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鉴定醋杆菌 CCM 3610 中的θ复制质粒 pGR7。

Characterization of the theta replication plasmid pGR7 from Acetobacter aceti CCM 3610.

机构信息

Department of Plant Systems Biology, VIB, Technologiepark 927, 9052 Gent, Belgium.

出版信息

Res Microbiol. 2012 Jul;163(6-7):419-26. doi: 10.1016/j.resmic.2012.07.002. Epub 2012 Jul 24.

Abstract

A cryptic plasmid of Acetobacter aceti CCM 3610, designated pGR7, was sequenced and characterized. It is a 2446-bp circular molecule with a G + C content of 30%, which is unusual when compared to the already known plasmids isolated from Acetobacter genera. Sequence analysis of pGR7 revealed three putative open reading frames (ORFs). ORF1 displays low similarity with other Acetobacter plasmid replication proteins. The other two ORFs show similarities only to hypothetical proteins and do not encode any important protein. The replication module comprises a DnaA box-like sequence, indirect repeats, a potential prokaryotic promoter and the rep gene. The rep module organization is similar to that found in other theta-replicating plasmids from acetic acid bacteria that stably maintain in both Acetobacter and Escherichia coli, with two repeated sequences containing modules. Nevertheless, the pGR7 plasmid could replicate and be stably maintained only in Acetobacter strains and not in E. coli, another uncommon feature of this plasmid. The Rep protein was cloned into the pET30a + expression vector and purified by high-performance liquid chromatography. The helicase activity was determined and the ability of the protein to bind to the plasmid regulation region was confirmed by an electrophoretic mobility shift assay. The plasmid was stable in the Acetobacter cells after cultivation under nonselective conditions. By real-time polymerase chain reaction, the relative copy number of pGR7 was estimated to be seven copies per host chromosome equivalent.

摘要

一株醋杆菌 CCM 3610 的隐秘质粒细胞粒,命名为 pGR7,其序列已被测序并进行了特征描述。它是一个 2446bp 的圆形分子,G+C 含量为 30%,与已经从醋杆菌属中分离出来的质粒相比,这是不寻常的。pGR7 的序列分析揭示了三个可能的开放阅读框(ORF)。ORF1 与其他醋杆菌质粒复制蛋白的相似度较低。另外两个 ORF 仅与假设蛋白具有相似性,不编码任何重要蛋白。复制模块包括一个 DnaA 盒样序列、间接重复序列、一个潜在的原核启动子和 rep 基因。rep 模块的组织类似于在其他稳定存在于醋杆菌和大肠杆菌中的醋酸菌θ复制质粒中发现的组织,包含两个重复序列的模块。然而,pGR7 质粒只能在醋杆菌菌株中复制和稳定维持,而不能在大肠杆菌中复制,这是该质粒的另一个不常见特征。Rep 蛋白被克隆到 pET30a+表达载体中,并通过高效液相色谱法进行纯化。测定了其解旋酶活性,并通过电泳迁移率变动分析证实了该蛋白与质粒调控区的结合能力。质粒在非选择性条件下培养的醋杆菌细胞中稳定存在。通过实时聚合酶链反应,估计 pGR7 的相对拷贝数为每个宿主染色体当量的七个拷贝。

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