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来自啤酒酿造腐败菌嗜酵母果胶杆菌和弗里斯兰果胶杆菌的鞭毛蛋白基因及蛋白。

The flagellin gene and protein from the brewing spoilage bacteria Pectinatus cerevisiiphilus and Pectinatus frisingensis.

作者信息

Chaban Bonnie, Deneer Harry, Dowgiert Teri, Hymers Jillian, Ziola Barry

机构信息

Department of Microbiology and Immunology, Queen's University, Kingston, ON, Canada.

出版信息

Can J Microbiol. 2005 Oct;51(10):863-74. doi: 10.1139/w05-076.

Abstract

Flagellin genes from the anaerobic Gram-negative beer-spoilage bacteria Pectinatus cerevisiiphilus and Pectinatus frisingensis were sequenced and the flagellin proteins initially characterized. Protein microsequencing led to the design of two degenerate PCR primers that allowed the P. cerevisiiphilus flagellin gene to be partially sequenced. A combination of PCR and Bubble PCR was then used to sequence the flagellin genes of three isolates from each species. Cloning and gene expression, followed by immunoblotting, confirmed the gene identities as flagellin. Analysis of the gene sequences revealed proteins similar to other bacterial flagellins, including lengths of 446 or 448 amino acids, putative sigma 28 promoters, and a termination loop. Antibody binding studies with isolated flagella correlated with gene sequence comparisons, with both indicating that the P. cerevisiiphilus isolates studied are very similar but that the P. frisingensis isolates show greater variation. Purified flagellins were found to be glycosylated, probably through an O linkage. Phylogenetic analysis revealed greater diversity within the flagellin sequences than within the 16S rRNA genes. Despite the Gram-negative morphology of Pectinatus, this genus proved most closely related to Gram-positive Firmicutes.

摘要

对厌氧革兰氏阴性啤酒腐败菌酿酒果胶杆菌(Pectinatus cerevisiiphilus)和弗里斯兰果胶杆菌(Pectinatus frisingensis)的鞭毛蛋白基因进行了测序,并对鞭毛蛋白进行了初步表征。蛋白质微量测序促使设计了两种简并PCR引物,从而得以对酿酒果胶杆菌的鞭毛蛋白基因进行部分测序。然后,采用PCR和气泡PCR相结合的方法对每个物种的三个分离株的鞭毛蛋白基因进行测序。通过克隆和基因表达,随后进行免疫印迹,证实了这些基因确为鞭毛蛋白基因。对基因序列的分析揭示了与其他细菌鞭毛蛋白相似的蛋白质,包括长度为446或448个氨基酸、推定的σ28启动子和一个终止环。对分离出的鞭毛进行的抗体结合研究与基因序列比较结果相关,两者均表明所研究的酿酒果胶杆菌分离株非常相似,但弗里斯兰果胶杆菌分离株显示出更大的变异性。发现纯化的鞭毛蛋白被糖基化,可能是通过O-连接。系统发育分析表明,鞭毛蛋白序列中的多样性大于16S rRNA基因中的多样性。尽管果胶杆菌具有革兰氏阴性形态,但该属被证明与革兰氏阳性厚壁菌门关系最为密切。

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