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Detection of abundant sulphate-reducing bacteria in marine oxic sediment layers by a combined cultivation and molecular approach

机译:结合培养和分子生物学方法检测海洋含氧沉积物层中大量减少硫酸盐的细菌

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The depth distribution and diversity of sulphate-reducing bacteria (SRB) was analysed in the upper intertidal zone of a sandy marine sediment of the Dutch island Schiermonnikoog. The upper centimetre of the sediment included the oxic- anoxic interface and was cut into five slices. With each slice, most probable number (MPN) dilution series were set up in microtitre plates using five different substrates. In the deeper sediment layers, up to 1 * 10~8 cm~(-3) lactate-utilizing SRB were counted. corresponding to 23% of the total bacterial count. From the highest positive dilutions of the MPN series, 27 strains of SRB were isolated in pure culture.Sequencing of a 580 bp fragment of the 16S rDNA revealed that 21 isolates had identical sequences, also identical with that of the previously described species Desulfomicrobium apsheronum. However, the diversity of the isolates was higher with respect to their physiological properties: a total of 11 different phenotypes could be distinguished. Genomic fingerprinting by enterobacterial repetitive intergenic consensus (ERIC) polymerase chain reaction (PCR) revealed an even higher diversity of 22 different genotypes. A culture-independent analysis by PCR and denaturing -gradient gel electrophoresis (DGGE) revealed that the partial 16S rDNA sequence of the isolated D. apsheronum strains constituted a significant fraction of the Desulfovi-brionaceae. The high subspecies diversity suggests that this abundant aggregate-forming species may have evolved adaptations to different ecological niches in the oxic sediment layers.
机译:在荷兰小岛Schiermonnikoog的沙质海洋沉积物的上潮间带分析了硫酸盐还原细菌(SRB)的深度分布和多样性。沉积物的上厘米包括有氧-缺氧界面,被切成五段。对于每个切片,使用五个不同的底物在微量滴定板上设置最可能的稀释倍数系列。在较深的沉积层中,计数到高达1 * 10〜8 cm〜(-3)的利用乳酸的SRB。相当于细菌总数的23%。从MPN系列的最高阳性稀释液中,在纯培养物中分离出27株SRB。对16S rDNA的580 bp片段进行测序发现,有21个分离株具有相同的序列,也与前面描述的脱硫微囊藻相同。但是,分离物的生理特性更高,可以区分出总共11种不同的表型。通过肠细菌重复基因间共有(ERIC)聚合酶链反应(PCR)进行的基因组指纹分析显示,22种不同基因型的多样性更高。通过PCR和变性梯度凝胶电泳(DGGE)进行的不依赖培养的分析表明,分离出的毒死ps药菌株的部分16S rDNA序列构成了脱硫弧菌科的重要组成部分。高亚种的多样性表明,这种形成大量聚集体的物种可能已经适应了含氧沉积物层中不同生态位。

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