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海洋氨氧化菌富集培养物的分子分析

Molecular analysis of enrichment cultures of marine ammonia oxidisers.

作者信息

McCaig A E, Embley T M, Prosser J I

机构信息

Department of Molecular and Cell Biology, University of Aberdeen, Marischal College, UK.

出版信息

FEMS Microbiol Lett. 1994 Jul 15;120(3):363-7. doi: 10.1111/j.1574-6968.1994.tb07059.x.

DOI:10.1111/j.1574-6968.1994.tb07059.x
PMID:8076810
Abstract

Marine ammonia oxidising bacteria were enriched by incubation of sea water, amended with ammonium sulphate, and subsequent subculture in liquid inorganic medium. PCR primers were designed to be specific for rDNA sequences from ammonia oxidisers belonging to the beta-sub-group of the proteobacteria. These primers were then used to amplify rRNA genes from ammonia oxidiser enrichment cultures containing heterotrophs. PCR products were recovered from all cultures in which complete ammonia oxidation occurred. Subsequent rDNA sequence analysis indicated the presence of three new lineages within the clade defined by sequences of cultured beta-sub-group ammonia oxidisers. Two of the new lineages showed moderate similarity to sequences from pure cultures of ammonia oxidisers previously isolated from marine and brackish environments. The third lineage (AEM-3) was deep branching and occupied an intermediate position between clades defined by Nitrosomonas or Nitrosospira, which were isolated from soil or sewage. The phylogenetic analysis suggests that, in enrichment cultures, the primers are specific for members of the target group, the beta-proteobacteria ammonia oxidisers. The results also indicate the presence of previously unknown ammonia oxidisers in marine samples. The approach enabled analysis of ammonia oxidiser enrichments at an early stage and without the requirement for isolation of pure cultures, significantly reducing the time required and facilitating quantitative assessment of relatedness of strains.

摘要

通过用硫酸铵改良海水并随后在液体无机培养基中传代培养来富集海洋氨氧化细菌。设计PCR引物,使其对属于变形菌β亚群的氨氧化菌的rDNA序列具有特异性。然后用这些引物从含有异养菌的氨氧化菌富集培养物中扩增rRNA基因。从所有发生完全氨氧化的培养物中回收PCR产物。随后的rDNA序列分析表明,在由培养的β亚群氨氧化菌序列定义的进化枝内存在三个新谱系。其中两个新谱系与先前从海洋和微咸水环境中分离的氨氧化菌纯培养物的序列有中等程度的相似性。第三个谱系(AEM-3)分支较深,位于从土壤或污水中分离出的亚硝化单胞菌或亚硝化螺菌定义的进化枝之间的中间位置。系统发育分析表明,在富集培养物中,引物对目标菌群β-变形菌氨氧化菌具有特异性。结果还表明,海洋样品中存在以前未知的氨氧化菌。该方法能够在早期阶段对氨氧化菌富集物进行分析,而无需分离纯培养物,显著减少了所需时间,并便于对菌株的亲缘关系进行定量评估。

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