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The metagenome of a biogas-producing microbial community of a production-scale biogas plant fermenter analysed by the 454-pyrosequencing technology

机译:通过454焦磷酸测序技术分析的生产规模沼气发酵罐中产生沼气的微生物群落的元基因组

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Composition and gene content of a biogas-producing microbial community from a production-scale biogas plant fed with renewable primary products was analysed by means of a metagenomic approach applying the ultrafast 454-pyrosequencing technology. Sequencing of isolated total community DNA on a Genome Sequencer FLX System resulted in 616,072 reads with an average read length of 230 bases accounting for 141,664,289 bases sequence information. Assignment of obtained single reads to COG (Clusters of Orthologous Groups of proteins) categories revealed a genetic profile characteristic for an anaerobic microbial consortium conducting fermentative metabolic pathways. Assembly of single reads resulted in the formation of 8752 contigs larger than 500 bases in size. Contigs longer than 10kb mainly encode house-keeping proteins, e.g. DNA polymerase, recombinase, DNA ligase, sigma factor RpoD and genes involved in sugar and amino acid metabolism. A significant portion of contigs was allocated to the genome sequence of the archaeal methanogen Methanoculleus marisnigri JR1. Mapping of single reads to the M. marisnigri JR1 genome revealed that approximately 64% of the reference genome including methanogenesis gene regions are deeply covered. These results suggest that species related to those of the genus Methanoculleus play a dominant role in methanogenesis in the analysed fermentation sample. Moreover, assignment of numerous contig sequences to clostridial genomes including gene regions for cellulolytic functions indicates that clostridia are important for hydrolysis of cellulosic plant biomass in the biogas fermenter under study. Metagenome sequence data from a biogas-producing microbial community residing in a fermenter of a biogas plant provide the basis for a rational approach to improve the biotechnological process of biogas production.
机译:通过采用超快454-焦磷酸测序技术的宏基因组学方法,对采用可再生初级产品喂养的生产规模沼气厂中产生沼气的微生物群落的组成和基因含量进行了分析。在Genome Sequencer FLX系统上对分离的总群落DNA进行测序,得到616,072条读物,平均读长为230个碱基,占141,664,289个碱基的序列信息。将获得的单读片段分配给COG(蛋白质直系同源簇)类别,揭示了进行发酵代谢途径的厌氧微生物财团的遗传特征。单读的组装导致形成了大小超过500个碱基的8752个重叠群。长度超过10kb的重叠群主要编码持家蛋白,例如DNA聚合酶,重组酶,DNA连接酶,σ因子RpoD以及参与糖和氨基酸代谢的基因。重叠群的很大一部分分配给了古细菌产甲烷菌Marisnigri JR1的基因组序列。将单读物映射到M. marisnigri JR1基因组表明,包括甲烷生成基因区域在内的参考基因组约有64%被深层覆盖。这些结果表明,在所分析的发酵样品中,与甲烷菌属相关的物种在甲烷生成中起主要作用。此外,将大量重叠群序列分配给包括纤维素分解功能基因区域的梭菌基因组表明梭状芽胞杆菌对于所研究的沼气发酵罐中的纤维素植物生物质的水解很重要。来自位于沼气厂发酵罐中的产生沼气的微生物群落的元基因组序列数据,为改善沼气生产生物技术过程的合理方法提供了基础。

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