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加拿大纸浆和造纸活性污泥中微生物群落的分子特征及一种新型类艾氏硫丝菌膨胀丝状体的定量分析

Molecular characterization of microbial communities in Canadian pulp and paper activated sludge and quantification of a novel Thiothrix eikelboomii-like bulking filament.

作者信息

Dumonceaux Tim J, Hill Janet E, Pelletier Carl P, Paice Michael G, Van Kessel Andrew G, Hemmingsen Sean M

机构信息

Department of Animal and Poultry Science, University of Saskatchewan, Canada.

出版信息

Can J Microbiol. 2006 May;52(5):494-500. doi: 10.1139/w05-160.

Abstract

We examined the microbial community structure and quantified the levels of the filamentous bulking organism Thiothrix eikelboomii in samples of activated sludge mixed liquor suspended solids (MLSS) from Canadian pulp and paper mills. Libraries of chaperonin 60 (cpn60) gene sequences were prepared from MLSS total microbial community DNA and each was compared with cpnDB, a reference database of cpn60 sequences (http://cpndb.cbr.nrc.ca) for assignment of taxonomic identities. Sequences similar to but distinct from the type strain of T. eikelboomii AP3 (ATCC 49788T) (approximately 89% identity over 555 bp) were recovered at high frequency from a mill sample that was experiencing bulking problems at the time of sample collection, which corresponded to microscopic observations using fluorescent in situ hybridization with commercially available 16S rDNA-based probes. We enumerated this strain in five mill-derived MLSS samples using real-time quantitative PCR (qPCR) and found that two samples had high levels of the bulking strain (>1012 genomes/g MLSS) and two contained lower but detectable levels of this organism. None of the mill samples contained cpn60 sequences that were identical to the type strain of T. eikelboomii. This technique shows promise for monitoring pulp and paper mill wastewater treatment systems by detecting and enumerating this strain of T. eikelboomii, which may be specific to pulp and paper mill wastewater treatment systems.

摘要

我们研究了加拿大纸浆和造纸厂活性污泥混合液悬浮固体(MLSS)样本中的微生物群落结构,并对丝状膨胀微生物艾氏硫丝菌(Thiothrix eikelboomii)的水平进行了定量分析。从MLSS总微生物群落DNA制备伴侣蛋白60(cpn60)基因序列文库,并将每个文库与cpnDB(cpn60序列的参考数据库,http://cpndb.cbr.nrc.ca)进行比较,以确定分类身份。在样本采集时出现膨胀问题的一家工厂样本中,高频回收了与艾氏硫丝菌AP3模式菌株(ATCC 49788T)相似但不同的序列(在555 bp上约89%的同一性),这与使用市售基于16S rDNA的探针进行荧光原位杂交的显微镜观察结果一致。我们使用实时定量PCR(qPCR)对五个工厂来源的MLSS样本中的该菌株进行计数,发现两个样本中膨胀菌株水平较高(>1012个基因组/g MLSS),另外两个样本中该微生物水平较低但可检测到。没有一个工厂样本包含与艾氏硫丝菌模式菌株相同的cpn60序列。该技术通过检测和计数这种可能特定于纸浆和造纸厂废水处理系统的艾氏硫丝菌菌株,显示出监测纸浆和造纸厂废水处理系统的前景。

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