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通过根际中0.45微米孔径过滤器的细菌的系统发育分析。

Phylogenic analysis of bacteria passed through 0.45-microm-pore-size filters in the rhizosphere.

作者信息

Tabei Yosuke, Ueno Kohji

机构信息

The Laboratory of Microbiology, Faculty of Pharmacy, Research Institute for Pharmaceutical Sciences, Graduate School of Pharmaceutical Sciences, Musashino University, 1-1-20 Shinmachi, Nishitokyo, Tokyo, Japan.

出版信息

J Gen Appl Microbiol. 2010 Apr;56(2):129-36. doi: 10.2323/jgam.56.129.

Abstract

Molecular analyses of 16S ribosomal RNA genes (rDNA) revealed that microbial communities in the rhizosphere are highly complex. To systematically characterize the cell size of the bacteria in the rhizosphere, we selected bacteria that potentially could be passed through 0.22- or 0.45-microm-pore-size filters and then PCR amplified the 16S rDNA genes using the universal primer pairs 27F/1492R and 63F/1387R. The PCR-amplified rDNAs extracted from bacteria that had been passed through 0.45-microm-pore-size filters could be detected in agarose gels after electrophoresis; whereas after filtration of the bacteria through 0.22-microm-pore-size filters no PCR-amplified rDNAs were found. Comparison of random cloning and sequencing of the libraries of the PCR-amplified rDNAs with or without cell size selection showed that bacteria belonging to the candidate phylogenic divisions of OD1 (OP11-derived 1), OP11, TM7, and OP5 can be concentrated by cell size selection using 0.45-microm-pore-size filters, but not by using 0.22-microm-pore-size filters. OD1, OP11, TM7 and OP5 bacteria have yet to be cultivated; therefore, our concentration method may be used as an initial step in studies to analyze the structural properties of OD1, OP11, and TM7 bacteria.

摘要

对16S核糖体RNA基因(rDNA)的分子分析表明,根际微生物群落高度复杂。为了系统地表征根际细菌的细胞大小,我们选择了可能能通过0.22微米或0.45微米孔径过滤器的细菌,然后使用通用引物对27F/1492R和63F/1387R对16S rDNA基因进行PCR扩增。从通过0.45微米孔径过滤器的细菌中提取的PCR扩增rDNA在电泳后的琼脂糖凝胶中可以检测到;而在细菌通过0.22微米孔径过滤器后,未发现PCR扩增的rDNA。对有或没有细胞大小选择的PCR扩增rDNA文库进行随机克隆和测序的比较表明,属于候选系统发育分支OD1(源自OP11的1)、OP11、TM7和OP5的细菌可以通过使用0.45微米孔径过滤器进行细胞大小选择来浓缩,但不能通过使用0.22微米孔径过滤器来浓缩。OD1、OP11、TM7和OP5细菌尚未培养;因此,我们的浓缩方法可作为分析OD1、OP11和TM7细菌结构特性研究的第一步。

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