Koehnke Jesko, Bent Andrew F, Houssen Wael E, Mann Greg, Jaspars Marcel, Naismith James H
BSRC, North Haugh, The University, St Andrews, KY16 9ST.
Marine Biodiscovery Centre, Department of Chemistry, University of Aberdeen, Meston Walk, Aberdeen, AB24 3UE.
Curr Opin Struct Biol. 2014 Dec;29:112-121. doi: 10.1016/j.sbi.2014.10.006. Epub 2014 Nov 25.
The biosynthetic pathways for patellamide and related natural products have recently been studied by structural biology. These pathways produce molecules that have a complex framework and exhibit a diverse array of activity due to the variability of the amino acids that are found in them. As these molecules are difficult to synthesize chemically, exploitation of their properties has been modest. The patellamide pathway involves amino acid heterocyclization, peptide cleavage, peptide macrocyclization, heterocycle oxidation and epimerization; closely related products are also prenylated. Enzyme activities have been identified for all these transformations except epimerization, which may be spontaneous. This review highlights the recent structural and mechanistic work on amino acid heterocyclization, peptide cleavage and peptide macrocyclization. This work should help in using the enzymes to produce novel analogs of the natural products enabling an exploitation of their properties.
最近,结构生物学对巴特拉胺及相关天然产物的生物合成途径进行了研究。这些途径产生的分子具有复杂的框架结构,并且由于其中所含氨基酸的变异性而展现出多种多样的活性。由于这些分子难以通过化学方法合成,因此对其性质的开发利用程度有限。巴特拉胺途径涉及氨基酸杂环化、肽裂解、肽大环化、杂环氧化和差向异构化;与之密切相关的产物还会发生异戊烯基化。除差向异构化(可能是自发的)外,所有这些转化的酶活性均已得到鉴定。本综述重点介绍了最近在氨基酸杂环化、肽裂解和肽大环化方面的结构和机理研究。这项工作应有助于利用这些酶生产天然产物的新型类似物,从而能够开发利用它们的性质。