Desulfomusa hansenii gen. nov., sp. nov., a novel marine propionate-degrading, sulfate-reducing bacterium isolated from Zostera marina roots

K Finster, TR Thomsen and NB Ramsing Department of Microbial Ecology, Institute of Biological Sciences, University of Aarhus, 8000 Aarhus, Denmark The physiology and phylogeny of a novel sulfate-reducing bacterium, isolated from surface-sterilized roots of the marine macrophyte Zostera marina, are presented. The strain, designated P1(T), was enriched and isolated in defined oxygen-free, bicarbonate-buffered, iron-reduced seawater medium with propionate as sole carbon source and electron donor and sulfate as electron acceptor. Strain P1(T) had a rod-shaped, slightly curved cell morphology and was motile by means of a single polar flagellum. Cells generally aggregated in clumps throughout the growth phase. High CaCl(2) (10 mM) and MgCl(2) (50 mM) concentrations were required for optimum growth. In addition to propionate, strain P1(T) utilized fumarate, succinate, pyruvate, ethanol, butanol and alanine. Oxidation of propionate was incomplete and acetate was formed in stoichiometric amounts. Strain P1(T) thus resembles members of the sulfate-reducing genera Desulfobulbus and Desulforhopalus, which both oxidize propionate incompletely and form acetate in addition to CO(2). However, sequence analysis of the small-subunit rDNA and the dissimilatory sulfite reductase gene revealed that strain P1(T) was unrelated to the incomplete oxidizers Desulfobulbus and Desulforhopalus and that it constitutes a novel lineage affiliated with the genera Desulfococcus, Desulfosarcina, Desulfonema and 'Desulfobotulus'. Members of this branch, with the exception of 'Desulfobotulus sapovorans', oxidize a variety of substrates completely to CO(2). Strain P1(T) (=DSM 12642(T)=ATCC 700811(T)) is therefore proposed as Desulfomusa hansenii gen. nov., sp. nov. Strain P1(T) thus illustrates the difficulty of extrapolating rRNA similarities to physiology and/or ecological function.