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一株硫酸盐还原菌的分离鉴定和系统发育分析
引用本文:李建军,叶广运,陈进林,孙国萍,梁世中.一株硫酸盐还原菌的分离鉴定和系统发育分析[J].微生物学通报,2009,36(10):1476-1482.
作者姓名:李建军  叶广运  陈进林  孙国萍  梁世中
作者单位:1. 华南理工大学,广东,广州,510006;广东省微生物研究所,广东,广州,510070;广东省微生物应用新技术公共实验室,广东,广州,510070
2. 广东省微生物研究所,广东,广州,510070;广东省微生物应用新技术公共实验室,广东,广州,510070
3. 华南理工大学,广东,广州,510006
基金项目:国家863计划项目(No. 2006AA06Z322); 广州市项目(No. 2008C13G041); 广东省项目(No. 2008B040200015)
摘    要:从处理硫酸盐废水的厌氧折流板反应器中分离得到一株硫酸盐还原菌D11, 该菌株革兰氏反应阴性, 无芽孢, 菌体杆状稍有弯曲, 宽度在0.6 μm~0.8 μm, 长度在1.8 μm~3.3 μm之间, 有极生单鞭毛, 能运动, 接触酶阳性, 氧化酶阴性。菌株生长的pH范围介于6.0~8.0之间, 最适pH为7.0, 生长温度范围为25°C~37°C, 最适温度为30°C。能够以葡萄糖、蔗糖、乙酸、乳酸、乙醇和丙二醇为唯一碳源生长, 不能利用丙三醇、丁醇、琥珀酸和苹果酸。菌株DNA的G+C含量为62.7 mo

关 键 词:硫酸盐还原菌    16S  rRNA    DSR

Isolation, Identification of a Sulfate Reducing Bacteria D11 and Its Phylogenetic Analysis
LI Jian-Jun,YE Guang-Yun,CHEN Jin-Lin,SUN Guo-Ping and LIANG Shi-Zhong.Isolation, Identification of a Sulfate Reducing Bacteria D11 and Its Phylogenetic Analysis[J].Microbiology,2009,36(10):1476-1482.
Authors:LI Jian-Jun  YE Guang-Yun  CHEN Jin-Lin  SUN Guo-Ping and LIANG Shi-Zhong
Institution:South China University of Technology, Guangzhou, Guangdong 510006, China; Guangdong Institute of Microbiology, Guangzhou, Guangdong 510070, China; Guangdong Provincial Key Laboratory of Microbial Culture Collection and Application, Guangzhou, Guangdong 51;Guangdong Institute of Microbiology, Guangzhou, Guangdong 510070, China; Guangdong Provincial Key Laboratory of Microbial Culture Collection and Application, Guangzhou, Guangdong 510070, China;Guangdong Institute of Microbiology, Guangzhou, Guangdong 510070, China; Guangdong Provincial Key Laboratory of Microbial Culture Collection and Application, Guangzhou, Guangdong 510070, China;Guangdong Institute of Microbiology, Guangzhou, Guangdong 510070, China; Guangdong Provincial Key Laboratory of Microbial Culture Collection and Application, Guangzhou, Guangdong 510070, China;South China University of Technology, Guangzhou, Guangdong 510006, China
Abstract:A sulfate-reducing bacteria strain, designated D11, was isolated from an anaerobic baffled reactor treating waste water containing sulfate. The cells of strain D11 were found to be Gram-negative, non-spore-forming, slightly curved rods, 0.6 μm~0.8 μm wide and 1.8 μm~3.3 μm long, motile by a single polar flagellum, catalase positive and oxidase negative. The pH range for growth was 6.0~8.0 (optimum pH 7.0) and the temperature range for was 25℃~37℃(optimum 30℃). Strain D11 can use glucose, fructose, acetate, lactate, alcohol and propanediol as sole carbon source for growth and did not use glycerol, butanol, succinate and malate. The G+C content of the DNA was 62.7 mol%. Phylogenetic analysis based on 16S rRNA and DSR gene sequence showed strain D11 was closely related to the type strain of Desulfovibrio vulgaris Hildenborough and Desulfovibrio vulgaris DP4 (99% sequence similarity).
Keywords:Sulfate reducing bacteria  16S rRNA  DSR
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