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The kfrA gene is the first in a tricistronic operon required for survival of IncP-1 plasmid R751

机译:KFRA基因是第一个在INCP-1质粒R751存活所需的三函数式操纵子中的第一

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The kfrA gene of the IncP-1 broad-host-range plasmids is the best-studied member of a growing gene family that shows strong linkage to the minimal replicon of many low-copy-number plasmids. KfrA is a DNA binding protein with a long, alpha-helical, coiled-coil tail. Studying IncP-1β plasmid R751, evidence is presented that kfrA and its downstream genes upf54.8 and upf54.4 were organized in a tricistronic operon (renamed here kfrA kfrB kfrC), expressed from autoregulated kfrAp, that was also repressed by KorA and KorB. KfrA, KfrB and KfrC interacted and may have formed a multi-protein complex. Inactivation of either kfrA or kfrB in R751 resulted in long-term accumulation of plasmid-negative bacteria, whereas wild-type R751 itself persisted without selection. Immunofluorescence studies showed that KfrAR751 formed plasmid-associated foci, and deletion of the C terminus of KfrA caused plasmid R751ΔC2kfrA foci to disperse and mislocalize. Thus, the KfrABC complex may be an important component in the organization and control of the plasmid clusters that seem to form the segregating unit in bacterial cells. The studied operon is therefore part of the set of functions needed for R751 to function as an efficient vehicle for maintenance and spread of genes in Gram-negative bacteria.
机译:INCP-1广泛宿主范围质粒的KFRA基因是生长基因家族的最佳研究成员,其表现出对许多低拷贝数质粒的最小复制子的强烈连锁。 KFRA是一种具有长,α-螺旋,卷轴尾部的DNA结合蛋白。研究Incp-1β质粒R751,证据表明,kFRA及其下游基因为UPF54.8和UPF54.4在特定调节KFRAP中表达的三分钟操纵子(重命名KFRA KFRB KFRC),该kfrap表达,也由Kora和Korb抑制。 KFRA,KFRB和KFRC相互作用,可以形成多蛋白质复合物。 R751中KFRA或KFRB的失活导致质粒阴性细菌的长期积累,而野生型R751本身持续无需选择。免疫荧光研究表明,KFRAR751形成了质粒相关的焦点,并且缺失KFRA的C末端引起质粒R751ΔC2KFRA焦点分散和错误定位。因此,KFRABC复合物可以是组织中的重要组成部分和控制似乎在细菌细胞中形成分离单元的质粒簇。因此,研究的操纵子是R751所需的一组功能的一部分,其用作革兰氏阴性细菌中基因的高效载体的功能。

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