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厌氧生境体系中产氢产乙酸细菌的FISH定量解析
引用本文:李艳娜,许科伟,堵国成,陈坚,刘和.厌氧生境体系中产氢产乙酸细菌的FISH定量解析[J].微生物学报,2007,47(6):1038-1043.
作者姓名:李艳娜  许科伟  堵国成  陈坚  刘和
作者单位:1. 江南大学生物工程学院环境生物技术研究室,无锡,214122
2. 江南大学生物工程学院环境生物技术研究室,无锡,214122;江南大学生物工程学院工业生物技术教育部重点实验室,无锡,214122
基金项目:国家自然科学基金;国家高技术研究发展计划(863计划)
摘    要:产氢产乙酸细菌是一类在有机物厌氧降解过程中起重要作用的细菌。以基于16S rRNA序列设计的特异性寡核苷酸探针为基础,优化FISH实验条件,确定该技术检测产氢产乙酸细菌的实验条件为样品固定19h、乙醇脱水5min,杂交缓冲液中甲酰胺浓度55%。运用建立的FISH技术检测了几种厌氧消化体系中产氢产乙酸细菌的数量,并与用传统MPN方法的结果进行了比较。结果表明,产氢产乙酸细菌分布广泛,废水处理UASB反应器和动物消化道,特别是反刍动物瘤胃中的产氢产乙酸细菌数量较高,其丰度分别为1.70×109 cells/mL样品,6.50×108 cells/mL样品。湖底沉积物中产氢产乙酸细菌数量较少,仅占整个微生物群落的0.4%,含量为1.20×108 cells/mL样品。

关 键 词:产氢产乙酸细菌  荧光原位杂交  寡核苷酸探针  厌氧体系
文章编号:0001-6209(2007)06-1038-06
收稿时间:7/3/2007 12:00:00 AM
修稿时间:9/7/2007 12:00:00 AM

Quantitative use of fluorescence in situ hybridization to detect syntrophic acetogenic bacteria in anaerobic environmental samples
LI Yan-n,XU Ke-wei,DU Guo-cheng,CHEN Jian and LIU He.Quantitative use of fluorescence in situ hybridization to detect syntrophic acetogenic bacteria in anaerobic environmental samples[J].Acta Microbiologica Sinica,2007,47(6):1038-1043.
Authors:LI Yan-n  XU Ke-wei  DU Guo-cheng  CHEN Jian and LIU He
Institution:Laboratory of Environmental Biotechnology; School of Biotechnology; Jiangnan University; Wuxi 214122; China;Laboratory of Environmental Biotechnology; School of Biotechnology; Jiangnan University; Wuxi 214122; China;1.Laboratory of Environmental Biotechnology; School of Biotechnology; Jiangnan University; Wuxi 214122; China;2.Key Laboratory of Industrial Biotechnology; Ministry of Education; China;1.Laboratory of Environmental Biotechnology; School of Biotechnology; Jiangnan University; Wuxi 214122; China;2.Key Laboratory of Industrial Biotechnology; Ministry of Education; China;Laboratory of Environmental Biotechnology; School of Biotechnology; Jiangnan University; Wuxi 214122; China
Abstract:Syntrophic acetogenic bacteria, an important functional one in anaerobic habitats, were detected and counted by fluorescence in situ hybridization (FISH) technology by using 16S rRNA-based oligonucleotide probes. For enumeration and quantification of the targeted bacteria, an attempt was made to optimize the hybridization conditions. The optimum conditions are as follows: a fixation time of 19h, a dehydrated time of 5 min, and a formamide concentration of 55% in hybridized solution. The abundance of syntrophic acetogenic bacteria of different environmental samples were quantified by FISH and the results showed that Upflow Anaerobic Sludge Reactor (UASB) treating STHZ high-concentration organic wastewater and the digestive tract of some animals were the main habitats of syntrophic acetogenic bacteria. The numbers of syntrophic acetogenic bacteria in UASB and cattle manure were 1.70 x 10(9) cells/mL sample and 6.50 x 10(8) cells/mL sample, respectively. Meanwhile, the sediments of rivers and lakes existed less of the bacteria and the contents of them were just about 1.20 x 10(8) cells/mL sample in Taihu lake.
Keywords:syntrophic acetogenic bacteria  fluorescence in situ hybridization  oligonucleotide probes  anaerobic system
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