Institut für Pharmazeutische Biologie, Universität Bonn, Nussallee 6, 53115, Bonn, Germany.
Institut für Mikrobiologie, Eidgenössische Technische Hochschule (ETH) Zürich, Vladimir-Prelog Weg 4, 8093, Zürich, Switzerland.
Angew Chem Int Ed Engl. 2018 Jan 15;57(3):836-840. doi: 10.1002/anie.201707996. Epub 2017 Dec 20.
The cyclic depsipeptide FR900359 (FR), isolated from the tropical plant Ardisia crenata, is a strong and selective inhibitor of Gq proteins, making it an indispensable pharmacological tool to study Gq-related processes, as well as a promising drug candidate. Gq inhibition is a novel mode of action for defense chemicals and crucial for the ecological function of FR, as shown by in vivo experiments in mice, its affinity to insect Gq proteins, and insect toxicity studies. The uncultured endosymbiont of A. crenata was sequenced, revealing the FR nonribosomal peptide synthetase (frs) gene cluster. We here provide a detailed model of FR biosynthesis, supported by in vitro enzymatic and bioinformatic studies, and the novel analogue AC-1, which demonstrates the flexibility of the FR starter condensation domains. Finally, expression of the frs genes in E. coli led to heterologous FR production in a cultivable, bacterial host for the first time.
从热带植物紫金牛(Ardisia crenata)中分离得到的环状二肽 FR900359(FR)强烈且选择性地抑制 Gq 蛋白,使其成为研究 Gq 相关过程不可或缺的药理学工具,同时也是一种很有前途的候选药物。Gq 抑制是防御化学物质的一种新作用模式,对 FR 的生态功能至关重要,这一点在小鼠体内实验、其对昆虫 Gq 蛋白的亲和力以及昆虫毒性研究中得到了证实。紫金牛的未培养内共生体被测序,揭示了 FR 非核糖体肽合成酶(frs)基因簇。我们在此提供了 FR 生物合成的详细模型,该模型得到了体外酶和生物信息学研究以及新型类似物 AC-1 的支持,该类似物证明了 FR 起始缩合结构域的灵活性。最后,frs 基因在大肠杆菌中的表达首次在可培养的细菌宿主中产生了异源 FR。