The deep-subsurface sulfate reducer Desulfotomaculum kuznetsovii employs two methanol-degrading pathways
Diana Z. Sousa (Wageningen University & Research)
M. Visser (Wageningen University & Research)
Antonie H. Van Gelder (Wageningen University & Research)
Sjef Boeren (Wageningen University & Research)
MM Pieterse (TU Delft - OLD BT/Analytical Biotechnology, Netherlands Proteomics Centre)
M.W.H. Pinkse (TU Delft - OLD BT/Analytical Biotechnology, Netherlands Proteomics Centre)
P.D.E.M. Verhaert (Maastricht University, Netherlands Proteomics Centre, Janssen Pharmaceutica Campus, TU Delft - BT/Afdelingsbureau)
Carsten Vogt (Helmholtz Centre for Environmental Research - UFZ)
Steffi Franke (Helmholtz Centre for Environmental Research - UFZ)
Steffen Kümmel (Helmholtz Centre for Environmental Research - UFZ)
Alfons J M Stams (University of Minho, Wageningen University & Research)
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Abstract
Methanol is generally metabolized through a pathway initiated by a cobalamine-containing methanol methyltransferase by anaerobic methylotrophs (such as methanogens and acetogens), or through oxidation to formaldehyde using a methanol dehydrogenase by aerobes. Methanol is an important substrate in deep-subsurface environments, where thermophilic sulfate-reducing bacteria of the genus Desulfotomaculum have key roles. Here, we study the methanol metabolism of Desulfotomaculum kuznetsovii strain 17T, isolated from a 3000-m deep geothermal water reservoir. We use proteomics to analyze cells grown with methanol and sulfate in the presence and absence of cobalt and vitamin B12. The results indicate the presence of two methanol-degrading pathways in D. kuznetsovii, a cobalt-dependent methanol methyltransferase and a cobalt-independent methanol dehydrogenase, which is further confirmed by stable isotope fractionation. This is the first report of a microorganism utilizing two distinct methanol conversion pathways. We hypothesize that this gives D. kuznetsovii a competitive advantage in its natural environment.