Jiang Sheng-Fang, Zhang Chu-Yi, Lao Xuan-Wen, Jia Wei-Chao, Yang Tao-Tao, Zhang Si-Yu, Xie Ying-Ying, Ye Pei-Zhe, Lan Rui, Lai Zi-Xiang, Yang Qiang, Huang Li-Nan
School of Life Sciences, Sun Yat-Sen University, Guangzhou, 510275, People's Republic of China.
Power China Northwest Engineering Corporation Limited, Xi'an, 710065, People's Republic of China.
Antonie Van Leeuwenhoek. 2025 Aug 28;118(10):142. doi: 10.1007/s10482-025-02152-2.
An anaerobic, Gram-stain-positive and spore-forming acidophilic sulfate-reducing bacterium, designated as SYSU MS00001, was isolated from acidic sediments of Zhongshan Iron Mine, P.R. China. The strain was straight-rod-shaped and motile, oxidase-negative and catalase-negative, with circular, convex, regular-edged and black-pigmented colonies (1-3 mm in diameter) on the solid basal salts/yeast extract plate. Growth and proliferation occurred at 10-40 °C (optimal: 30 °C), pH 3.5-7.5 (optimal: 5.0-5.5) and NaCl concentration of 0-1.6% (optimal: 0.2%), with a doubling time of 8.2 h under the optimal conditions. The strain utilised H/CO, organic acids (fumarate, citrate, pyruvate, malate, acetate, propionate, lactate, butyrate), alcohols (glycerol), and sugars (fructose, glucose, xylose) as electron donors for sulfate reduction. Sulfate, sulfur, sulfite, thiosulfate, fumarate and nitrate were used as electron acceptors in the presence of glycerol. It also fermented ethanol and methanol without sulfate. The main polar lipids were diphosphatidylglycerol, phosphatidylglycerol, phosphatidylethanolamine, unidentified phospholipids, unidentified aminophospholipid, unidentified lipids and unidentified glycolipids. The major fatty acids (> 5%) were C, C and summed features 3 (Cω7c/Cω6c). The respiratory quinones identified were MK-7 and MK-8(H). Phylogenetic analyses based on 16S rRNA gene and genome sequences indicated that the isolated strain should be assigned to the genus Desulfosporosinus, and the 16S rRNA gene sequence was most closely related to Desulfosporosinus acididurans M1 with similarity of 98.34%. The genomic DNA G + C content of SYSU MS00001 was 41.7%. The digital DNA-DNA hybridization (dDDH) and average nucleotide identity (ANI) values between SYSU MS00001 and D. acididurans M1 were 50.6% and 90.95%, respectively. On the basis of phenotypic, phylogenetic and genetic characteristics, strain SYSU MS00001 represents a novel species within the genus Desulfosporosinus, for which the name Desulfosporosinus sediminicola sp. nov. is proposed. The type strain is SYSU MS00001 (= GDMCC 1.4736 = KCTC 25900).
从中国广东省大宝山铁矿区的酸性沉积物中分离出一株厌氧、革兰氏阳性、产芽孢的嗜酸硫酸盐还原菌,命名为SYSU MS00001。该菌株为直杆状,具运动性,氧化酶阴性,过氧化氢酶阴性,在固体基础盐/酵母提取物平板上形成圆形、凸起、边缘规则且呈黑色的菌落(直径1-3毫米)。在10-40°C(最适温度30°C)、pH 3.5-7.5(最适pH 5.0-5.5)和NaCl浓度0-1.6%(最适浓度0.2%)的条件下生长繁殖,最适条件下的倍增时间为8.2小时。该菌株利用H/CO、有机酸(富马酸、柠檬酸、丙酮酸、苹果酸、乙酸、丙酸、乳酸、丁酸)、醇类(甘油)和糖类(果糖、葡萄糖、木糖)作为电子供体进行硫酸盐还原。在甘油存在的情况下,以硫酸盐、硫、亚硫酸盐、硫代硫酸盐、富马酸和硝酸盐作为电子受体。它也能在无硫酸盐的情况下发酵乙醇和甲醇。主要极性脂为双磷脂酰甘油、磷脂酰甘油、磷脂酰乙醇胺、未鉴定的磷脂、未鉴定的氨基磷脂、未鉴定的脂类和未鉴定的糖脂。主要脂肪酸(>5%)为C、C和总和特征3(Cω7c/Cω6c)。鉴定出的呼吸醌为MK-7和MK-8(H)。基于16S rRNA基因和基因组序列的系统发育分析表明,分离出的菌株应归入脱硫孢菌属,其16S rRNA基因序列与嗜酸脱硫孢菌M1的相似度最高,为98.34%。SYSU MS00001的基因组DNA G+C含量为41.7%。SYSU MS00001与嗜酸脱硫孢菌M1之间的数字DNA-DNA杂交(dDDH)值和平均核苷酸同一性(ANI)值分别为50.6%和90.95%。基于表型、系统发育和遗传特征,菌株SYSU MS00001代表脱硫孢菌属内的一个新物种,为此提出新物种名称嗜酸脱硫孢菌Desulfosporosinus sediminicola sp. nov.。模式菌株为SYSU MS00001(=GDMCC 1.4736 =KCTC 25900)。