Nature of primary product(s) of D-glucose 6-phosphate dehydrogenase reaction 13C and 31P NMR study

Jarori, Gotam K. ; Maitra, Pabitra K. (1991) Nature of primary product(s) of D-glucose 6-phosphate dehydrogenase reaction 13C and 31P NMR study FEBS Letters, 278 (2). pp. 247-251. ISSN 0014-5793

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Official URL: http://linkinghub.elsevier.com/retrieve/pii/001457...

Related URL: http://dx.doi.org/10.1016/0014-5793(91)80127-O

Abstract

Glucose 6-phosphate dehydrogenase catalyzes the oxidation of glucose 6-phosphate, resulting in the formation of 6-phosphogluconolactone, As this compound is unstable, it has not been characterized directly. NMR provides a way to directly monitor all components of a reaction and study their structure. Here we report some results on the glucose 6-phosphate dehydrogenase reaction using 31P and 13C-NMR. Our results indicate that two different lactones, namely γ (1=4 and δ (1=5) 6-phosphogluconolactones, are formed as products in this reaction. This is in contrast to an earlier suggestion that glucose 6-phosphate dehydrogenase produces only the γ-lactone. On the basis of these results, a new mechanisms for dehydrogenation of the sugar phosphate is proposed.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:D-glucose 6-phosphate Dehydrogenase; Lactone; 13C NMR; 31P NMR
ID Code:31412
Deposited On:25 Apr 2011 09:30
Last Modified:17 May 2016 14:03

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