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SUP05 Dominates the Gammaproteobacterial Sulfur Oxidizer Assemblages in Pelagic Redoxclines of the Central Baltic and Black Seas

机译:SUP05在中波罗的海和黑海的中上层氧化还原系中占主导地位的γ-蛋白细菌硫氧化器组合

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Gammaproteobacterial sulfur oxidizers (GSOs), particularly SUP05-related sequences, have been found worldwide in numerous oxygen-deficient marine environments. However, knowledge regarding their abundance, distribution, and ecological role is scarce. In this study, on the basis of phylogenetic analyses of 16S rRNA gene sequences originating from a Baltic Sea pelagic redoxcline, the in situ abundances of different GSO subgroups were quantified by CARD-FISH (catalyzed reporter fluorescence in situ hybridization) with oligonucleotide probes developed specifically for this purpose. Additionally, ribulose bisphosphate carboxylase/oxygenase form II ( cbbM ) gene transcript clone libraries were used to detect potential active chemolithoautotrophic GSOs in the Baltic Sea. Taken together, the results obtained by these two approaches demonstrated the existence of two major phylogenetic subclusters embedded within the GSO, one of them affiliated with sequences of the previously described SUP05 subgroup. CARD-FISH analyses revealed that only SUP05 occurred in relatively high numbers, reaching 10 to 30% of the total prokaryotes around the oxic-anoxic interface, where oxygen and sulfide concentrations are minimal. The applicability of the oligonucleotide probes was confirmed with samples from the Black Sea redoxcline, in which the SUP05 subgroup accounted for 10 to 13% of the total prokaryotic abundance. The cbbM transcripts presumably originating from SUP05 cells support previous evidence for the chemolithoautotrophic activity of this phylogenetic group. Our findings on the vertical distribution and high abundance of SUP05 suggest that this group plays an important role in marine redoxcline biogeochemistry, probably as anaerobic or aerobic sulfur oxidizers.
机译:在许多缺氧的海洋环境中,全球都发现了γ-变形细菌硫氧化剂(GSO),特别是与SUP05相关的序列。但是,关于它们的丰度,分布和生态作用的知识很少。在这项研究中,在对来自波罗的海中上层氧化还原细胞的16S rRNA基因序列进行系统发育分析的基础上,使用专门开发的寡核苷酸探针,通过CARD-FISH(催化的报告荧光原位杂交)定量了不同GSO亚组的原位丰度。以此目的。此外,使用核糖二磷酸羧化酶/加氧酶II(cbbM)基因转录本克隆文库来检测波罗的海潜在的活性化营养自养GSO。综上所述,通过这两种方法获得的结果证明了存在于GSO中的两个主要系统发育亚群的存在,其中一个与先前描述的SUP05子群的序列有关。 CARD-FISH分析表明,只有SUP05发生的数量相对较高,达到了氧-硫界面的原核生物总数的10%至30%,其中氧和硫化物的浓度极低。寡核苷酸探针的适用性已被黑海氧化还原酶的样品证实,其中SUP05亚组占原核生物总丰度的10%至13%。推测源自SUP05细胞的cbbM转录本为该系统发生组的化石自养能力提供了先前的证据。我们对SUP05的垂直分布和高丰度的发现表明,该组在海洋氧化还原碱生物地球化学中起着重要作用,可能作为厌氧或好氧的硫氧化剂。

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