Plant Pharmacology Laboratory, Department of Biosystems and Biotechnology, College of Life Science and Biotechnology, Korea University, Seoul 136-713, Korea.
Plant Pathol J. 2015 Mar;31(1):1-11. doi: 10.5423/PPJ.RW.08.2014.0074. Epub 2015 Mar 31.
Antimicrobial cyclic peptides derived from microbes bind stably with target sites, have a tolerance to hydrolysis by proteases, and a favorable degradability under field conditions, which make them an attractive proposition for use as agricultural fungicides. Antimicrobial cyclic peptides are classified according to the types of bonds within the ring structure; homodetic, heterodetic, and complex cyclic peptides, which in turn reflect diverse physicochemical features. Most antimicrobial cyclic peptides affect the integrity of the cell envelope. This is achieved through direct interaction with the cell membrane or disturbance of the cell wall and membrane component biosynthesis such as chitin, glucan, and sphingolipid. These are specific and selective targets providing reliable activity and safety for non-target organisms. Synthetic cyclic peptides produced through combinatorial chemistry offer an alternative approach to develop antimicrobials for agricultural uses. Those synthesized so far have been studied for antibacterial activity, however, the recent advancements in powerful technologies now promise to provide novel antimicrobial cyclic peptides that are yet to be discovered from natural resources.
来源于微生物的抗菌环肽与靶标位点稳定结合,对蛋白酶的水解具有耐受性,并且在野外条件下具有良好的可降解性,这使得它们成为农用杀菌剂的一个有吸引力的选择。抗菌环肽根据环结构内的键的类型进行分类;同二肽、异二肽和复合环肽,这反过来又反映了不同的物理化学特征。大多数抗菌环肽影响细胞包膜的完整性。这是通过与细胞膜直接相互作用或干扰细胞壁和膜成分生物合成来实现的,如几丁质、葡聚糖和鞘脂。这些是特异性和选择性的靶标,为非靶标生物提供可靠的活性和安全性。通过组合化学合成的环肽为开发农用抗菌剂提供了一种替代方法。到目前为止,已经研究了这些合成的环肽的抗菌活性,然而,目前强大技术的最新进展有望提供新的抗菌环肽,这些环肽有待从自然资源中发现。