Institute of Marine and Coastal Sciences, Rutgers University, New Brunswick, NJ 08901, USA.
Department of Biochemistry and Microbiology, Rutgers University, New Brunswick, NJ 08901, USA.
Int J Syst Evol Microbiol. 2012 Dec;62(Pt 12):2921-2926. doi: 10.1099/ijs.0.039594-0. Epub 2012 Jan 20.
An aerobic, alkane-oxidizing bacterium, designated strain EPR92(T), was isolated from hydrothermal fluids that had been collected from a deep-sea vent on the East Pacific Rise (at 9° 50' N 104° 17' W). The cells of the novel strain were Gram-staining-negative rods that measured approximately 1.4 µm in length and 0.4 µm in width. Strain EPR92(T) grew at 20-40 °C (optimum 35 °C), with1.0-5.0% (w/v) NaCl (optimum 2.5%), and at pH 4.0-8.5 (optimum pH 7.5). The generation time under optimal conditions was 63 min. Strain EPR92(T) grew aerobically in artificial seawater minimal medium with n-alkanes as sole carbon and energy sources, and also in artificial seawater medium supplemented with peptone and yeast extract. The predominant fatty acids were C(18:1)ω7c, C(19:0) cyclo ω8c, 11-methyl C(18:1)ω7c and a putative C(12:0) aldehyde. The major polar lipids were phosphatidylglycerol, diphosphatidylglycerol, phosphatidylethanolamine, phosphatidylcholine and four unidentified aminolipids. The major respiratory quinone was Q-10 and the genomic DNA G+C content was 60.7 mol%. Phylogenetic analyses of the 16S rRNA gene showed that strain EPR92(T) belongs in the class Alphaproteobacteria and the recognized species that were most closely related to the novel strain were identified as Parvibaculum indicum P-31(T) (98.7% sequence similarity) and Parvibaculum lavamentivorans DS-1(T) (95.8%). In DNA-DNA hybridizations, the level of DNA-DNA relatedness observed between strain EPR92(T) and P. indicum P-31(T) was 47.7%, indicating that the two strains do not belong to the same species. Based on the phylogenetic, physiological, chemotaxonomic and genetic evidence, strain EPR92(T) represents a novel species within the genus Parvibaculum, for which the name Parvibaculum hydrocarboniclasticum sp. nov. is proposed. The type strain is EPR92(T) ( = DSM 23209 = JCM 16666(T)).
一株好氧、烷烃氧化细菌,命名为 EPR92(T) 菌株,从东太平洋洋脊深海喷口采集的热液中分离得到。该新菌株的细胞为革兰氏阴性杆状,长约 1.4 µm,宽约 0.4 µm。EPR92(T) 菌株在 20-40°C(最佳温度 35°C)、1.0-5.0%(w/v)NaCl(最佳 2.5%)和 pH4.0-8.5(最佳 pH7.5)下生长。在最佳条件下,代时为 63 分钟。EPR92(T) 菌株在含有烷烃作为唯一碳源和能源的人工海水基础培养基中好氧生长,也在含有蛋白胨和酵母提取物的人工海水中生长。优势脂肪酸为 C(18:1)ω7c、C(19:0)cyclo ω8c、11-甲基 C(18:1)ω7c 和一种假定的 C(12:0) 醛。主要极性脂为磷脂酰甘油、双磷脂酰甘油、磷脂酰乙醇胺、磷脂酰胆碱和四种未鉴定的胺脂。主要呼吸醌为 Q-10,基因组 DNA G+C 含量为 60.7 mol%。16S rRNA 基因的系统发育分析表明,EPR92(T) 菌株属于α变形菌纲,与新菌株最密切相关的公认种为 Parvibaculum indicum P-31(T)(98.7%序列相似性)和 Parvibaculum lavamentivorans DS-1(T)(95.8%)。在 DNA-DNA 杂交中,EPR92(T) 菌株与 P.indicum P-31(T) 之间观察到的 DNA-DNA 同源性水平为 47.7%,表明这两个菌株不属于同一物种。基于系统发育、生理、化学分类和遗传证据,EPR92(T) 菌株代表 Parvibaculum 属中的一个新种,建议将其命名为 Parvibaculum hydrocarboniclasticum sp. nov.。模式菌株为 EPR92(T)(=DSM 23209=JCM 16666(T))。