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首页> 外文期刊>Journal of bacteriology >A Genomic Islet Mediates Flagellar Phase Variation in Escherichia coli Strains Carrying the Flagellin-Specifying Locus flk
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A Genomic Islet Mediates Flagellar Phase Variation in Escherichia coli Strains Carrying the Flagellin-Specifying Locus flk

机译:基因组胰岛介导携带鞭毛蛋白特异性基因座flk的大肠杆菌菌株鞭毛相变

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The occurrence of unilateral flagellar phase variation was previously demonstrated in Escherichia coli strains carrying the non-fliC flagellin-specifying locus flk. In this study, we investigated the mechanism involved in this process. By using sequencing and sequence analysis, the flk region between the chromosomal genes yhaC and rnpB was characterized in all described flk-positive E. coli strains, including the H35 strain identified in this study (the other strains used are H3, H36, H47, and H53 strains), and this region was found to contain a putative integrase gene and flanking direct repeats in addition to the flk flagellin-specifying gene flkA and a fliC repressor gene, flkB, indicating that there is a typical genomic islet (GI), which was designated the flk GI. The horizontal transfer potential of the flk GI was indicated by detection of the excised extrachromosomal circular form of the flk GI. By generating fliC-expressing variants of H3 and H47 strains, unilateral flagellar phase variation in flk-positive strains was shown to be mediated by excision of the flk GI. The function of the proposed integrase gene was confirmed by deletion and a complementation test. The potential integration sites of the flk GI were identified. A general model for flagellar phase variation in flk-positive E. coli strains can be expressed as fliCoff + flkAon → fliCon + flkAnone. This is the first time that a molecular mechanism for flagellar phase variation has been reported for E. coli.
机译:先前已在携带非 fliC 鞭毛蛋白特异性基因座 flk 大肠杆菌菌株中证实了单侧鞭毛相变的发生。在这项研究中,我们调查了此过程涉及的机制。通过测序和序列分析,在所有描述的 flk 中表征了染色体基因 yhaC rnpB 之间的 flk 区>阳性 E。大肠杆菌菌株,包括在本研究中鉴定的H35菌株(使用的其他菌株是H3,H36,H47和H53菌株),发现该区域还包含推定的整合酶基因,并且除了侧翼外,还存在直接重复序列 flk 鞭毛蛋白特异性基因 flkA fliC 阻遏基因 flkB ,表明存在典型的基因组胰岛(GI),称为 flk GI。通过检测切下的 flk GI的染色体外圆形形式表明 flk GI的水平转移潜力。通过产生表达H3和H47菌株的 fliC 变体,表明 flk 阳性菌株的单侧鞭毛相变是通过切除 flk 介导的。 em> GI。通过缺失和互补测试证实了所提出的整合酶基因的功能。确定了 flk GI的潜在整合位点。 flk -阳性 E中鞭毛相变的一般模型。大肠杆菌可以表示为 fliC off + flkA on fliC on + flkA none 。这是首次报道了 E鞭毛相变的分子机制。大肠杆菌

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