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从海盗和杀手:代谢物多样性是否驱动细菌竞争?

From pirates and killers: does metabolite diversity drive bacterial competition?

机构信息

Department of Chemistry, Konstanz Research School Chemical Biology, University of Konstanz, 78457 Konstanz, Germany.

出版信息

Org Biomol Chem. 2018 Apr 25;16(16):2814-2819. doi: 10.1039/c8ob00150b.

Abstract

Bacteria engage in numerous collaborative and competitive interactions, which are often mediated by small molecule metabolites. Bacterial competition involves for example the production of compounds that effectively kill or inhibit growth of their neighbours but also the secretion of siderophores that allow securing the essential and fiercely embattled resource of ferric iron. Yet, the enormous diversity of metabolites produced has remained puzzling in many cases. We here present examples of both types of competition from our recent work. These include the human pathogen Pseudomonas aeruginosa producing HQNO derived 4-quinolone N-oxides varying in chain length and saturation as antibiotics against Staphylococcus aureus and two marine bacteria, Shewanella algae and Vibrio alginolyticus competing for iron acquisition via homodimeric and heterodimeric cyclic hydroxamate siderophores. In each case, bacteria not only produce one but a whole set of closely related metabolites encoded by a single biosynthetic gene cluster. Our recent work has demonstrated that individual metabolites can have significantly different biological activities and we speculate on the reasons for maintaining this metabolite diversity from the perspective of interspecies competition.

摘要

细菌之间存在着大量的合作和竞争相互作用,这些相互作用通常由小分子代谢物介导。例如,细菌竞争涉及到产生有效杀死或抑制其邻居生长的化合物,以及分泌铁载体来获取铁这种必不可少且竞争激烈的资源。然而,在许多情况下,产生的代谢物的巨大多样性仍然令人费解。我们在这里从最近的工作中举了两个竞争类型的例子。其中包括人类病原体铜绿假单胞菌产生的 HQNO 衍生的 4-喹诺酮 N-氧化物,其链长和饱和度不同,可作为抗生素对抗金黄色葡萄球菌,以及两种海洋细菌,希瓦氏菌和弧菌,通过同二聚体和异二聚体环状羟肟酸铁载体竞争铁的获取。在每种情况下,细菌不仅产生一种,而是一整套由单个生物合成基因簇编码的密切相关的代谢物。我们最近的工作表明,单个代谢物可能具有显著不同的生物学活性,我们从种间竞争的角度推测维持这种代谢物多样性的原因。

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