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Title: Pyruvate is a by-product of Rubisco catalysis

Conference · · Plant Physiology, Supplement; (USA)
OSTI ID:5724846
;  [1]
  1. Australian National Univ., Canberra (Australia)

The catalytic mechanism of D-ribulose-1,5-bisphosphate (RuBP) carboxylase (Rubisco) involves several enzyme-bound intermediates. The 2,3-enediol resulting from abstraction of the C-3 proton from RuBP, and the 6-carbon intermediate resulting from its carboxylation, are well established. However, the C-2 carbanion form of 3-phosphoglycerate, thought to be produced by scission of the bond between C-2 and C-3 of the gem-diol form of the 6-carbon intermediate, is less well documented. We have observed the formation of ({sup 14}C)pyruvate during catalysis by purified spinach Rubisco in the presence of {sup 14}CO{sub 2} to an extent of approximately 1% of the total {sup 14}C fixed at substrate saturation and pH 8. Pyruvate formation was also continuously measured spectrophotometrically in the presence of lactate dehydrogenase and NADH. No pyruvate was formed when 3-phosphoglycerate was substituted for RuBP or when Rubisco was inhibited by a reaction-intermediate analog. Pyruvate is the expected product of {beta}-elimination of the phosphoryl moiety of the acid carbanion, either at the active site or in solution after release from the enzyme. These observations establish the intermediacy of the carbanion species and provide yet another example of Rubisco's catalytic inefficiency.

OSTI ID:
5724846
Report Number(s):
CONF-9007196-; CODEN: PPYSA
Journal Information:
Plant Physiology, Supplement; (USA), Vol. 93:1; Conference: Annual meeting of the American Society of Plant Physiologists, Indianapolis, IN (USA), 29 Jul - 2 Aug 1990; ISSN 0079-2241
Country of Publication:
United States
Language:
English