Kuhner C H, Frank C, Griesshammer A, Schmittroth M, Acker G, Gössner A, Drake H L
Lehrstuhl für Okologische Mikrobiologie, BITOK, Bayreuth, Germany.
Int J Syst Bacteriol. 1997 Apr;47(2):352-8. doi: 10.1099/00207713-47-2-352.
Sporomusa silvacetica sp. nov. DG-1T (= DSMZ 10669T) (T = type strain) was isolated from well-drained, aggregated forest soil (pH 6.0) in east-central Germany. The cells were obligately anaerobic, slightly curved rods and were motile by means of laterally inserted flagella on the concave side of each cell. Typical cells were approximately 3.5 by 0.7 micron. Cells stained weakly gram positive, but thin sections revealed a complex multilayer cell wall. Spores were spherical and distended the sporangia. Growth and substrate utilization occurred with ferulate, vanillate, fructose, betaine, fumarate, 2,3-butanediol, pyruvate, lactate, glycerol, ethanol, methanol, formate, and H2-CO2. With most substrates, acetate was the primary reduced end product and was produced in stoichiometries indicative of an acetyl-coenzyme A pathway-dependent metabolism. Fumarate was dismutated to succinate and acetate. Methoxyl and acrylate groups of various aromatic compounds were O-demethylated and reduced, respectively. Yeast extract was not required for growth. Cells grew optimally at approximately 30 degrees C and pH 6.8; under these conditions and with fructose as the substrate, the doubling time was approximately 14 h. The lowest temperature that supported growth was between 5 and 10 degrees C. The carbon monoxide dehydrogenase and hydrogenase activities were approximately 9 and 102 mumol min-1 mg of protein-1, respectively. A type b cytochrome was detected in the membrane. The G + C content was approximately 43 mol%. Phylogenetic analysis of the 16S ribosomal DNA indicated that DG-1T was most closely related to members of the genus Sporomusa in the Clostridium subphylum of the gram-positive bacteria.
森林土壤梭菌新种Sporomusa silvacetica sp. nov. DG-1T(= DSMZ 10669T)(T = 模式菌株)从德国中东部排水良好的团聚森林土壤(pH 6.0)中分离得到。细胞为专性厌氧,呈微弯杆状,通过每个细胞凹面侧向插入的鞭毛运动。典型细胞大小约为3.5×0.7微米。细胞革兰氏阳性染色较弱,但超薄切片显示有复杂的多层细胞壁。孢子呈球形,使孢子囊膨胀。在阿魏酸、香草酸、果糖、甜菜碱、富马酸、2,3 - 丁二醇、丙酮酸、乳酸、甘油、乙醇、甲醇、甲酸和H2 - CO2存在的情况下生长并利用底物。对于大多数底物,乙酸盐是主要的还原终产物,其产生的化学计量表明依赖于乙酰辅酶A途径的代谢。富马酸歧化为琥珀酸和乙酸盐。各种芳香族化合物的甲氧基和丙烯酸酯基团分别进行O - 去甲基化和还原反应。生长不需要酵母提取物。细胞在约30℃和pH 6.8时生长最佳;在这些条件下以果糖为底物时,倍增时间约为14小时。支持生长的最低温度在5至10℃之间。一氧化碳脱氢酶和氢化酶活性分别约为9和102 μmol min-1 mg蛋白质-1。在膜中检测到b型细胞色素。G + C含量约为43 mol%。16S核糖体DNA的系统发育分析表明,DG-1T与革兰氏阳性菌梭菌亚门梭菌属的成员关系最为密切。