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Applied and Environmental Microbiology, February 2006, p. 1079-1085, Vol. 72, No. 2
0099-2240/06/$08.00+0 doi:10.1128/AEM.72.2.1079-1085.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Molly C. Redmond,2 and
David L. Valentine3*
Marine Biology Research Division, Scripps Institution of Oceanography, and Department of Chemistry and Biochemistry, University of California, San Diego,1 Graduate Program in Marine Science, University of California, Santa Barbara,2 Department of Earth Science and Marine Science Institute, University of California, Santa Barbara, California3
Received 12 August 2005/ Accepted 8 November 2005
We used an H2-purging culture vessel to replace an H2-consuming syntrophic partner, allowing the growth of pure cultures of Syntrophothermus lipocalidus on butyrate and Aminobacterium colombiense on alanine. By decoupling the syntrophic association, it was possible to manipulate and monitor the single organism's growth environment and determine the change in Gibbs free energy yield (
G) in response to changes in the concentrations of reactants and products, the purging rate, and the temperature. In each of these situations, H2 production changed such that
G remained nearly constant for each organism (11.1 ± 1.4 kJ mol butyrate1 for S. lipocalidus and 58.2 ± 1.0 kJ mol alanine1 for A. colombiense). The cellular maintenance energy, determined from the
G value and the hydrogen production rate at the point where the cell number was constant, was 4.6 x 1013 kJ cell1 day1 for S. lipocalidus at 55°C and 6.2 x 1013 kJ cell1 day1 for A. colombiense at 37°C. S. lipocalidus, in particular, seems adapted to thrive under conditions of low energy availability.
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