Wang Yunsheng, Chen Yincui, Xin Jiankang, Chen Xianjing, Xu Tingyan, He Jiefang, Pan Zhangxu, Zhang Chuanbo
Laboratory of Microbial Resources and Industrial Application, College of Life Sciences, Guizhou Normal University, Guiyang, China.
Front Microbiol. 2023 Jan 26;14:1080743. doi: 10.3389/fmicb.2023.1080743. eCollection 2023.
As an important source of new drug molecules, secondary metabolites (SMs) produced by microorganisms possess important biological activities, such as antibacterial, anti-inflammatory, and hypoglycemic effects. However, the true potential of microbial synthesis of SMs has not been fully elucidated as the SM gene clusters remain silent under laboratory culture conditions. Herein, we evaluated the inhibitory effect of by co-culture of and three species, including , , and . In addition, a non-target approach based on ultra-performance liquid chromatography time-of-flight mass spectrometry (UPLC-TOF-MS) was used to detect differences in extracellular and intracellular metabolites. Notably, the co-culture of and spices significantly improved the inhibitory effect against , with the combination of and showing best performance. Metabolomics data further revealed that the abundant SMs, such as Nummularine B, Lucidenic acid E2, Elatoside G, Aspergillic acid, 4-Hydroxycyclohexylcarboxylic acid, Copaene, and Pipecolic acid were significantly enhanced in co-culture. Intracellularly, the differential metabolites were involved in the metabolism of amino acids, nucleic acids, and glycerophospholipid. Overall, this work demonstrates that the co-culture strategy is beneficial for inducing biosynthesis of active metabolites in and .
作为新药分子的重要来源,微生物产生的次级代谢产物(SMs)具有重要的生物活性,如抗菌、抗炎和降血糖作用。然而,由于SM基因簇在实验室培养条件下保持沉默,微生物合成SMs的真正潜力尚未得到充分阐明。在此,我们通过将[具体菌种1]与三种[具体菌种2]共同培养,包括[菌种2具体名称1]、[菌种2具体名称2]和[菌种2具体名称3],评估了[具体菌种1]的抑制作用。此外,基于超高效液相色谱飞行时间质谱(UPLC-TOF-MS)的非靶向方法用于检测细胞外和细胞内代谢物的差异。值得注意的是,[具体菌种1]与[具体菌种2]的共同培养显著提高了对[目标菌]的抑制作用,其中[具体菌种1]与[具体菌种2具体名称3]的组合表现最佳。代谢组学数据进一步表明,在共同培养中,丰富的SMs,如钱币菌素B、亮氨酸E2、刺囊酸G、曲霉酸、4-羟基环己基羧酸、古巴烯和哌啶酸显著增加。在细胞内,差异代谢物参与氨基酸、核酸和甘油磷脂的代谢。总体而言,这项工作表明共同培养策略有利于诱导[具体菌种1]和[具体菌种2]中活性代谢物的生物合成。