Panthee Suresh, Hamamoto Hiroshi, Paudel Atmika, Sekimizu Kazuhisa
Teikyo University Institute of Medical Mycology, 359 Otsuka, Hachioji, Tokyo, 192-0395, Japan.
Laboratory of Microbiology, Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan.
Arch Microbiol. 2016 Nov;198(9):839-45. doi: 10.1007/s00203-016-1278-5. Epub 2016 Aug 19.
Infectious diseases threaten global health due to the ability of microbes to acquire resistance against clinically used antibiotics. Continuous discovery of antibiotics with a novel mode of action is thus required. Actinomycetes and fungi are currently the major sources of antibiotics, but the decreasing rate of discovery of novel antibiotics suggests that the focus should be changed to previously untapped groups of microbes. Lysobacter species have a genome size of ~6 Mb with a relatively high G + C content of 61-70 % and are characterized by their ability to produce peptides that damage the cell walls or membranes of other microbes. Genome sequence analysis revealed that each Lysobacter species has gene clusters for the production of 12-16 secondary metabolites, most of which are peptides, thus making them 'peptide production specialists'. Given that the number of antibiotics isolated is much lower than the number of gene clusters harbored, further intensive studies of Lysobacter are likely to unearth novel antibiotics with profound biomedical applications. In this review, we summarize the structural diversity, activity and biosynthesis of lysobacterial antibiotics and highlight the importance of Lysobacter species for antibiotic production.
由于微生物能够获得对临床使用抗生素的抗性,传染病对全球健康构成威胁。因此,需要持续发现具有新作用模式的抗生素。放线菌和真菌目前是抗生素的主要来源,但新型抗生素的发现率不断下降,这表明应将重点转向以前未开发的微生物群体。溶杆菌属物种的基因组大小约为6 Mb,G + C含量相对较高,为61-70%,其特点是能够产生破坏其他微生物细胞壁或细胞膜的肽。基因组序列分析表明,每个溶杆菌属物种都有用于生产12-16种次级代谢产物的基因簇,其中大多数是肽,因此使它们成为“肽生产专家”。鉴于分离出的抗生素数量远低于所拥有的基因簇数量,对溶杆菌属进行进一步深入研究可能会发掘出具有重要生物医学应用的新型抗生素。在这篇综述中,我们总结了溶杆菌属抗生素的结构多样性、活性和生物合成,并强调了溶杆菌属物种在抗生素生产中的重要性。