org/wiki/Oxidation_reduction oxidation-reduction</ref>. This isomerization of a ketose to an aldose proceeds through an ''cis''-enediol(ate) intermediate. This isomerization proceeds without any cofactors and the enzyme confers a 10<sup>9</sup> rate enhancement relative to the nonenzymatic reaction involving a chemical base (acetate ion).<ref>PMID:2043623</ref>
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TPI catalyzes the transfer of a hydrogen atom from carbon 1 to carbon 2, an intramolecular reaction<ref>http://en.wikipedia.org/wiki/Oxidation_reduction</ref>. This isomerization of a ketose to an aldose proceeds through an ''cis''-enediol(ate) intermediate. This isomerization proceeds without any cofactors and the enzyme confers a 10<sup>9</sup> rate enhancement relative to the nonenzymatic reaction involving a chemical base (acetate ion).<ref>PMID:2043623</ref>
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==References==
==References==
<references/>
<references/>

Current revision

TPI catalyzes the transfer of a hydrogen atom from carbon 1 to carbon 2, an intramolecular reaction[1]. This isomerization of a ketose to an aldose proceeds through an cis-enediol(ate) intermediate. This isomerization proceeds without any cofactors and the enzyme confers a 109 rate enhancement relative to the nonenzymatic reaction involving a chemical base (acetate ion).[2]

References

  1. http://en.wikipedia.org/wiki/Oxidation_reduction
  2. Davenport RC, Bash PA, Seaton BA, Karplus M, Petsko GA, Ringe D. Structure of the triosephosphate isomerase-phosphoglycolohydroxamate complex: an analogue of the intermediate on the reaction pathway. Biochemistry. 1991 Jun 18;30(24):5821-6. PMID:2043623

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Eran Hodis

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