Institute of Pharmaceutical Biotechnology & Research Center for Clinical Pharmacy, The First Affiliated Hospital, School of Medicine, Zhejiang University, 310058, Hangzhou, China.
Zhejiang Provincial Key Laboratory for Microbial Biochemistry and Metabolic Engineering, 310058, Hangzhou, China.
Commun Biol. 2020 Apr 24;3(1):192. doi: 10.1038/s42003-020-0924-2.
Due to the plethora natural products made by Streptomyces, the regulation of its metabolism are of great interest, whereas there is a lack of detailed understanding of the role of posttranslational modifications (PTM) beyond traditional transcriptional regulation. Herein with Streptomyces roseosporus as a model, we showed that crotonylation is widespread on key enzymes for various metabolic pathways, and sufficient crotonylation in primary metabolism and timely elimination in secondary metabolism are required for proper Streptomyces metabolism. Particularly, the glucose kinase Glk, a keyplayer of carbon catabolite repression (CCR) regulating bacterial metabolism, is identified reversibly crotonylated by the decrotonylase CobB and the crotonyl-transferase Kct1 to negatively control its activity. Furthermore, crotonylation positively regulates CCR for Streptomyces metabolism through modulation of the ratio of glucose uptake/Glk activity and utilization of carbon sources. Thus, our results revealed a regulatory mechanism that crotonylation globally regulates Streptomyces metabolism at least through positive modulation of CCR.
由于链霉菌产生了大量的天然产物,因此其代谢的调控引起了极大的关注,然而,除了传统的转录调控之外,人们对翻译后修饰(PTM)的作用还缺乏详细的了解。在此,我们以玫瑰色链霉菌(Streptomyces roseosporus)为模型,表明丙二酰化广泛存在于各种代谢途径的关键酶上,初级代谢中需要足够的丙二酰化和次级代谢中及时的消除,才能使链霉菌代谢正常进行。特别是葡萄糖激酶 Glk,作为调节细菌代谢的碳分解代谢物阻遏(CCR)的关键因子,被去丙二酰化酶 CobB 和丙二酰基转移酶 Kct1 可逆地丙二酰化,从而负调控其活性。此外,丙二酰化通过调节葡萄糖摄取/Glk 活性的比值和碳源的利用,正向调控 CCR 以促进链霉菌代谢。因此,我们的研究结果揭示了一种调控机制,即丙二酰化通过正向调控 CCR 来全局调控链霉菌代谢。