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Atypical Genetic Locus Associated with Constitutive Production of Enterocin B by Enterococcus faecium BFE 900

机译:粪肠球菌BFE 900组成肠球菌B的非典型遗传基因座

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A purified bacteriocin produced by Enterococcus faeciumBFE 900 isolated from black olives was shown by Edman degradation and mass spectrometric analyses to be identical to enterocin B produced byE. faecium T136 from meat (P. Casaus, T. Nilsen, L. M. Cintas, I. F. Nes, P. E. Hernández, and H. Holo, Microbiology 143:2287–2294, 1997). The structural gene was located on a 2.2-kb HindIII fragment and a 12.0-kb EcoRI chromosomal fragment. The genetic characteristics and production of EntB by E. faecium BFE 900 differed from that described so far by the presence of a conserved sequence like a regulatory box upstream of the EntB gene, and its production was constitutive and not regulated. The 2.2-kb chromosomal fragment contained the hitherto undetected immunity gene for EntB in an atypical orientation that is the reverse of that of the structural gene. Typical transport and other genes associated with bacteriocin production were not detected on the 12.0-kb chromosomal fragment containing the EntB structural gene. This makes the EntB genetic system different from most other bacteriocin systems, where transport and possible regulatory genes are clustered. EntB was subcloned and expressed by the dedicated secretion machinery of Carnobacterium piscicola LV17A. The structural gene was amplified by PCR, fused to the divergicin A signal peptide, and expressed by the general secretory pathway in Enterococcus faecalis ATCC 19433.
机译:通过埃德曼降解和质谱分析表明,从黑橄榄分离的粪肠球菌BFE 900产生的纯化细菌素与E产生的肠菌素B相同。粪便中的粪便T136(P。Casaus,T。Nilsen,L.M。Cintas,I。F. Nes,P。E.Hernández和H. Holo,《微生物学》 143:2287-2294,1997)。该结构基因位于2.2kb的HindIII片段和12.0kb的EcoRI染色体片段上。粪肠球菌BFE 900的EntB的遗传特征和产生与迄今为止描述的不同,因为存在一个保守序列,如EntB基因上游的调控框,并且其产生是组成性的,而不是受调控的。这个2.2kb的染色体片段含有迄今未检测到的EntB免疫基因,其非典型方向与结构基因的方向相反。在包含EntB结构基因的12.0 kb染色体片段上未检测到典型的转运和与细菌素产生相关的其他基因。这使得EntB遗传系统与大多数其他细菌素系统不同,在其他细菌素系统中,转运和可能的调节基因都聚类了。 EntB由食肉食杆菌(Carnobacterium piscicola)LV17A的专用分泌机制亚克隆和表达。该结构基因通过PCR扩增,与divergicin A信号肽融合,并通过粪肠球菌ATCC 19433中的一般分泌途径表达。

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