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用于评估瘤胃纤维素分解菌黄化瘤胃球菌多样性的纤维小体基因簇分析

Cellulosome gene cluster analysis for gauging the diversity of the ruminal cellulolytic bacterium Ruminococcus flavefaciens.

作者信息

Jindou Sadanari, Brulc Jennifer M, Levy-Assaraf Maly, Rincon Marco T, Flint Harry J, Berg Margret E, Wilson Melissa K, White Bryan A, Bayer Edward A, Lamed Raphael, Borovok Ilya

机构信息

Department of Molecular Microbiology and Biotechnology, Tel Aviv University, Ramat Aviv, Israel.

出版信息

FEMS Microbiol Lett. 2008 Aug;285(2):188-94. doi: 10.1111/j.1574-6968.2008.01234.x. Epub 2008 Jun 28.

DOI:10.1111/j.1574-6968.2008.01234.x
PMID:18564339
Abstract

Ruminococcus flavefaciens is a vital cellulosome-producing fibrolytic rumen bacterium. The arrangement of the cellulosomal scaffoldin gene cluster (scaC-scaA-scaB-cttA-scaE) is conserved in two R. flavefaciens strains (17 and FD-1). Sequence analysis revealed a high mosaic conservation of the intergenic regions in the two strains that contrasted sharply with the divergence of the structural sca gene sequences. Based on the conserved intergenic regions, we designed PCR primers in order to examine the sca gene cluster in additional R. flavefaciens strains (C94, B34b, C1a and JM1). Using these conserved and/or degenerate primers, the scaC, scaA and scaB genes were amplified in all six strains, while the entire sca gene cluster and the proximal genes cttA and scaE were successfully amplified in four of the strains (17, FD-1, C94 and JM1). The sequencing of scaA and scaC genes in all the strains yielded additional insight into the variability of the structural genes with regard to the number and type of cohesin modules contained in a conserved molecular skeleton. Moreover, the scaC gene, being short and variable, appears to be a promising functional phylotyping target for metagenomic population studies of R. flavefaciens in the rumen as a function of the individual host animal.

摘要

黄化瘤胃球菌是一种重要的能产生纤维小体的瘤胃纤维分解菌。纤维小体支架蛋白基因簇(scaC - scaA - scaB - cttA - scaE)的排列在两株黄化瘤胃球菌(17株和FD - 1株)中是保守的。序列分析显示,这两株菌的基因间隔区存在高度镶嵌保守性,这与结构sca基因序列的差异形成鲜明对比。基于保守的基因间隔区,我们设计了PCR引物,以检测其他黄化瘤胃球菌菌株(C94、B34b、C1a和JM1)中的sca基因簇。使用这些保守和/或简并引物,在所有六株菌中均扩增出了scaC、scaA和scaB基因,而在其中四株菌(17株、FD - 1株、C94株和JM1株)中成功扩增出了完整的sca基因簇以及近端基因cttA和scaE。对所有菌株中scaA和scaC基因的测序,使我们对结构基因在保守分子骨架中所含黏附素模块的数量和类型方面的变异性有了更多了解。此外,scaC基因短小且具有变异性,作为个体宿主动物的一个函数,它似乎是瘤胃中黄化瘤胃球菌宏基因组群体研究中一个很有前景的功能系统发育分型靶点。

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