Sara Kleindienst, Lubos Polerecky, Rudolf Amann, Florin Musat, Katrin Knittel
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引用次数: 0
摘要
海洋烃类渗漏是硫酸盐还原耦合烃类氧化的热点。然而,硫酸盐还原细菌(SRB)降解除甲烷以外的碳氢化合物的原位代谢率仍然知之甚少。在这里,我们评估了Desulfosarcinaceae分支SCA1, SCA2降解正丁烷和分支LCA2降解正十二烷的环境作用。CARD-FISH定量分析显示,在最近重新分类的三角洲变形菌中,SCA1占31%,SCA2占9%,LCA2占6%。在Amon泥火山和Guaymas盆地沉积物中,通过稳定同位素探测结合NanoSIMS和建模估计的细胞特异性氧化速率分别为~0.73和~2.11 fmol丁烷细胞- 1 d - 1, LCA2的氧化速率为~0.023 fmol十二烷细胞- 1 d - 1。细胞碳同化、溶解无机碳产量和硫酸盐还原率表明,降解丁烷的SRB比利用十二烷的SRB具有更高的代谢活性。基于原位细胞丰度、生物体积和细胞活动的估计表明,在某些渗漏中,SCA1、SCA2和LCA2分支几乎占了所有非甲烷氧化驱动的硫酸盐还原。这些发现突出了烷烃降解SRB在影响海洋碳和硫循环方面的重要作用,特别是在排放高级碳氢化合物的渗漏处。
In Situ Metabolic Rates of Alkane-Degrading Sulphate-Reducing Bacteria in Hydrocarbon Seep Sediments Revealed by Combining CARD-FISH, NanoSIMS, and Mathematical Modelling
Marine hydrocarbon seeps are hotspots for sulphate reduction coupled to hydrocarbon oxidation. In situ metabolic rates of sulphate-reducing bacteria (SRB) degrading hydrocarbons other than methane, however, remain poorly understood. Here, we assessed the environmental role of Desulfosarcinaceae clades SCA1, SCA2 for degradation of n-butane and clade LCA2 for n-dodecane. Quantification by CARD-FISH showed that SCA1 constituted up to 31%, SCA2 up to 9%, and LCA2 up to 6% of cells from the recently re-classified class Deltaproteobacteria across diverse hydrocarbon seeps. Cell-specific oxidation rates estimated by stable-isotope probing combined with NanoSIMS and modelling were ~0.73 and ~2.11 fmol butane cell−1 d−1 for SCA1 and SCA2, respectively, and ~0.023 fmol dodecane cell−1 d−1 for LCA2 in sediments from Amon Mud Volcano and Guaymas Basin sediments. Cellular carbon assimilation, dissolved inorganic carbon production, and sulphate reduction rates indicated that butane-degrading SRB have higher metabolic activity than those utilising dodecane. Estimates based on in situ cell abundances, biovolumes, and cellular activities suggest that at certain seeps, clades SCA1, SCA2 and LCA2 account for nearly all sulphate reduction not driven by methane oxidation. These findings highlight the important role of alkane-degrading SRB in influencing marine carbon and sulphur cycles, particularly at seeps emitting higher hydrocarbons.
期刊介绍:
Environmental Microbiology provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following:
the structure, activities and communal behaviour of microbial communities
microbial community genetics and evolutionary processes
microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors
microbes in the tree of life, microbial diversification and evolution
population biology and clonal structure
microbial metabolic and structural diversity
microbial physiology, growth and survival
microbes and surfaces, adhesion and biofouling
responses to environmental signals and stress factors
modelling and theory development
pollution microbiology
extremophiles and life in extreme and unusual little-explored habitats
element cycles and biogeochemical processes, primary and secondary production
microbes in a changing world, microbially-influenced global changes
evolution and diversity of archaeal and bacterial viruses
new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens