National Engineering Laboratory for Deep Process of Rice and Byproducts, Hunan Key Laboratory of Grain-oil Deep Process and Quality Control, Hunan Key Laboratory of Processed Food for Special Medical Purpose, College of Food Science and Engineering, Central South University of Forestry and Technology, Changsha, Hunan 41004, China.
National Engineering Laboratory for Deep Process of Rice and Byproducts, Hunan Key Laboratory of Grain-oil Deep Process and Quality Control, Hunan Key Laboratory of Processed Food for Special Medical Purpose, College of Food Science and Engineering, Central South University of Forestry and Technology, Changsha, Hunan 41004, China.
J Biotechnol. 2021 Nov 20;341:137-145. doi: 10.1016/j.jbiotec.2021.09.018. Epub 2021 Oct 1.
Extractive fermentation has been proven to be efficient in enhancing the secretion and production of secondary metabolites in submerged fermentation by Monascus spp., owing to increased cell membrane permeability and resolved product inhibition. In this study, we investigated the regulation effect of Triton X-100 on cell growth and secondary metabolite biosynthesis in submerged fermentation of M. purpureus DK. The results show that the maximum monascus pigments (MPs), citrinin (CIT) production, and specific growth rate are 136.86 U/mL, 4.57 mg/L, and 0.04 h, respectively, when 3 g/L of Triton X-100 is supplemented after fermentation for 10 d, and the extracellular MPs and CIT increased by 127.48% and 288.57%, respectively. RT-qPCR shows that the expression levels of MPs and CIT biosynthesis gene clusters are significantly upregulated, whereas those of glycolysis, tricarboxylic acid cycle, respiratory chains, and ATP synthase are downregulated. This study provides a vital strategy for extractive fermentation under extreme environmental conditions for further enhancing MP production.
萃取发酵已被证明在增加红曲属菌属的次级代谢产物分泌和生产方面非常有效,这归因于增加的细胞膜通透性和解决的产物抑制。在这项研究中,我们研究了 Triton X-100 对米曲霉菌 DK 浸式发酵中细胞生长和次级代谢产物生物合成的调节作用。结果表明,当在发酵 10 天后补加 3 g/L 的 Triton X-100 时,最大的红曲色素(MPs)、桔霉素(CIT)产量和比生长速率分别为 136.86 U/mL、4.57 mg/L 和 0.04 h,并且胞外 MPs 和 CIT 分别增加了 127.48%和 288.57%。RT-qPCR 显示 MPs 和 CIT 生物合成基因簇的表达水平显著上调,而糖酵解、三羧酸循环、呼吸链和 ATP 合酶的表达水平则下调。这项研究为在极端环境条件下进行萃取发酵提供了重要策略,以进一步提高 MPs 的产量。