Yan Xiaoli, Zhang Benyin, Tian Wenya, Dai Qi, Zheng Xiaoqin, Hu Ke, Liu Xinxin, Deng Zixin, Qu Xudong
Key Laboratory of Combinatorial Biosynthesis and Drug Discovery Ministry of Education, School of Pharmaceutical Sciences, Wuhan University, China.
State Key Laboratory of Plateau Ecology and Agriculture, Qinghai University, China.
Synth Syst Biotechnol. 2018 Feb 12;3(1):76-80. doi: 10.1016/j.synbio.2018.02.001. eCollection 2018 Mar.
Natural product discovery is pivot for drug development, however, this endeavor is often challenged by the wide inactivation or silence of natural products biosynthetic pathways. We recently developed a highly efficient approach to activate cryptic/silenced biosynthetic pathways through augmentation of the phosphopantetheinylation of carrier proteins. By applying this approach in the NRRL B-1832, we herein identified three cryptic nucleosides products, including one known puromycin A and two new derivatives (puromycin B and C). The biosynthesis of these products doesn't require the involvement of carrier protein, indicating the phosphopantetheinyl transferase (PPtase) indeed plays a fundamental regulatory role in metabolites biosynthesis. These results demonstrate that the PPtase-based approach have a much broader effective scope than the previously assumed carrier protein-involving pathways, which will benefit future natural products discovery and biosynthetic studies.
天然产物的发现是药物开发的关键,然而,这一努力常常受到天然产物生物合成途径广泛失活或沉默的挑战。我们最近开发了一种高效的方法,通过增强载体蛋白的磷酸泛酰巯基乙胺化来激活隐秘/沉默的生物合成途径。通过在NRRL B - 1832中应用这种方法,我们在此鉴定出三种隐秘核苷产物,包括一种已知的嘌呤霉素A和两种新衍生物(嘌呤霉素B和C)。这些产物的生物合成不需要载体蛋白的参与,这表明磷酸泛酰巯基乙胺基转移酶(PPtase)确实在代谢物生物合成中发挥着基本的调节作用。这些结果表明,基于PPtase的方法比之前假定的涉及载体蛋白的途径具有更广泛的有效范围,这将有利于未来天然产物的发现和生物合成研究。