Mady Ahmed S A, Zolova Olga E, Millán María Álvarez San, Villamizar Germán, de la Calle Fernando, Lombó Felipe, Garneau-Tsodikova Sylvie
University of Michigan, Life Sciences Institute, 210 Washtenaw Ave, Ann Arbor, MI 48109, USA.
Mol Biosyst. 2011 Jun;7(6):1999-2011. doi: 10.1039/c1mb05044c. Epub 2011 Apr 11.
An antitumor agent thiocoraline is a thiodepsipeptide marine product derived from two Micromonospora sp. strains that inhibits protein synthesis by binding of its key 3-hydroxyquinaldic acid (3HQA) chromophores to duplex DNA. There are at least two potential pathways via which the 3HQA moiety could be biosynthesized from L-Trp. By biochemical characterization and by preparation of knockouts of an adenylation-thiolation enzyme, TioK, and of two type II thioesterases, TioP and TioQ, found in the thiocoraline biosynthetic gene cluster, we gained valuable insight into the pathway followed for the production of 3HQA.
抗肿瘤药物硫代珊瑚菌素是一种硫代缩肽类海洋产物,源自两种小单孢菌属菌株,它通过其关键的3-羟基喹哪啶酸(3HQA)发色团与双链DNA结合来抑制蛋白质合成。从L-色氨酸生物合成3HQA部分至少有两条潜在途径。通过生物化学特性分析以及制备硫代珊瑚菌素生物合成基因簇中发现的腺苷酸化-硫醇化酶TioK、两种II型硫酯酶TioP和TioQ的基因敲除菌株,我们对3HQA的产生途径有了宝贵的认识。