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通过对PCR扩增的16S rRNA基因进行限制性片段长度多态性分析来估计与海草针叶藻相关的未培养微生物的多样性。

Diversity of uncultured microorganisms associated with the seagrass Halophila stipulacea estimated by restriction fragment length polymorphism analysis of PCR-amplified 16S rRNA genes.

作者信息

Weidner S, Arnold W, Puhler A

机构信息

Fakultat fur Biologie, Lehrstuhl fur Genetik, Universitat Bielefeld, Germany.

出版信息

Appl Environ Microbiol. 1996 Mar;62(3):766-71. doi: 10.1128/aem.62.3.766-771.1996.

Abstract

The diversity of microorganisms associated with the leaves of the seagrass Halophila stipulacea in the northern Gulf of Elat was examined by culture-independent analysis. Microorganisms were harvested by a sonication treatment for total-community genomic DNA isolation. Oligonucleotides complementary to conserved regions in the 16S rRNA-encoding DNA (rDNA) of bacteria were used for PCR amplification. The 16S rDNA PCR products were subcloned and further characterized by a restriction fragment length analysis termed ARDRA (amplified rDNA restriction analysis). These analyses were carried out after reamplifying the cloned fragments with two primers binding symmetrically to the plasmid immediately on both sides of the cloned insert. Computer-aided clustering was performed after separate restriction analysis with enzymes HinfI and HpaII. By this method, 103 cloned 16S rDNA fragments were clustered into a total of 58 different groups. Sequence analysis of clones with an identical ARDRA pattern confirmed that members of an ARDRA group were closely related to each other. The sequenced clones were found to be affiliated with a marine snow-associated plastid-like rRNA clone and with a marine Hyphomonas strain, respectively. The method applied in this study could be useful for the routine study of other microbial communities of interest.

摘要

通过非培养分析方法,对埃拉特湾北部的海草哈氏海篷子叶片相关的微生物多样性进行了研究。采用超声处理收获微生物,以提取总群落基因组DNA。使用与细菌16S rRNA编码DNA(rDNA)保守区域互补的寡核苷酸进行PCR扩增。16S rDNA PCR产物进行亚克隆,并通过一种称为ARDRA(扩增rDNA限制性分析)的限制性片段长度分析进一步表征。在用与克隆插入片段两侧的质粒对称结合的两种引物对克隆片段进行再扩增后,进行这些分析。用HinfI和HpaII酶分别进行限制性分析后,进行计算机辅助聚类。通过这种方法,103个克隆的16S rDNA片段总共被聚类为58个不同的组。对具有相同ARDRA模式的克隆进行序列分析证实,一个ARDRA组的成员彼此密切相关。发现测序的克隆分别与一个与海雪相关的类质体rRNA克隆和一个海洋生丝单胞菌菌株相关。本研究中应用的方法可能对其他感兴趣的微生物群落的常规研究有用。

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