Kopp Florian, Mahlert Christoph, Grünewald Jan, Marahiel Mohamed A
Fachbereich Chemie/Biochemie, Philipps-Universität Marburg, Hans-Meerwein-Strasse, 35043 Marburg, Germany.
J Am Chem Soc. 2006 Dec 27;128(51):16478-9. doi: 10.1021/ja0667458.
Many biologically active natural products have macrocyclic structures. In nonribosomal peptides macrocyclization is commonly achieved via the formation of intramolecular ester or amide bond catalyzed by thioesterase domains during biosynthesis. A unique and so far unknown type of peptide cyclization occurs in the nostocyclopeptide, a macrocyclic imine produced by the terrestrial cyanobacterium Nostoc sp. ATCC53789. In this work we show that a C-terminal reductase domain of the nostocyclopeptide nonribosomal peptide synthetase catalyzes the reductive release of a linear peptide aldehyde and thereby triggers the spontaneous formation of a stable imino head-to-tail linkage. This type of molecular self-assembly induced by the reductive release of reactive aldehydes may be more commonplace in other complex nonribosomal peptides than originally thought.
许多具有生物活性的天然产物都具有大环结构。在非核糖体肽中,大环化通常是在生物合成过程中通过硫酯酶结构域催化形成分子内酯键或酰胺键来实现的。一种独特且迄今未知的肽环化类型发生在 nostocyclopeptide 中,nostocyclopeptide 是一种由陆生蓝藻 Nostoc sp. ATCC53789 产生的大环亚胺。在这项工作中,我们表明 nostocyclopeptide 非核糖体肽合成酶的 C 末端还原酶结构域催化线性肽醛的还原释放,从而触发稳定的亚氨基头对尾连接的自发形成。由反应性醛的还原释放诱导的这种分子自组装类型在其他复杂的非核糖体肽中可能比最初认为的更为常见。