| Literature DB >> 24333566 |
Claire M Grison1, Brice-Loïc Renard2, Claude Grison2.
Abstract
2-Keto-3-deoxy-D-erythro-hexonic acid (KDG) is the key intermediate metabolite of the Entner Doudoroff (ED) pathway. A simple, efficient and stereoselective synthesis of KDG isopropyl ester is described in five steps from 2,3-O-isopropylidene-D-threitol with an overall yield of 47%. KDG isopropyl ester is studied as an attractive marker of a functional Entner Doudoroff pathway. KDG isopropyl ester is used to promote growth of ammonium producing bacterial strains, showing interesting features in the remediation of heavy-metal polluted soils.Entities:
Keywords: 2-Keto-3-deoxy-D-erythro-hexonic acid isopropyl ester; Entner Doudoroff pathway; Heavy-metal resistant rhizobia; Modified Darzens reaction; One-pot isomerization-reduction reaction; Swern oxidation
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Year: 2013 PMID: 24333566 DOI: 10.1016/j.bioorg.2013.11.006
Source DB: PubMed Journal: Bioorg Chem ISSN: 0045-2068 Impact factor: 5.275