Narayan Radha S, Vannieuwenhze Michael S
Department of Chemistry and Biochemistry, University of California, San Diego, USA.
European J Org Chem. 2007 Jan 19;2007(9):1399-1414. doi: 10.1002/ejoc.200600750.
Several widely used antibiotics such as beta-lactams, glycopeptides, and lipoglycopeptides exhibit their activity by interfering with peptidoglycan biosynthesis. Ever-increasing resistance to these and other agents has placed a renewed emphasis on the need to understand the reactions in this bio-synthetic pathway at the molecular level. While efficient access to many of the biosynthetic enzymes has been gained, the isolation of their natural substrates has proven difficult. Chemical synthesis has provided valuable tools to circumvent this problem and has allowed convenient access to several key intermediates and analogs thereof. Recent advances in the synthesis of the late-stage intermediates, including the Park nucleotide, lipid I, lipid II, fragments of the bacterial cell wall, along with other biochemical probes are reviewed. A brief discussion on the use of these substrates in study of this important biosynthetic pathway is also included.
几种广泛使用的抗生素,如β-内酰胺类、糖肽类和脂糖肽类,通过干扰肽聚糖生物合成来发挥其活性。对这些及其他药物的耐药性不断增加,再次强调了在分子水平上理解这一生物合成途径中反应的必要性。虽然已经能够有效获取许多生物合成酶,但事实证明,分离它们的天然底物很困难。化学合成提供了有价值的工具来规避这一问题,并使得能够方便地获取几种关键中间体及其类似物。本文综述了后期中间体合成方面的最新进展,包括帕克核苷酸、脂质I、脂质II、细菌细胞壁片段以及其他生化探针。还简要讨论了这些底物在研究这一重要生物合成途径中的应用。