Imachi Hiroyuki, Sekiguchi Yuji, Kamagata Yoichi, Loy Alexander, Qiu Yan-Ling, Hugenholtz Philip, Kimura Nobutada, Wagner Michael, Ohashi Akiyoshi, Harada Hideki
Department of Environmental Systems Engineering, Nagaoka University of Technology, 1603-1 Kamitomioka, Nagaoka, Niigata 940-2188, Japan.
Appl Environ Microbiol. 2006 Mar;72(3):2080-91. doi: 10.1128/AEM.72.3.2080-2091.2006.
The classical perception of members of the gram-positive Desulfotomaculum cluster I as sulfate-reducing bacteria was recently challenged by the isolation of new representatives lacking the ability for anaerobic sulfate respiration. For example, the two described syntrophic propionate-oxidizing species of the genus Pelotomaculum form the novel Desulfotomaculum subcluster Ih. In the present study, we applied a polyphasic approach by using cultivation-independent and culturing techniques in order to further characterize the occurrence, abundance, and physiological properties of subcluster Ih bacteria in low-sulfate, methanogenic environments. 16S rRNA (gene)-based cloning, quantitative fluorescence in situ hybridization, and real-time PCR analyses showed that the subcluster Ih population composed a considerable part of the Desulfotomaculum cluster I community in almost all samples examined. Additionally, five propionate-degrading syntrophic enrichments of subcluster Ih bacteria were successfully established, from one of which the new strain MGP was isolated in coculture with a hydrogenotrophic methanogen. None of the cultures analyzed, including previously described Pelotomaculum species and strain MGP, consumed sulfite, sulfate, or organosulfonates. In accordance with these phenotypic observations, a PCR-based screening for dsrAB (key genes of the sulfate respiration pathway encoding the alpha and beta subunits of the dissimilatory sulfite reductase) of all enrichments/(co)cultures was negative with one exception. Surprisingly, strain MGP contained dsrAB, which were transcribed in the presence and absence of sulfate. Based on these and previous findings, we hypothesize that members of Desulfotomaculum subcluster Ih have recently adopted a syntrophic lifestyle to thrive in low-sulfate, methanogenic environments and thus have lost their ancestral ability for dissimilatory sulfate/sulfite reduction.
革兰氏阳性脱硫肠状菌属第一簇成员作为硫酸盐还原菌的传统认知,最近受到了新分离出的缺乏厌氧硫酸盐呼吸能力的代表菌株的挑战。例如,已描述的两个互营丙酸氧化型泥杆菌属物种形成了新的脱硫肠状菌属亚簇Ih。在本研究中,我们采用了多相方法,运用非培养和培养技术,以进一步表征亚簇Ih细菌在低硫酸盐、产甲烷环境中的出现情况、丰度和生理特性。基于16S rRNA(基因)的克隆、定量荧光原位杂交和实时PCR分析表明,在几乎所有检测的样本中,亚簇Ih菌群在脱硫肠状菌属第一簇群落中占相当大的比例。此外,成功建立了5个亚簇Ih细菌的丙酸降解互营富集培养物,其中一个与氢营养型产甲烷菌共培养分离出了新菌株MGP。所分析的培养物,包括先前描述的泥杆菌属物种和菌株MGP,均未消耗亚硫酸盐、硫酸盐或有机磺酸盐。与这些表型观察结果一致,对所有富集培养物/(共)培养物进行基于PCR的dsrAB(编码异化亚硫酸盐还原酶α和β亚基的硫酸盐呼吸途径关键基因)筛选,除一个例外均为阴性。令人惊讶的是,菌株MGP含有dsrAB,且在有硫酸盐和无硫酸盐的情况下均有转录。基于这些及先前的发现,我们推测脱硫肠状菌属亚簇Ih的成员最近采用了互营生活方式,以便在低硫酸盐、产甲烷环境中繁衍,因此丧失了其祖先异化硫酸盐/亚硫酸盐还原的能力。