Sun Yu, Shi Xuan, He Liang-Yu, Xing Yan, Guo Qin-Feng, Xiu Zhi-Long, Dong Yue-Sheng
School of Bioengineering, Dalian University of Technology, Dalian, 116024, Liaoning, China.
Microb Ecol. 2023 May;85(4):1288-1299. doi: 10.1007/s00248-022-02029-1. Epub 2022 May 6.
Microbial co-culture simulates the natural ecosystem through the combination of artificial microbes. This approach has been widely applied in the study of activating silent genes to reveal novel secondary metabolites. However, there are still challenges in determining the biosynthetic pathways. In this study, the effects of microbial co-culture on the morphology of the microbes were verified by the morphological observation. Subsequently, through the strategy combining substrate feeding, stable isotope labeling, and gene expression analysis, the biosynthetic pathways of five benzoic acid derivatives N1-N4 and N7 were demonstrated: the secondary metabolite 10-deoxygerfelin of A. sydowii acted as an inducer to induce B. subtilis to produce benzoic acid, which was further converted into 3-OH-benzoic acid by A. sydowii. Subsequently, A. sydowii used 3-OH-benzoic acid as the substrate to synthesize the new compound N2, and then N1, N3, N4, and N7 were biosynthesized upon the upregulation of hydrolase, hydroxylase, and acyltransferase during co-culture. The plate zone analysis suggested that the biosynthesis of the newly induced compounds N1-N4 was mainly attributed to A. sydowii, and both A. sydowii and B. subtilis were indispensable for the biosynthesis of N7. This study provides an important basis for a better understanding of the interactions among microorganisms, providing new ideas for studying the biosynthetic pathways of the newly induced secondary metabolites in co-culture.
微生物共培养通过人工组合微生物来模拟自然生态系统。这种方法已广泛应用于激活沉默基因以揭示新型次生代谢产物的研究中。然而,在确定生物合成途径方面仍存在挑战。在本研究中,通过形态学观察验证了微生物共培养对微生物形态的影响。随后,通过底物投喂、稳定同位素标记和基因表达分析相结合的策略,证明了五种苯甲酸衍生物N1-N4和N7的生物合成途径:青霉的次生代谢产物10-脱氧格费林作为诱导剂诱导枯草芽孢杆菌产生苯甲酸,青霉再将其进一步转化为3-羟基苯甲酸。随后,青霉以3-羟基苯甲酸为底物合成新化合物N2,然后在共培养过程中,随着水解酶、羟化酶和酰基转移酶的上调,生物合成了N1、N3、N4和N7。平板区域分析表明,新诱导化合物N1-N4的生物合成主要归因于青霉,而N7的生物合成则离不开青霉和枯草芽孢杆菌。本研究为更好地理解微生物之间的相互作用提供了重要依据,为研究共培养中新诱导次生代谢产物的生物合成途径提供了新思路。