ChemInform Abstract: 5-Hydroxypentane-2,3-dione (Laurencione), a Bacterial Metabolite of 1-Deoxy-D-threo-pentulose
Autor: | Albert Boronat, Michel Rohmer, Narciso Campos, Knut Danielsen, Surya Rosa Putra, Lionel Charon, Catherine Pale-Grosdemange, Luisa Maria Lois |
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Rok vydání: | 2010 |
Předmět: | |
Zdroj: | ChemInform. 29 |
ISSN: | 1522-2667 0931-7597 |
DOI: | 10.1002/chin.199845214 |
Popis: | Cell-free systems from the bacteria Escherichia coli and Klebsiella planticola that were incubated with 13 C labeled pyruvate and D-glyceraldehyde synthesized 5-hydroxypentane-2,3-dione (laurencione) along with 1-deoxy-D- threo -pentulose (1-deoxy-D-xylulose). Both compounds showed identical labeling patterns, indicating that the C 5 skeletons were derived from the condensation of (hydroxyethyl)thiamin on D-glyceraldehyde. Conversion of [5,5- 2 H 2 ]deoxyxylulose into laurencione by a cell-free system from E. coli showed that the α-dione is obtained from the pentulose by water elimination. |
Databáze: | OpenAIRE |
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