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Biosynthesis of Uridine Diphosphate d-Xylose
UDP- d -glucuronic acid labeled with tritium at either C-3, C-4, or C-5 was converted to UDP- d -xylose by UDP-glucuronate carboxy-lyase (EC 4.1.1.35) from wheat germ and Cryptococcus laurentii . A kinetic isotope effect ( V t / V h ) of 0.32 and 0.42 for the C. laurentii and wheat germ enzymes, res...
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Published in: | The Journal of biological chemistry 1970-05, Vol.245 (10), p.2476-2482 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | UDP- d -glucuronic acid labeled with tritium at either C-3, C-4, or C-5 was converted to UDP- d -xylose by UDP-glucuronate carboxy-lyase (EC 4.1.1.35) from wheat germ and Cryptococcus laurentii . A kinetic isotope effect ( V t / V h ) of 0.32 and 0.42 for the C. laurentii and wheat germ enzymes, respectively, was observed with the C-4-labeled substrate but not with the C-3- or C-5-labeled substrate.
Labeled UDP- d -xylose obtained from UDP- d -glucuronic acid-5 T was converted with phosphodiesterase to labeled α- d -xylosyl phosphate. The latter was oxidized with periodic acid to yield d -phosphodiglycolic aldehyde from C-1 and C-2 and from C-4 and C-5; hypobromite oxidation of the dialdehyde yielded d -phosphodiglycolic acid. Acid hydrolysis of this compound released unlabeled glyoxalic acid (which originated from C-1 and
C-2) and labeled glycolic acid (from C-4 and C-5). The latter was converted to unlabeled glyoxalic acid upon oxidation with
glycolic oxidase from spinach, which is specific for that hydrogen atom in glycolic acid sterically equivalent to the α-hydrogen
of l -lactic acid. These results show that the configuration at C-5 changed from S to R during the decarboxylation of UDP- d -glucuronic acid. Since UDP-glucuronate carboxy-lyase requires NAD for activity, these data suggest that the reaction involves
oxidation at C-4 to yield UDP-4-keto- d -glucuronic acid, followed by decarboxylation and formation of UDP-4-keto- d -xylose, which is then stereospecifically protonated at C-5 and reduced at C-4 to yield product. The presence of an isotope
effect with UDP- d -glucuronic acid-4 T means that either the initial oxidation or the final reduction is the rate-limiting step of the reaction; it is not possible
to differentiate between these two possibilities on the basis of the available data. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1016/S0021-9258(18)63095-9 |