Desulfotignum phosphitoxidans sp. nov., a new marine sulfate reducer that oxidizes phosphite to phosphate
Open accessAbstract
A new sulfate-reducing bacterium was isolated from marine sediment with phosphite as sole electron donor and CO(2) as the only carbon source. Strain FiPS-3 grew slowly, with doubling times of 3-4 days, and oxidized phosphite, hydrogen, formate, acetate, fumarate, pyruvate, glycine, glutamate, and other substrates nearly completely, with concomitant reduction of sulfate to sulfide. Acetate was formed as a side product to a small extent. Glucose, arabinose, and proline were partly oxidized and partly fermented to acetate plus propionate. Growth with phosphite, hydrogen, or formate was autotrophic. Also, in the presence of sulfate, CO dehydrogenase was present, and added acetate did not increase growth rates or growth yields. In the absence of sulfate, phosphite oxidation was coupled to homoacetogenic acetate formation, with growth yields similar to those in the presence of sulfate. Cells were small rods, 0.6 - 0.8 x 2-4 microm in size, and gram-negative, with a G+C content of 53.9 mol%. They contained desulforubidin, but no desulfoviridin. Based on sequence analysis of the 16S rRNA gene and the sulfite reductase genes dsrAB, strain FiPS-3 was found to be closely related to Desulfotignum balticum. However, physiological properties differed in many points from those of D. balticum. These findings justify the establishment of a new species, Desulfotignum phosphitoxidans.
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The midpoint potential for the reduction of phosphate to phosphite is -690 mV at pH 7 and 25°C, and becomes more negative with higher pH.
“The midpoint potential for the reduction of phosphate to phosphite is –690 mV at pH 7 and 25°C (Schink et al., 2002) (see Figure 2) but becomes more negative with higher pH (Bernhard Schink pers. comm.).”
From Serpentinization as the source of energy, electrons, organics, catalysts, nutrients and pH gradients for the origin of LUCA and life (2023) · cites this paper as Schink et al., 2002
Phosphite is the only reductant other than H2 that is known to fuel chemolithoautotrophic growth using the acetyl-CoA pathway.
“It is the only reductant other than H2 that is known to fuel chemolithoautotrophic growth using the acetyl-CoA pathway.”
From Serpentinization as the source of energy, electrons, organics, catalysts, nutrients and pH gradients for the origin of LUCA and life (2023) · cites this paper as Schink et al., 2002
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Energy conservation in chemotrophic anaerobic bacteria
Thauer, R. K., Jungermann, K., & Decker, K. (1977) · Bacteriological Reviews · doi:10.1128/br.41.1.100-180.1977 · Cited by 4,146 · cited 2× · see citing works
“…2 O → ATP (ADP) + 2H + + 2e − E (physiol) = −432mV (3) the redox potential would be shifted to –432 mV if about 50 kJ would be spent in the formation of an energy-rich phosphoric acid anhydride linkage, taking the concentrations of ATP and ADP in the growing cell into account (Thauer et al. 1977).”
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Lever, M. A., Heuer, V. B., Morono, Y., Masui, N., Schmidt, F., Alperin, M. J., Inagaki, F., Hinrichs, K.-U., & Teske, A. (2010) · Geomicrobiology Journal · doi:10.1080/01490450903456681 · Cited by 86 · see citing works
Schwander, L., Brabender, M., Mrnjavac, N., Wimmer, J. L. E., Preiner, M., & Martin, W. F. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1257597 · Cited by 65 · see citing works
“In the absence of sulfate, its metabolism was that of an acetogen with energy generated by CO 2 reduction to acetate but using phosphite instead of H 2 as a source of electrons (Schink et al., 2002).”
BackgroundInfluentialThe metabolic network of the last bacterial common ancestor
Xavier, J. C., Gerhards, R. E., Wimmer, J. L. E., Brueckner, J., Tria, F. D. K., & Martin, W. F. (2021) · Communications Biology · doi:10.1038/s42003-021-01918-4 · Cited by 59 · see citing works
The diversity and evolution of microbial dissimilatory phosphite oxidation
Ewens, S. D., Gomberg, A. F. S., Barnum, T. P., Borton, M. A., Carlson, H. K., Wrighton, K. C., & Coates, J. D. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2020024118 · Cited by 48 · see citing works
- Authors
- Schink, B., Thiemann, V., Laue, H., & Friedrich, M.
- Affiliations
- University of Konstanz (DE)
- Max Planck Institute for Terrestrial Microbiology (DE)
- Venue
- Archives of Microbiology
- Published
- 2002-05-01
- Volume
- 177
- Issue
- 5
- Pages
- 381-391
- ISSN
- 0003-9276 (ISSN-L)
- 0302-8933
- 1432-072X
- OpenAlex
- W2168385167
- Cited by
- 116
- References
- 1
- Citations by year
- 2026: 6 · 2025: 4 · 2024: 4 · 2023: 12 · 2022: 3 · 2021: 8 · 2020: 8 · 2019: 4 · 2018: 3 · 2017: 1 · 2016: 3 · 2015: 4 · 2014: 9 · 2013: 8 · 2012: 2
- FWCI
- 5.66
- Type
- journal article
- Language
- en
- Open access
- green
- nbn-resolving.de
- Licence
- cc-by-nc-nd
- www.springer.com/tdm (tdm)
- Locations
- Archives of Microbiology (publishedVersion)
- PubMed (publishedVersion)
- KOPS (University of Konstanz) (submittedVersion, cc-by-nc-nd)
- Max Planck Institute for Plasma Physics (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Funders
- Max-Planck-Gesellschaft
- Universität Konstanz
- Topics
- Physical Sciences › Environmental Science › Ecology › Microbial Community Ecology and Physiology
- Physical Sciences › Environmental Science › Environmental Chemistry › Methane Hydrates and Related Phenomena
- Physical Sciences › Environmental Science › Environmental Engineering › Microbial Fuel Cells and Bioremediation
- Keywords
- novel bacterial species, sulfate-reducing bacteria, phosphite oxidation, phosphate formation, marine sediment bacteria, homoacetogenesis, autotrophic growth, 16S rRNA phylogeny
- MeSH terms
- Anaerobiosis, Base Composition, Cell Division, DNA, Ribosomal, Genes, Bacterial, Gram-Negative Anaerobic Bacteria, Phylogeny, Pigments, Biological, RNA, Ribosomal, 16S, Sulfates, Phosphites, Geologic Sediments
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