Key Laboratory of Fermentation Engineering (Ministry of Education), National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), College of Bioengineering, Hubei University of Technology, Wuhan, Hubei430068, P.R. China.
ABI Group, College of Marine Science and Technology, Zhejiang Ocean University, Zhoushan, Zhejiang, Wuhan, Hubei 316022, China.
FEMS Yeast Res. 2022 Sep 3;22(1). doi: 10.1093/femsyr/foac040.
Zygosaccharomyces rouxii is an osmotolerant and halotolerant yeast that can participate in fermentation. To understand the mechanisms of salt and sugar tolerance, the transcription levels of Z. rouxii M 2013310 under 180 g/L NaCl stress and 600 g/L glucose stress were measured. The transcriptome analysis showed that 2227 differentially expressed genes (DEGs) were identified under 180 g/L NaCl stress, 1530 DEGs were identified under 600 g/L glucose stress, and 1278 DEGs were identified under both stress conditions. Then, KEGG enrichment analyses of these genes indicated that 53.3% of the upregulated genes were involved in the ergosterol synthesis pathway. Subsequently, quantitative PCR was used to verify the results, which showed that the genes of the ergosterol synthesis pathway were significantly upregulated under 180 g/L NaCl stress. Finally, further quantitative testing of ergosterol and spotting assays revealed that Z. rouxii M 2013310 increased the amount of ergosterol in response to high salt stress. These results highlighted the functional differences in ergosterol under sugar stress and salt stress, which contributes to our understanding of the tolerance mechanisms of salt and sugar in Z. rouxii.
鲁氏接合酵母是一种耐渗透压和耐盐的酵母,能够参与发酵。为了了解其耐盐和耐糖机制,我们测量了 Z. rouxii M 2013310 在 180 g/L NaCl 胁迫和 600 g/L 葡萄糖胁迫下的转录水平。转录组分析表明,在 180 g/L NaCl 胁迫下鉴定出 2227 个差异表达基因(DEGs),在 600 g/L 葡萄糖胁迫下鉴定出 1530 个 DEGs,在两种胁迫条件下共鉴定出 1278 个 DEGs。随后,对这些基因进行 KEGG 富集分析表明,上调基因中有 53.3%参与了麦角固醇合成途径。随后,我们使用定量 PCR 对结果进行了验证,结果表明,在 180 g/L NaCl 胁迫下,麦角固醇合成途径的基因显著上调。最后,进一步对麦角固醇进行定量检测和点样实验,结果表明 Z. rouxii M 2013310 能够响应高盐胁迫增加麦角固醇的含量。这些结果突出了麦角固醇在糖胁迫和盐胁迫下的功能差异,有助于我们理解 Z. rouxii 对盐和糖的耐受机制。