Huang Wei, Jiao Xingzhi, Hua Lingqi, Kang Qianjin, Zhang Lili, Luo Xiaoxia, Bai Linquan
College of Life Science and Technology & Xinjiang Production & Construction Corps Key Laboratory of Protection and Utilization of Biological Resources in Tarim Basin, Tarim University, Alar, 843300, Xinjiang, People's Republic of China.
State Key Laboratory of Microbial Metabolism, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, 200240, Shanghai, People's Republic of China.
Synth Syst Biotechnol. 2024 Nov 8;10(1):262-270. doi: 10.1016/j.synbio.2024.11.002. eCollection 2025.
Natural products (NPs) afforded by living-beings, especially by microscopic species, represent invaluable and indispensable reservoirs for drug leads in clinical practice. With the rapid advancement in sequencing technology and bioinformatics, the ever-increasing number of microbial biosynthetic gene clusters (BGCs) were decrypted, while a great deal of BGCs remain cryptic or inactive under standard laboratory culture conditions. Addressing this dilemma requires innovative tactics to awaken quiescence of BGCs by releasing the potential of microbial secondary metabolism for mining novel NPs. In this study, a universal strategy was proposed to induce the expression of silent BGCs by leveraging the dynamic interactions among coexisting microbial neighbors within a microbiota. This approach involves the deconstruction/reconstruction of binary interactions among the coexisting neighbors to create a pipeline for BGCs arousing. Coupled with the acquisition of 2760 microbial individuals from the (Luobuma, LBM) phyllosphere in a successive dilution procedure, 44 culturable isolates were screened using binary interaction, in which 12.6 % pairs demonstrated potent mutual interacting effects. Furthermore, after selecting the four most promising isolates, a full-scale metabolic inspection was conducted, in which 25.3 % of the interacting pairs showcased significant metabolomic variations with de-cryptic activities. Notably, with the aid of visualization of IMS technology, one of the physiologically functional entities, the bactericidal agent resistomycin, was elucidated from the core interacting pair between the co-culture of the sp. LBM_605 and the sp. LBM_791. This study highlights the intrinsic interactions among coexisting microorganisms within a phyllosphere microbiota as novel avenues for exploring and harnessing NPs.
生物,特别是微观物种所产生的天然产物(NPs),是临床实践中药物先导物的宝贵且不可或缺的来源。随着测序技术和生物信息学的快速发展,越来越多的微生物生物合成基因簇(BGCs)被解密,然而在标准实验室培养条件下,仍有大量BGCs处于隐秘或无活性状态。解决这一困境需要创新策略,通过释放微生物次级代谢潜力来挖掘新型NPs,从而唤醒BGCs的静止状态。在本研究中,提出了一种通用策略,即利用微生物群落中共存的微生物邻居之间的动态相互作用来诱导沉默BGCs的表达。该方法涉及解构/重建共存邻居之间的二元相互作用,以创建一条唤醒BGCs的途径。通过连续稀释程序从罗布麻(Luobuma,LBM)叶际采集了2760个微生物个体,利用二元相互作用筛选出44株可培养分离株,其中12.6%的配对表现出强大的相互作用效果。此外,在选择了四个最有前景的分离株后,进行了全面的代谢检查,其中25.3%的相互作用配对表现出具有解密活性的显著代谢组学变化。值得注意的是,借助IMS技术的可视化,从LBM_605菌株和LBM_791菌株共培养的核心相互作用对中阐明了一种生理功能实体——杀菌抗生素抗霉素。本研究强调了叶际微生物群落中共存微生物之间的内在相互作用,是探索和利用NPs的新途径。