Kleinkauf H, von Döhren H
Institute of Biochemistry and Molecular Biology, Technical University Berlin, Germany.
Antonie Van Leeuwenhoek. 1995;67(3):229-42. doi: 10.1007/BF00873687.
A variety of peptides have been detected in microorganisms. Some have found applications in various fields, for example the classical beta-lactam antibiotics, immunosuppressors like cyclosporin, promising new antibacterials like teichoplanin or daptomycin and antifungals like echinocandin. For none of these has it been established how their complicated biosynthetic pathways have evolved or what functions they fulfill within or for their producers. So it is unclear what selection processes limit the range of their structural analogues within various groups of microorganisms. We here consider recent data in the field of biosynthesis and how they may suggest mechanisms of genetic diversity. These may illustrate the complexity of genetic and intracellular organization of biosynthetic pathways and indicate the cellular context of some metabolites related to the complex background of the production of each metabolite. Research focusing on various targets like the increase of productivity of fermentations or the spread of resistances to antibacterials is slowly being understood.
在微生物中已检测到多种肽。其中一些已在各个领域得到应用,例如经典的β-内酰胺抗生素、像环孢素这样的免疫抑制剂、有前景的新型抗菌药物如替考拉宁或达托霉素以及像棘白菌素这样的抗真菌药物。对于这些肽中的任何一种,都尚未确定其复杂的生物合成途径是如何进化的,或者它们在生产者体内或为生产者所发挥的功能是什么。因此,尚不清楚是什么选择过程限制了它们在各种微生物群体中的结构类似物范围。我们在此考虑生物合成领域的最新数据以及它们如何可能暗示遗传多样性的机制。这些可能说明了生物合成途径的遗传和细胞内组织的复杂性,并表明了一些代谢物的细胞背景,这些代谢物与每种代谢物产生的复杂背景相关。专注于各种目标(如提高发酵生产力或抗菌药物耐药性传播)的研究正逐渐被理解。