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首页> 外文期刊>Water Science and Technology >Quantitative fluorescent in-situ hybridization: a hypothesized competition mode between two dominant bacteria groups in hydrogen-producing anaerobic sludge processes
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Quantitative fluorescent in-situ hybridization: a hypothesized competition mode between two dominant bacteria groups in hydrogen-producing anaerobic sludge processes

机译:定量荧光原位杂交:产氢厌氧污泥过程中两个主要细菌群之间的假设竞争模式

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Two hydrogen-producing continuous flow stirred tank reactors (CSTRs) fed respectively with glucose and sucrose were investigated by polymerase chain reaction-denatured gradient gel electrophoresis (PCR-DGGE) and fluorescent in-situ hybridization (FISH). The substrate was fed in a continuous mode decreased from hydraulic retention time (HRT) 10 hours to 6, 5, 4, 3, and 2 hours. Quantitative fluorescent in-situ hybridization (FISH) observations further demonstrated that two morphotypes of bacteria dominated both microbial communities. One was long rod bacteria which can be targeted either by Chis150 probe designed to hybridize the gram positive low G+C bacteria or the specific oligonucleotide probe Lg10-6. The probe Lg10-6, affiliated with Clostridium pasteurianum, was designed and then checked with other reference organisms. The other type, unknown group, which cannot be detected by Chis150 was curved rod bacteria. Notably, the population ratios of the two predominant groups reflected the different operational performance of the two reactors, such as hydrogen producing rates, substrate turnover rates and metabolites compositions. Therefore, a competition mode of the two dominant bacteria groups was hypothesized. In the study, 16S rRNA-based gene library of hydrogen-producing microbial communities was established. The efficiency of hydrogen yields was correlated with substrates (glucose or sucrose), HRT, metabolites compositions (acetate, propionate, butyrate and ethanol), thermal pre-treatment (seed biomass was heated at 100C for 45 minutes), and microbial communities in the bioreactor, not sludge sources (municipal sewage sludge, alcohol-processing sludge, or bean-processing sludge). The designed specific oligonucleotide probe Lg10-6 also provides us a useful and fast molecular tool to screen hydrogen-producing microbial communities in the future research.
机译:通过聚合酶链反应-变性梯度凝胶电泳(PCR-DGGE)和荧光原位杂交(FISH)研究了两个分别供入葡萄糖和蔗糖的产氢连续流搅拌釜反应器(CSTR)。以连续模式进料基材,该时间从水力停留时间(HRT)减少了10小时到6、5、4、3和2小时。定量荧光原位杂交(FISH)观察进一步表明,两种形态的细菌主导了两个微生物群落。一种是长杆细菌,可以被设计为与革兰氏阳性低G + C细菌杂交的Chis150探针或特异性寡核苷酸探针Lg10-6靶向。设计与巴氏梭菌相关的探针Lg10-6,然后与其他参考生物进行检查。 Chis150无法检测到的另一种未知群体是弯曲杆细菌。值得注意的是,两个主要组的人口比率反映了两个反应器的不同运行性能,例如产氢率,底物周转率和代谢物组成。因此,假设了两个优势细菌群的竞争模式。在这项研究中,建立了基于16S rRNA的产氢微生物群落的基因文库。氢产量的效率与底物(葡萄糖或蔗糖),HRT,代谢产物组成(乙酸盐,丙酸盐,丁酸盐和乙醇),热预处理(种子生物质在100°C加热45分钟)以及微生物群落相关。生物反应器,而不是污泥来源(市政污水污泥,酒精加工污泥或豆类加工污泥)。设计的特异性寡核苷酸探针Lg10-6还为我们提供了一个有用的快速分子工具,可以在未来的研究中筛选产氢微生物群落。

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