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首页> 外文期刊>Journal of industrial microbiology & biotechnology >Molecular insight into activated sludge producing polyhydroxyalkanoates under aerobic-anaerobic conditions.
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Molecular insight into activated sludge producing polyhydroxyalkanoates under aerobic-anaerobic conditions.

机译:在好氧-厌氧条件下生产活性污泥的聚羟基链烷酸酯的分子洞察力。

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摘要

One of the options enabling more economic production of polyhydroxyalkanoates compared to pure cultures is the application of mixed cultures. The use of a microbial community in a sequencing batch reactor has a few advantages: a simple process control, no necessity for sterile processing, and possibilities of using cheap substrates as a source of carbon. Nevertheless, while cultivation methods to achieve high PHAs biomass concentration and high productivity in wild and recombinant strains are defined, knowledge about the cultivation strategy for PHAs production by mixed culture and species composition of bacterial communities is still very limited. The main object of this study was to characterize on the molecular level the composition and activity of PHAs producing microorganism in activated sludge cultivated under oxygen limitation conditions. PHAs producers were detected using a PCR technique and the created PHA synthase gene library was analyzed by DNA sequencing. The obtained results indicate that PHAs-producers belonged to Pseudomonas sp., and possessed genes coding for mcl-PHA synthase. The kinetics of mcl-PHA synthase expression was relatively estimated using real-time PCR technology at several timepoints. Performed quantitative and qualitative analysis of total bacterial activity showed that there were differences in total activity during the process but differential expression of various groups of microorganisms examined by using DGGE was not observed.
机译:与纯培养物相比,能够更经济地生产聚羟基链烷酸酯的一种选择是混合培养物的应用。在顺序批处理反应器中使用微生物群落具有一些优点:简单的过程控制,无需进行无菌处理以及使用廉价底物作为碳源的可能性。然而,尽管定义了在野生和重组菌株中实现高PHA生物量浓度和高生产率的栽培方法,但是关于通过混合培养和细菌群落物种组成生产PHA的栽培策略的知识仍然非常有限。这项研究的主要目的是在分子水平上表征在限制氧条件下培养的活性污泥中产生PHA的微生物的组成和活性。使用PCR技术检测PHAs产生者,并通过DNA测序分析创建的PHA合酶基因文库。获得的结果表明,PHA生产者属于假单胞菌属,并且具有编码mcl-PHA合酶的基因。使用实时PCR技术在几个时间点相对估计了mcl-PHA合酶表达的动力学。对总细菌活性进行的定量和定性分析表明,在此过程中总活性存在差异,但未观察到使用DGGE检测的各种微生物的差异表达。

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