Re-citrate synthase from Clostridium kluyveri is phylogenetically related to homocitrate synthase and isopropylmalate synthase rather than to Si-citrate synthase

2007 | journal article. A publication with affiliation to the University of Göttingen.

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​Re-citrate synthase from Clostridium kluyveri is phylogenetically related to homocitrate synthase and isopropylmalate synthase rather than to Si-citrate synthase​
Li, F.; Hagemeier, C. H.; Seedorf, H.; Gottschalk, G. & Thauer, R. K.​ (2007) 
Journal of Bacteriology189(11) pp. 4299​-4304​.​ DOI: https://doi.org/10.1128/JB.00198-07 

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Authors
Li, Fuli; Hagemeier, Christoph H.; Seedorf, Henning; Gottschalk, Gerhard; Thauer, Rudolf K.
Abstract
The synthesis of citrate from acetyl-coenzyme A and oxaloacetate is catalyzed in most organisms by a Si-citrate synthase, which is Si-face stereospecific with respect to C-2 of oxaloacetate. However, in Clostridium kluyveri and some other strictly anaerobic bacteria, the reaction is catalyzed by a Re-citrate synthase, whose primary structure has remained elusive. We report here that Re-citrate synthase from C. kluyveri is the product of a gene predicted to encode isopropylmalate synthase. C. kluyveri is also shown to contain a gene for Si-citrate synthase, which explains why cell extracts of the organism always exhibit some Si-citrate synthase activity.
Issue Date
2007
Status
published
Publisher
Amer Soc Microbiology
Journal
Journal of Bacteriology 
ISSN
1098-5530; 0021-9193

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