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还原亚硒酸盐产生红色单质硒光合细菌菌株的筛选与鉴定
引用本文:王东亮,肖敏,钱卫,韩波.还原亚硒酸盐产生红色单质硒光合细菌菌株的筛选与鉴定[J].微生物学报,2007,47(1):44-47.
作者姓名:王东亮  肖敏  钱卫  韩波
作者单位:山东大学微生物技术国家重点实验室,济南,250100
摘    要:从实验室保藏的光合细菌中筛选出一株对亚硒酸钠还原效率较高的菌株S3,其亚硒酸钠还原产物通过透射电子显微镜及EDX(Electron-Dispersive X-ray)分析确定为红色单质硒。菌株S3的形态学特征、生理生化特征及光合色素扫描结果与固氮红细菌(Rhodobacter azotoformans)的特征基本一致;16S rDNA序列(GenBank登录号为DQ402051)在系统发育树中与固氮红细菌同属一个类群,序列同源性为99%。根据上述结果将菌株S3鉴定为固氮红细菌。初步研究了该菌株还原亚硒酸钠的特性,首次报道固氮红细菌具有还原亚硒酸盐产生红色单质硒的能力,为今后利用微生物方法治理环境中硒污染、利用微生物方法获得活性红色单质硒以及对微生物还原亚硒酸盐产生红色单质硒的机理研究奠定了良好的基础。

关 键 词:光合细菌  红色单质硒  系统发育树  固氮红细菌
文章编号:0001-6209(2007)01-0044-04
收稿时间:2006/5/22 0:00:00
修稿时间:7/6/2006 12:00:00 AM

Screening and identification of a photosynthetic bacterium reducing selenite to red elemental selenium
WANG Dong-liang,XIAO Min,QIAN Wei and HAN Bo.Screening and identification of a photosynthetic bacterium reducing selenite to red elemental selenium[J].Acta Microbiologica Sinica,2007,47(1):44-47.
Authors:WANG Dong-liang  XIAO Min  QIAN Wei and HAN Bo
Institution:State Key Lab of Microbial Technology, Shandong University, Jinan 250100, China;State Key Lab of Microbial Technology, Shandong University, Jinan 250100, China;State Key Lab of Microbial Technology, Shandong University, Jinan 250100, China;State Key Lab of Microbial Technology, Shandong University, Jinan 250100, China
Abstract:Selenium is essential element for humans and animals but is very toxic at higher concentrations. In four inorganic states of selenate SeO4 2- ( VI)], selenite SeO3 2- (IV)], elemental selenium Se (0)] and selenide Se2- (- II )], selenite is well known to be more soluble and higher toxic than other three forms. Many microorganisms have the capacity to reduce selenite to red elemental selenium, which provide the potential to cope with the detoxification of pollution and to use the biological availability of red elemental selenium. Strain S3 that was more resistant to sodium selenite was selected from 20 photosynthetic bacteria preserved in laboratory. The red granule produced by S3 was identified as elemental selenium ( Se) by transmission electron microscopy and Electron-Dispersive X-ray (EDX) analysis. The granule diameter of the red elemental selenium was 5nm - 200nm, similar as the Nano-Se that has bioavailability. Morphology, physiology and photosynthetic pigments analysis results showed that strain S3 was essentially consistent with Rhodobacter azotoformans . The 16S rDNA sequence analysis (GenBank accession number DQ402051) suggested that strain S3 was clustered together with R. azotoformans in phylogenetic tree, with the sequence identity of 99% . Based on all the results of taxonomy, strain S3 was identified as R. azotoformans S3. The effects of selenite on growth kinetics and the ability to resistant selenite of strain S3 were investigated. In contrast to Rhodospirillum rubrum which was reported not to reduce selenite until the end of exponential growth, strain S3 transformed selenite (1.25mmol/L) at the beginning of the growth, suggesting that strain S3 and Rs. rubrum may employ different strategies to reduce selenite. Strain S3 can grow in the presence of up to 125mmol/L sodium selenite, which is much higher than those which could be resisted to by other bacteria such as Escherichia coli ( < 20mmol/L) and Ralstonia metallidurans CH34 ( < 6mmol/L) . It is firstly reported that R. azotoformans has the capacity to reduce selenite to red elemental selenium.
Keywords:16SrDNA
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