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Phylogenetic description of immobilized methanogenic community using real-time PCR in a fixed-bed anaerobic digester

机译:在固定床厌氧消化池中使用实时PCR对固定化产甲烷菌群落的系统发育描述

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摘要

After immobilization of anaerobes on polyurethane foam in a thermophilic, fixed-bed, anaerobic digester supplied with acetate, the results of real-time PCR analysis indicated that the major immobilized methanogenic archaea were Methanosarcina spp., and that the major free-living methanogenic archaea were Methanosarcina and Methanobacterium spp. 16S rRNA gene densities of Methanosarcina spp. and Methanobacterium spp. immobilized on the polyurethane foam were 7.6 x 10(9) and 2.6 x 10(8) copies/cm(3) respectively. Immobilized methanogenic archaea could be concentrated 1000 times relative to those in the original anaerobically digested sludge from a completely mixed thermophilic digester supplied with cattle waste. On the other hand, immobilized bacteria could be concentrated only 10 times. The cell densities of the immobilized methanogenic archaea and bacteria were higher than those of the free-living methanogenic archaea and bacteria in the reactor. The results of clone analysis indicate that the major methanogenic archaea of the original thermophilic sludge are members of the order Methanomicrobiales, and that the major methanogenic archaea immobilized on the polyurethane foam are Methanosarcina spp., and those of the liquid phase are Methanobacterium spp. The results of the real time PCR analysis approximately agree with those of the clone analysis. These results indicate that real-time PCR analysis is useful for quantitatively describing methanogenic communities. (c) 2005 Elsevier Ltd. All rights reserved.
机译:在将厌氧菌固定在装有乙酸盐的嗜热,固定床,厌氧消化池中的聚氨酯泡沫上后,实时PCR分析的结果表明,主要的固定产甲烷菌是甲烷八叠球菌,而主要的是自由活动的产甲烷菌。分别是甲烷菌和甲烷菌。甲烷八叠球菌的16S rRNA基因密度。和甲烷杆菌属。固定在聚氨酯泡沫上的分别是7.6 x 10(9)和2.6 x 10(8)个/ cm(3)。固定化产甲烷菌的浓度相对于原来的厌氧消化污泥浓缩了1000倍,而原来的厌氧消化污泥来自供应牛粪便的完全混合的高温消化池。另一方面,固定的细菌只能浓缩10倍。固定的产甲烷菌和细菌的细胞密度高于反应器中自由活动产甲烷菌和细菌的细胞密度。克隆分析的结果表明,原始嗜热污泥的主要产甲烷古菌是甲烷微生物菌纲的成员,固定在聚氨酯泡沫上的主要产甲烷古菌是甲烷菌属,而液相的是甲烷甲烷菌。实时PCR分析的结果与克隆分析的结果大致一致。这些结果表明,实时PCR分析可用于定量描述产甲烷菌群落。 (c)2005 Elsevier Ltd.保留所有权利。

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