AEM
Home Help [Feedback] [For Subscribers] [Archive] [Search] --
AEM Accepts, published online ahead of print on 3 November 2006
This Article
Right arrow Full Text (PDF)
Right arrow Other Versions of this Article:
AEM.01415-06v1
73/1/64    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hong, Y.
Right arrow Articles by Sun, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hong, Y.
Right arrow Articles by Sun, G.
Agricola
Right arrow Articles by Hong, Y.
Right arrow Articles by Sun, G.

 Previous Article  |  Next Article 

Appl. Environ. Microbiol. doi:10.1128/AEM.01415-06
Copyright (c) 2006, American Society for Microbiology and/or the Listed Authors/Institutions. All Rights Reserved.

Respiration and Growth of Shewanella decolorationis S12 with Azo Compound as Sole Electron Acceptor

Yiguo Hong, Meiying Xu, Jun Guo, Zhicheng Xu, Xingjuan Chen, and Guoping Sun*

Guangdong Provincial Key Laboratory of Microbial Culture Collection and Application, Guangdong Institute of Microbiology, Guangzhou 510070, China; South China Institute of Botany, Chinese Academy of Science, Guangzhou 510650, China; Graduate School of the Chinese Academy of Sciences, Beijing 100039, China

* To whom correspondence should be addressed. Email: guopingsun{at}163.com.


   Abstract

The ability of Shewanella decolorationis S12 to obtain energy for growth by coupling the oxidation of various electron donors to dissimilatory azoreduction was investigated. This microorganism can reduce a variety of azo dyes using formate, lactate, pyruvate or HB2B as the electron donor. Furthermore, strain S12 grew to a maximal density of 3.0x107 cells per ml after compete reduction of 2.0 mM amaranth in a defined medium. This was accompanied by a stoichiometric consumption of 4.0 mM formate over time when amaranth and formate were supplied as sole electron acceptor and donor, respectively, suggesting that microbial azoreduction is an electron transport process, and that this electron transport can yield energy to support growth. Purified membranous, periplasmic and cytoplasmic fractions from S12 were analyzed, but only the membranous fraction was capable of reducing azo dyes with formate, lactate, pyruvate or HB2B as the electron donor. The presence of 5 µM Cu2+ ions, 200 µM dicumarol, 100 µM stigmatellin and 100 µM metyrapone inhibited anaerobic azoreduction activity by both whole cells and the purified membrane fraction, showing that dehydrogenases, cytochromes and menaquinone are essential electron transfer components for azoreduction. These results provide evidence that the microbial anaerobic azoreduction is linked to the electron transport chain and suggest that the dissimilatory azoreduction is a form of microbial anaerobic respiration. These findings not only expand the number of potential electron acceptors known for microbial energy conservation, but also elucidate the mechanisms of microbial anaerobic azoreduction.







Home Help [Feedback] [For Subscribers] [Archive] [Search] --
J. Bacteriol. Microbiol. Mol. Biol. Rev. Eukaryot. Cell All ASM Journals

Copyright © 2006 by the American Society for Microbiology. All rights reserved.