Incorporation of 2-C-Methyl-d-erythritol, a Putative Isoprenoid Precursor in the Mevalonate-Independent Pathway, into Ubiquinone and Menaquinone of Escherichia coli
✍ Scribed by Tore Duvold; Patrizia Calí; Jean-Michel Bravo; Michel Rohmer
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 802 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Incorporationofdeutenum labelled2-C-metbyl-D-erytbritOl into isoprenoidside-chains of ubiquinoneandmenaquinonefromEscherichiocoli.stronglysupports theproposedintermediaterole of this branchedsugar derivativein the mevalonateindependentpathwayfor isoprenoidbiosynthesis via glycemfdehyde 3-phosphate~d Pmvak. @ 1997publishedby Elsevier ScienceLtd.
📜 SIMILAR VOLUMES
Optically pure 2-C-methyl-d-erythritol 4-phosphate, a key intermediate in the mevalonate-independent route for isoprenoid biosynthesis, is conveniently synthesized from 1,2-O-isopropylidene-a-d-xylofuranose, including the possibility of radiolabeling of this substrate.
In the bacterium Escherichia coli, gcpE is an essential gene in the methylerythritol phosphate pathway for isoprenoid biosynthesis. Incubation of [1-3 H]methylerythritol with an E. coli mutant defective in the gcpE gene resulted in the accumulation of [1-3 H]methylerythritol 2,4-cyclodiphosphate. Th