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颗粒生物膜中微生物群落的均一性和同步动力学:从主要种群到次要群体。

Homogeneity and synchronous dynamics of microbial communities in particulate biofilms: from major populations to minor groups.

机构信息

INRA, UR50, Laboratoire de Biotechnologie de l'Environnement, Avenue des Etangs, Narbonne, F-11100, France.

出版信息

Microbes Environ. 2012;27(2):142-8. doi: 10.1264/jsme2.me11264.

Abstract

Natural or engineered microbial populations often show variations over time. These variations may be due to environmental fluctuations or intrinsic factors. Thus, studying the dynamics of microbial diversity for different communities living in a spatially homogeneous landscape is of interest. As a model ecosystem, nitrifying biofilm communities were grown in a two litre inverse turbulent bed reactor (ITBR) containing an estimated 200 million small particles (about 150 µm in diameter). Each particulate biofilm is considered as a distinct community growing in the neighborhood of other similar particles, in a homogeneous and well-controlled environmental context. A molecular approach was adopted to test how microbial community structures might evolve: either in synchrony, converging or diverging. The shape of biofilm was observed by microscopy for each particle. The biomass content was evaluated by quantitative PCR and showed similar values for each particle. The microbial community structure was evaluated by Capillary Electrophoresis-Single Strand Conformation Polymorphism (CE-SSCP) fingerprinting and showed extraordinary homogeneity between particles, even though transitory community structures were observed when reactor operating conditions were modified. This homogeneity was observed for the Bacteria primer set but, more interestingly, was also observed when minor non-nitrifying bacteria making up the biofilm, representing about 5% and 10% of total cells, were targeted.

摘要

自然或工程微生物群体通常随时间表现出变化。这些变化可能是由于环境波动或内在因素引起的。因此,研究在空间均一景观中生活的不同群落的微生物多样性动态是很有意义的。作为一个模型生态系统,硝化生物膜群落在含有约 2 亿个小颗粒(直径约 150μm)的 2 升反向湍流床反应器(ITBR)中生长。每个颗粒状生物膜都被认为是在其他类似颗粒的附近生长的独特群落,处于同质且受良好控制的环境背景中。采用分子方法来检验微生物群落结构可能如何演变:同步、趋同或趋异。通过显微镜观察每个颗粒的生物膜形状。通过定量 PCR 评估生物量含量,每个颗粒的含量相似。通过毛细管电泳-单链构象多态性(CE-SSCP)指纹图谱评估微生物群落结构,即使在改变反应器运行条件时观察到短暂的群落结构,颗粒之间也表现出极高的同质性。这种同质性不仅在细菌引物组中观察到,而且在构成生物膜的占总细胞约 5%和 10%的次要非硝化细菌中也观察到,这更有趣。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ee5/4036020/debb37b8841e/27_142f1.jpg

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