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Complete sequence of the enterocin Q-encoding plasmid pCIZ2 from the multiple bacteriocin producer Enterococcus faecium L50 and genetic characterization of enterocin Q production and immunity.

机译:来自多个细菌素生产者粪肠球菌L50的肠球菌Q编码质粒pCIZ2的完整序列,以及肠球菌Q产生和免疫的遗传学特征。

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摘要

The locations of the genetic determinants for enterocin L50 (EntL50A and EntL50B), enterocin Q (EntQ), and enterocin P (EntP) in the multiple bacteriocin producer Enterococcus faecium strain L50 were determined. These bacteriocin genes occur at different locations; entL50AB (encoding EntL50A and EntL50B) are on the 50-kb plasmid pCIZ1, entqA (encoding EntQ) is on the 7.4-kb plasmid pCIZ2, and entP (encoding EntP) is on the chromosome. The complete nucleotide sequence of pCIZ2 was determined to be 7,383 bp long and contains 10 putative open reading frames (ORFs) organized in three distinct regions. The first region contains three ORFs: entqA preceded by two divergently oriented genes, entqB and entqC. EntqB shows high levels of similarity to bacterial ATP-binding cassette (ABC) transporters, while EntqC displays no significant similarity to any known protein. The second region encompasses four ORFs (orf4 to orf7), and ORF4 and ORF5 display high levels of similarity to mobilization proteins from E. faecium and Enterococcus faecalis. In addition, features resembling a transfer origin region (oriT) were found in the promoter area of orf4. The third region contains three ORFs (orf8 to orf10), and ORF8 and ORF9 exhibit similarity to the replication initiator protein RepE from E. faecalis and to RepB proteins, respectively. To clarify the minimum requirement for EntQ synthesis, we subcloned and heterologously expressed a 2,371-bp fragment from pCIZ2 that encompasses only the entqA, entqB, and entqC genes in Lactobacillus sakei, and we demonstrated that this fragment is sufficient for EntQ production. Moreover, we also obtained experimental results indicating that EntqB is involved in ABC transporter-mediated EntQ secretion, while EntqC confers immunity to this bacteriocin.
机译:确定了肠球菌L50(EntL50A和EntL50B),肠球菌素Q(EntQ)和肠球菌素P(EntP)的遗传决定因素在多重细菌素生产者粪肠球菌L50菌株中的位置。这些细菌素基因出现在不同的位置。 entL50AB(编码EntL50A和EntL50B)在50 kb质粒pCIZ1上,entqA(编码EntQ)在7.4kb质粒pCIZ2上,entP(编码EntP)在染色体上。经测定,pCIZ2的完整核苷酸序列长为7,383 bp,包含10个在三个不同区域组织的推定开放阅读框(ORF)。第一个区域包含三个ORF:entqA,后跟两个不同的定向基因entqB和entqC。 EntqB与细菌ATP结合盒(ABC)转运蛋白显示出高水平的相似性,而EntqC与任何已知蛋白均无显着相似性。第二个区域包含四个ORF(orf4至orf7),并且ORF4和ORF5与粪肠球菌和粪肠球菌的动员蛋白具有高度相似性。此外,在orf4的启动子区域发现了类似转移起点区域(oriT)的特征。第三区域包含三个ORF(orf8至orf10),并且ORF8和ORF9分别与粪肠球菌的复制起始蛋白RepE和RepB蛋白相似。为了阐明EntQ合成的最低要求,我们从pCIZ2亚克隆并异源表达了一个2,371 bp的片段,该片段仅包含日本乳杆菌中的entqA,entqB和entqC基因,并且我们证明了该片段足以用于EntQ的生产。此外,我们还获得了表明EntqB参与ABC转运蛋白介导的EntQ分泌的实验结果,而EntqC赋予了对该细菌素的免疫力。

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