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- W2068555700 abstract "Anewenzymatic acyloin-type condensation betweenpyruvate (or acetoin or methylacetoin) and D-glyceraldehyde was found to be catalyzed by cell-free extracts of a transketolase mutant of Bacillus pumilus IFO 12089. The reaction product (1) was isolated and determined to be 1-deoxy-D- threo-pentulose (d-DTP), which is considered to be a precursor of the five-carbon unit of the thiazole ring thiamine. l-Deoxy-L-threo-pentulose (l-DTP, 2) was synthesized similarly when lglyceraldehyde was used instead of D-glyceraldehyde. The configurations of 1 and 2 were confirmed by reduction to the corresponding 1-deoxy-pentitols. Similar enzyme activities were also detected in cell-free extracts of all the wild-type strains tested of bacteria, actinomycetes, yeasts, and molds. These results suggest that the d-DTP synthesizing enzyme plays an important role in the biosynthesis of the thiazole ring of thiamine in vivo." @default.
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- W2068555700 date "1984-01-01" @default.
- W2068555700 modified "2023-10-17" @default.
- W2068555700 title "Formation of 1-deoxy-D-threo-pentulose and 1-deoxy-L-threo-pentulose by cell-free extracts of microorganisms." @default.
- W2068555700 cites W2062683072 @default.
- W2068555700 doi "https://doi.org/10.1271/bbb1961.48.149" @default.
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