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温度升高刺激红曲霉CGMCC10910中水溶性荧光黄色色素的生物合成及基因表达。

Rising temperature stimulates the biosynthesis of water-soluble fluorescent yellow pigments and gene expression in Monascus ruber CGMCC10910.

作者信息

Huang Tao, Tan Hailing, Chen Gong, Wang Lu, Wu Zhenqiang

机构信息

School of Bioscience and Bioengineering, Guangdong Provincial Key Laboratory of Fermentation and Enzyme Engineering, South China University of Technology, Guangzhou, 510006, People's Republic of China.

出版信息

AMB Express. 2017 Dec;7(1):134. doi: 10.1186/s13568-017-0441-y. Epub 2017 Jun 24.

Abstract

Monascus species can produce secondary metabolites that have a polyketide structure. In this study, four types of extracellular water-soluble yellow pigments (Y1-Y4) were generated by submerged fermentation with Monascus ruber CGMCC 10910, of which Y3 and Y4 had strong yellow fluorescence. The composition of the pigment mixtures was closely related to the fermentation temperature. The dominating pigments changed from Y1 to Y3 and Y4 when fermentation temperature increased from 30 to 35 °C. Increasing the temperature to 35 °C changed the metabolic pathways of the pigments, which inhibited the biosynthesis of Y1 and enhanced the biosynthesis of Y3 and Y4. Moreover, the yield of Y1 reduced insignificantly, while the yields of Y3 and Y4 increased by 98.21 and 79.31% respectively under two-stage temperature fermentation condition. The expression levels of the relative pigment biosynthetic genes, such as MpFasA2, MpFasB2, MpPKS5, mppR1, mppB, and mppE, were up-regulated at 35 °C. The two-stage temperature strategy is a potential method for producing water-soluble Monascus yellow pigments with strong yellow fluorescence.

摘要

红曲霉菌种能够产生具有聚酮结构的次生代谢产物。在本研究中,用红曲红CGMCC 10910进行液体发酵产生了四种胞外水溶性黄色素(Y1 - Y4),其中Y3和Y4具有强烈的黄色荧光。色素混合物的组成与发酵温度密切相关。当发酵温度从30℃升高到35℃时,主要色素从Y1转变为Y3和Y4。将温度升高到35℃改变了色素的代谢途径,抑制了Y1的生物合成并增强了Y3和Y4的生物合成。此外,在两阶段温度发酵条件下,Y1的产量无显著降低,而Y3和Y4的产量分别增加了98.21%和79.31%。相对色素生物合成基因,如MpFasA2、MpFasB2、MpPKS5、mppR1、mppB和mppE的表达水平在35℃时上调。两阶段温度策略是一种生产具有强烈黄色荧光的水溶性红曲黄色素的潜在方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/218f/5483225/1dc3222b2b83/13568_2017_441_Fig1_HTML.jpg

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