Document Detail


Both forward and reverse TCA cycles operate in green sulfur bacteria.
MedLine Citation:
PMID:  20650900     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The anoxygenic green sulfur bacteria (GSBs) assimilate CO(2) autotrophically through the reductive (reverse) tricarboxylic acid (RTCA) cycle. Some organic carbon sources, such as acetate and pyruvate, can be assimilated during the phototrophic growth of the GSBs, in the presence of CO(2) or HCO(3)(-). It has not been established why the inorganic carbonis required for incorporating organic carbon for growth and how the organic carbons are assimilated. In this report, we probed carbon flux during autotrophic and mixotrophic growth of the GSB Chlorobaculum tepidum. Our data indicate the following: (a) the RTCA cycle is active during autotrophic and mixotrophic growth; (b) the flux from pyruvate to acetyl-CoA is very low and acetyl-CoA is synthesized through the RTCA cycle and acetate assimilation; (c) pyruvate is largely assimilated through the RTCA cycle; and (d) acetate can be assimilated via both of the RTCA as well as the oxidative (forward) TCA (OTCA) cycle. The OTCA cycle revealed herein may explain better cell growth during mixotrophic growth with acetate, as energy is generated through the OTCA cycle. Furthermore, the genes specific for the OTCA cycle are either absent or down-regulated during phototrophic growth, implying that the OTCA cycle is not complete, and CO(2) is required for the RTCA cycle to produce metabolites in the TCA cycle. Moreover, CO(2) is essential for assimilating acetate and pyruvate through the CO(2)-anaplerotic pathway and pyruvate synthesis from acetyl-CoA.
Authors:
Kuo-Hsiang Tang; Robert E Blankenship
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.     Date:  2010-07-22
Journal Detail:
Title:  The Journal of biological chemistry     Volume:  285     ISSN:  1083-351X     ISO Abbreviation:  J. Biol. Chem.     Publication Date:  2010 Nov 
Date Detail:
Created Date:  2010-11-08     Completed Date:  2011-02-09     Revised Date:  2011-11-14    
Medline Journal Info:
Nlm Unique ID:  2985121R     Medline TA:  J Biol Chem     Country:  United States    
Other Details:
Languages:  eng     Pagination:  35848-54     Citation Subset:  IM    
Affiliation:
Department of Biology and Chemistry, Washington University, St Louis, Missouri 63130, USA.
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MeSH Terms
Descriptor/Qualifier:
ATP Citrate (pro-S)-Lyase / genetics,  metabolism
Acetate Kinase / genetics,  metabolism
Acetates / chemistry,  metabolism
Acetyl Coenzyme A / chemistry,  metabolism
Autotrophic Processes
Bacterial Proteins / genetics,  metabolism*
Biomass
Carbon / metabolism
Carbon Isotopes
Chlorobi / genetics,  growth & development,  metabolism*
Citric Acid Cycle*
Coenzyme A Ligases / genetics,  metabolism
Gene Expression Regulation, Bacterial
Lactic Acid / chemistry,  metabolism
Metabolic Networks and Pathways
Models, Biological
Molecular Structure
Pyruvic Acid / chemistry,  metabolism
Reverse Transcriptase Polymerase Chain Reaction
Grant Support
ID/Acronym/Agency:
R01-GM57391/GM/NIGMS NIH HHS
Chemical
Reg. No./Substance:
0/Acetates; 0/Bacterial Proteins; 0/Carbon Isotopes; 127-17-3/Pyruvic Acid; 50-21-5/Lactic Acid; 72-89-9/Acetyl Coenzyme A; 7440-44-0/Carbon; EC 2.3.3.8/ATP Citrate (pro-S)-Lyase; EC 2.7.2.1/Acetate Kinase; EC 6.2.1.-/Coenzyme A Ligases; EC 6.2.1.13/acetate-CoA ligase (ADP-forming)

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