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首页> 外文期刊>Applied and Environmental Microbiology >Riboflavin Biosynthesis Is Associated with Assimilatory Ferric Reduction and Iron Acquisition by Campylobacter jejuni
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Riboflavin Biosynthesis Is Associated with Assimilatory Ferric Reduction and Iron Acquisition by Campylobacter jejuni

机译:核黄素的生物合成与空肠弯曲杆菌的拟铁还原和铁的吸收有关

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One of the pathways involved in the acquisition of the essential metal iron by bacteria involves the reduction of insoluble Fe3+ to soluble Fe2+, followed by transport of Fe2+ to the cytoplasm. Flavins have been implicated as electron donors in this poorly understood process. Ferrous iron uptake is essential for intestinal colonization by the important pathogen Campylobacter jejuni and may be of particular importance under low-oxygen conditions. In this study, the links among riboflavin biosynthesis, ferric reduction, and iron acquisition in C. jejuni NCTC11168 have been investigated. A riboflavin auxotroph was generated by inactivation of the ribB riboflavin biosynthesis gene (Cj0572), and the resulting isogenic ribB mutant only grew in the presence of exogenous riboflavin or the riboflavin precursor diacetyl but not in the presence of the downstream products flavin adenine dinucleotide and flavin mononucleotide. Riboflavin uptake was unaffected in the ribB mutant under iron-limited conditions but was lower in both the wild-type strain and the ribB mutant under iron-replete conditions. Mutation of the fur gene, which encodes an iron uptake regulator of C. jejuni, resulted in an increase in riboflavin uptake which was independent of the iron content of the medium, suggesting a role for Fur in the regulation of the as-yet-unknown riboflavin transport system. Finally, ferric reduction activity was independent of iron availability in the growth medium but was lowered in the ribB mutant compared to the wild-type strain and, conversely, increased in the fur mutant. Taken together, the findings confirm close relationships among iron acquisition, riboflavin production, and riboflavin uptake in C. jejuni.
机译:细菌获取必需金属铁的途径之一涉及将不溶性Fe3 +还原为可溶性Fe2 +,然后将Fe2 +转运至细胞质。在这个鲜为人知的过程中,黄素被认为是电子供体。对于重要的病原空肠弯曲菌在肠道中定殖,铁的摄取是必不可少的,在低氧条件下可能尤其重要。在这项研究中,研究了空肠弯曲菌NCTC11168中核黄素生物合成,铁还原和铁获取之间的联系。通过灭活ribB核黄素生物合成基因(Cj0572)产生核黄素营养缺陷型,并且所得等基因ribB突变体仅在外源核黄素或核黄素前体二乙酰存在下生长,而在下游产物黄素腺嘌呤二核苷酸和黄素不存在下生长单核苷酸。在铁受限的条件下,ribB突变体中核黄素的摄取不受影响,但在铁充足的条件下,野生型菌株和ribB突变体中的核黄素摄取均较低。编码空肠弯曲杆菌铁吸收调节剂的fur基因突变导致核黄素吸收增加,而与培养基中铁含量无关,这暗示了Fur在调节迄今未知的过程中的作用核黄素转运系统。最后,还原铁的活性与生长培养基中铁的有效性无关,但与野生型菌株相比,在ribB突变体中降低,而在fur突变体中则增加。综上所述,这些发现证实空肠弯曲杆菌中铁的获取,核黄素的产生和核黄素的摄取之间有着密切的关系。

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