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Inactivation of the virulence factors from 2,3-butanediol-producing Klebsiella pneumoniae

机译:灭活产生2,3-丁二醇的肺炎克雷伯菌的致病因子

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The microbiological production of 2,3-butanediol (2,3-BDO) has attracted considerable attention as an alternative way to produce high-value chemicals from renewable sources. Among the number of 2,3-BDO-producing microorganisms, Klebsiella pneumoniae has been studied most extensively and is known to produce large quantity of 2,3-BDO from a range of substrates. On the other hand, the pathogenic characteristics of the bacteria have limited its industrial applications. In this study, two major virulence traits, outer core LPS and fimbriae, were removed through homologous recombination from 2,3-BDO-producing K. pneumoniae 2242 to expand its uses to the industrial scale. The K. pneumoniae 2242 a dagger wabG mutant strain was found to have an impaired capsule, which significantly reduced its ability to bind to the mucous layer and evade the phagocytic activity of macrophage. The association with the human ileocecal epithelial cell, HCT-8, and the bladder epithelial cell, T-24, was also reduced dramatically in the K. pneumoniae 2242 a dagger fimA mutant strain that was devoid of fimbriae. However, the growth rate and production yield for 2,3-BDO were unaffected. The K. pneumoniae strains developed in this study, which are devoid of the major virulence factors, have a high potential for the efficient and sustainable production of 2,3-BDO.
机译:2,3-丁二醇(2,3-BDO)的微生物生产作为一种可再生来源生产高价值化学品的替代方法引起了广泛关注。在产生2,3-BDO的多种微生物中,肺炎克雷伯氏菌得到了最广泛的研究,已知可以从多种底物中产生大量2,3-BDO。另一方面,细菌的致病特性限制了其工业应用。在这项研究中,通过同源重组从产生2,3-BDO的肺炎克雷伯菌2242中去除了两个主要的毒力特性,即外核LPS和菌毛,从而将其用途扩大到工业规模。发现肺炎克雷伯菌2242匕首wabG突变株的胶囊受损,这大大降低了其与粘液层结合的能力并逃避了巨噬细胞的吞噬活性。与人回盲肠上皮细胞HCT-8和膀胱上皮细胞T-24的关联在肺炎克雷伯菌2242缺失纤维菌的匕首fimA突变株中也显着降低。但是,2,3-BDO的增长率和产量不受影响。这项研究中开发的肺炎克雷伯氏菌菌株没有主要毒力因子,具有高效和可持续生产2,3-BDO的巨大潜力。

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