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Enrichment and characterization of an anaerobic cellulolytic microbial consortium SQD-1.1 from mangrove soil

机译:红树林土壤中厌氧纤维素分解微生物群SQD-1.1的富集和表征

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Enrichment of microbial consortia provides an approach to simulate and investigate microbial communities in natural environments. In this study, a cellulolytic microbial consortium SQD-1.1 was enriched from mangrove soil of Qinglan port (Hainan, China) by 27 times continuous subcultivation under anaerobic static conditions. The consortium could completely degrade 0.2 % (w/v) filter paper within 3 days and utilized it as the sole carbon source. PCRdenaturing gradient gel electrophoresis analysis revealed a stable microbial community structure in the incubation process of 10 days and in the procedure of subcultivation. Twenty-four operational taxonomic units belonging to seven phyla were obtained from the full-length 16S rRNA gene library. Five clones, closest related to the genera Alkaliflexus, Clostridium, Alistipes, Spirochaeta, and Trichococcus, were the predominant ones. Among them, M117, phylogeneticly showing high similarity (16S rRNA gene identity, 95.3 %) with the cellulolytic anaerobic bacterium Clostridium straminisolvens CSK1~T, was the potential key cellulolytic bacterium. Using the plate cultivation method, 12 strains, including one potential new species and four potential new species of new genera, were isolated. The strain P2, corresponding to the most frequently detected clone (M05) in the 16S rRNA gene library, showed both CMCase and xylanase activity and may be another important cellulolytic bacterium. The findings of cellulase activity in cell pellet and cohesion and dockerin domains in metagenome data further suggested the potential of utilization of cellulosomes by the consortium to degrade cellulose. Consortium SQD-1.1 provides a candidate for investigating the mechanism of cellulose degradation under anoxic conditions in natural environments.
机译:微生物群落的富集提供了一种模拟和研究自然环境中微生物群落的方法。在本研究中,通过在厌氧静态条件下连续传代27次,从青兰港(中国海南)的红树林土壤中富集了纤维素分解微生物群SQD-1.1。该财团可以在3天内完全降解0.2%(w / v)的滤纸,并将其用作唯一的碳源。 PCR变性梯度凝胶电泳分析显示,在10天的培养过程中和在亚培养过程中,微生物群落结构稳定。从全长16S rRNA基因文库中获得了属于七个门的二十四个操作分类单元。最主要的克隆有五个,分别与碱弯曲杆菌属,梭菌属,阿利斯培斯属,螺旋体属和毛球菌属有关。其中,M117与潜在的纤维素分解厌氧细菌Clostridium straminisolvens CSK1〜T在系统发育上具有很高的相似性(16S rRNA基因同一性,为95.3%)。使用平板培养方法,分离了12个菌株,包括一个潜在的新物种和四个潜在的新物种。对应于16S rRNA基因库中最常检测到的克隆(M05)的P2菌株同时显示CMCase和木聚糖酶活性,可能是另一种重要的纤维素分解细菌。在元基因组数据中细胞沉淀和凝聚域以及dockerin域中纤维素酶活性的发现进一步表明,财团利用纤维素体降解纤维素的潜力。 Consortium SQD-1.1为研究自然环境中缺氧条件下纤维素降解的机理提供了一个候选方案。

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