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首页> 外文期刊>FEMS Microbiology Letters >Vibrio vulnificus metalloprotease VvpE has no direct effect on the iron-assimilation from human holotransferrin
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Vibrio vulnificus metalloprotease VvpE has no direct effect on the iron-assimilation from human holotransferrin

机译:创伤弧菌金属蛋白酶VvpE对人全转铁蛋白的铁同化作用没有直接影响

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In order to elucidate the role of Vibrio vulnificus metalloprotease VvpE in the uptake of iron from human transferrin, we constructed a VvpE-deficient mutant and a merozygotic vvpE-transcriptional reporter from the wild type strain MO6-24/O. All three strains were able to grow only in deferrated Heart Infusion broth (DF-HI) with human holotransferrin (HT), but not in DF-HI containing partially iron-saturated transferrin or apotransferrin, without noticeable differences among the strains. All strains consumed most iron in the early growth phase. Both the transcription and extracellular production of VvpE proceeded at undetectable levels when bacterial growth was severely retarded in the DF-HI. When HT or FeCl3 was added to the DF-HI, the retarded bacterial growth was restored and vvpE transcription dramatically increased in the late growth phase, but the extracellular VvpE production was negligible as compared to its transcription. All strains were unable to degrade HT even in normal HI broth containing HT, in which extracellular VvpE activity was remarkably high. The uptake of iron from HT in all strains was consistent with the production of catechol-siderophore rather than hydroxamate-siderophore. Similar results were also observed when clinical isolates from septicemic patients were used. In conclusion, we determined that VvpE was not directly involved in the siderophore-mediated iron-uptake from human transferrin. In addition, the discrepancy between the transcription and extracellular production of VvpE suggests that additional posttranscriptional events are involved in the extracellular production of VvpE. (c) 2005 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
机译:为了阐明创伤弧菌金属蛋白酶VvpE在人类转铁蛋白摄取铁中的作用,我们从野生型MO6-24 / O构建了一个VvpE缺陷型突变体和一个纯合子vvpE转录报告基因。这三种菌株只能在带有人全转铁蛋白(HT)的延缓心脏输液肉汤(DF-HI)中生长,而不能在含有部分铁饱和转铁蛋白或脱辅基铁蛋白的DF-HI中生长,各菌株之间没有明显差异。在生长初期,所有菌株消耗了大部分铁。当细菌生长在DF-HI中严重受阻时,VvpE的转录和细胞外产生均以不可检测的水平进行。当在DF-HI中添加HT或FeCl3时,恢复了延迟的细菌生长,并且在晚期生长阶段vvpE转录显着增加,但是与转录相比,细胞外VvpE的产生可以忽略不计。即使在含有HT的正常HI肉汤中,所有菌株都不能降解HT,在HT培养液中,胞外VvpE活性非常高。在所有菌株中从HT吸收铁与儿茶酚-铁载体而不是异羟肟酸酯-铁载体的产生是一致的。当使用败血症患者的临床分离株时,也观察到相似的结果。总之,我们确定VvpE不直接参与铁转铁介导的人类转铁蛋白的铁摄取。此外,VvpE的转录和细胞外产生之间的差异表明,额外的转录后事件与VvpE的细胞外产生有关。 (c)2005年欧洲微生物学会联合会。由Elsevier B.V.发布。保留所有权利。

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