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Cloning and characterization of the iron uptake gene iutA from avian Escherichia coli

机译:禽大肠杆菌铁摄取基因iutA的克隆与鉴定

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The aim of this work was to isolate, clone and characterize the iron uptake gene iutA from avian pathogenic E. coli ( APEC). The iutA gene was isolated from the strain APEC 9, serotype O2:H9, which was cloned in the expression vector pET101/D-TOPO. The gene of 2.2 Kb was sequenced (AY602767, which showed high similarity to the iutA gene from three plasmids, two from APEC, pAPEC-02-ColV (AY545598.4) and pTJ100 (AY553855.1), and one from a human invasive E. coli strain, the pColV K30. The recombinant protein IutA was over expressed in E. coli BL21(DE-3) and was solubilized with urea and purified by Ni-NTA column. This method produced a relatively high yield of r-IutA of approximately 74kDa, which was used to produce the antibody anti-IutA. This anti-IutA reacted with the protein r-IutA and native IutA of APEC 9, as demonstrated by Western blot, showing that the r-IutA conserved epitopes and its antigenicity was preserved. The anti-IutA IgY was able to inhibit the IutA biological activity, inhibiting the sensitivity to cloacin DF13 of APEC9. However, it did not inhibit the growth of APEC9 in M9 and did not protect the chickens inoculated with the APEC, suggesting that the APEC possessed another iron acquisition mechanism distinct of aerobactin.
机译:这项工作的目的是从禽病原性大肠杆菌(APEC)中分离,克隆和鉴定铁吸收基因iutA。从菌株APEC 9,血清型O2:H9中分离了iutA基因,将其克隆到表达载体pET101 / D-TOPO中。对2.2 Kb的基因进行了测序(AY602767,它与来自三个质粒的iutA基因具有高度相似性,其中两个来自APEC,pAPEC-02-ColV(AY545598.4)和pTJ100(AY553855.1),另一个来自人侵袭性大肠杆菌pColV K30,重组蛋白IutA在大肠杆菌BL21(DE-3)中过表达,用尿素增溶并用Ni-NTA柱纯化​​,该方法产生的r-IutA产量较高大约74kDa的片段被用于产生抗IutA抗体,该抗IutA与APEC 9的r-IutA蛋白和天然IutA反应,如Western blot所示,表明r-IutA保守了表位及其抗原性抗IutA IgY能够抑制IutA的生物学活性,抑制APEC9对cloacin DF13的敏感性,但是,它并没有抑制APEC9在M9中的生长,也没有保护接种APEC的鸡。亚太经合组织拥有另一种铁捕获机制,其独特之处在于航空杆菌素。

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