Li Cheng-Xi, Zhao Shuai, Luo Xue-Mei, Feng Jia-Xun
State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, Guangxi Research Center for Microbial and Enzyme Engineering Technology, College of Life Science and Technology, Guangxi University, Nanning, China.
Front Microbiol. 2020 Mar 27;11:520. doi: 10.3389/fmicb.2020.00520. eCollection 2020.
Genes involved in cellular processes undergo environment-dependent co-regulation, but the co-expression patterns of fungal cellulase and xylanase-encoding genes remain unclear. Here, we identified two novel carbon sources, methylcellulose and 2-hydroxyethyl cellulose, which efficiently induced the secretion of cellulases and xylanases in . Comparative transcriptomic analyses identified carbon source-specific transcriptional patterns, mainly including major cellulase and xylanase-encoding genes, genes involved in glycolysis/gluconeogenesis and the tricarboxylic acid cycle, and genes encoding transcription factors, transporters and G protein-coupled receptors. Moreover, the weighted correlation network analysis of time-course transcriptomes, generated 17 highly connected modules. Module MEivory, comprising 120 members, included major cellulase and xylanase-encoding genes, genes encoding the key regulators PoxClrB and PoxXlnR, and a cellodextrin transporter POX06051/CdtC, which were tightly correlated with the filter-paper cellulase, carboxymethylcellulase and xylanase activities in . An expression kinetic analysis indicated that members in MEivory were activated integrally by carbon sources, but their expressional levels were carbon source- and/or induction duration-dependent. Three uncharacterized regulatory genes in MEivory were identified, which regulate the production of cellulases and xylanases in . These findings provide insights into the mechanisms associated with the synthesis and secretion of fungal cellulases and xylanases, and a guide for application in biotechnology.
参与细胞过程的基因会经历环境依赖性的共调控,但真菌纤维素酶和木聚糖酶编码基因的共表达模式仍不清楚。在此,我们鉴定出两种新型碳源,甲基纤维素和2-羟乙基纤维素,它们能有效诱导[具体真菌名称未给出]分泌纤维素酶和木聚糖酶。比较转录组分析确定了碳源特异性转录模式,主要包括主要的纤维素酶和木聚糖酶编码基因、参与糖酵解/糖异生和三羧酸循环的基因,以及编码转录因子、转运蛋白和G蛋白偶联受体的基因。此外,对时间进程转录组进行的加权相关网络分析产生了17个高度连接的模块。包含120个成员的模块MEivory包括主要的纤维素酶和木聚糖酶编码基因、编码关键调节因子PoxClrB和PoxXlnR的基因,以及一个纤维糊精转运蛋白POX06051/CdtC,它们与[具体真菌名称未给出]中的滤纸纤维素酶、羧甲基纤维素酶和木聚糖酶活性紧密相关。表达动力学分析表明,MEivory中的成员被碳源整体激活,但其表达水平取决于碳源和/或诱导持续时间。在MEivory中鉴定出三个未表征的调控基因,它们调控[具体真菌名称未给出]中纤维素酶和木聚糖酶的产生。这些发现为真菌纤维素酶和木聚糖酶的合成与分泌相关机制提供了见解,并为其在生物技术中的应用提供了指导。