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Applied and Environmental Microbiology
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General Microbial Ecology

Radioassay for Hydrogenase Activity in Viable Cells and Documentation of Aerobic Hydrogen-Consuming Bacteria Living in Extreme Environments

Bernhard Schink, F. S. Lupton, J. G. Zeikus
Bernhard Schink
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F. S. Lupton
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J. G. Zeikus
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ABSTRACT

An isotopic tracer assay based on the hydrogenase-dependent formation of tritiated water from tritium gas was developed for in life analysis of microbial hydrogen transformation. This method allowed detection of bacterial hydrogen metabolism in pure cultures or in natural samples obtained from aquatic ecosystems. A differentiation between chemical-biological and aerobic-anaerobic hydrogen metabolism was established by variation of the experimental incubation temperature or by addition of selective inhibitors. Hydrogenase activity was shown to be proportional to the consumption or production of hydrogen by cultures of Desulfovibrio vulgaris, Clostridium pasteurianum, and Methanosarcina barkeri. This method was applied, in connection with measurements of free hydrogen and most-probable-number enumerations, in aerobic natural source waters to establish the activity and document the ecology of hydrogen-consuming bacteria in extreme acid, thermal, or saline environments. The utility of the assay is based in part on the ability to quantify bacterial hydrogen transformation at natural hydrogen partial pressures, without the use of artificial electron acceptors.

FOOTNOTES

  • ↵† Present address: Fakultat fur Biologie, Universitat Konstanz, Postfach 5560, D-7750 Konstanz, West Germany.

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Radioassay for Hydrogenase Activity in Viable Cells and Documentation of Aerobic Hydrogen-Consuming Bacteria Living in Extreme Environments
Bernhard Schink, F. S. Lupton, J. G. Zeikus
Applied and Environmental Microbiology May 1983, 45 (5) 1491-1500; DOI:

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Radioassay for Hydrogenase Activity in Viable Cells and Documentation of Aerobic Hydrogen-Consuming Bacteria Living in Extreme Environments
Bernhard Schink, F. S. Lupton, J. G. Zeikus
Applied and Environmental Microbiology May 1983, 45 (5) 1491-1500; DOI:
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