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A Mitogen-Activated Protein Kinase Tmk3 Participates in High Osmolarity Resistance Cell Wall Integrity Maintenance and Cellulase Production Regulation in Trichoderma reesei

机译:丝裂原激活的蛋白激酶Tmk3参与里氏木霉的高渗透压抵抗细胞壁完整性维持和纤维素酶生产调节。

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摘要

The mitogen-activated protein kinase (MAPK) pathways are important signal transduction pathways conserved in essentially all eukaryotes, but haven't been subjected to functional studies in the most important cellulase-producing filamentous fungus Trichoderma reesei. Previous reports suggested the presence of three MAPKs in T. reesei: Tmk1, Tmk2, and Tmk3. By exploring the phenotypic features of T. reesei Δtmk3, we first showed elevated NaCl sensitivity and repressed transcription of genes involved in glycerol/trehalose biosynthesis under higher osmolarity, suggesting Tmk3 participates in high osmolarity resistance via derepression of genes involved in osmotic stabilizer biosynthesis. We also showed significant downregulation of genes encoding chitin synthases and a β-1,3-glucan synthase, decreased chitin content, ‘budded’ hyphal appearance typical to cell wall defective strains, and increased sensitivity to calcofluor white/Congo red in the tmk3 deficient strain, suggesting Tmk3 is involved in cell wall integrity maintenance in T. reesei. We further observed the decrease of cellulase transcription and production in T. reesei Δtmk3 during submerged cultivation, as well as the presence of MAPK phosphorylation sites on known transcription factors involved in cellulase regulation, suggesting Tmk3 is also involved in the regulation of cellulase production. Finally, the expression of cell wall integrity related genes, the expression of cellulase coding genes, cellulase production and biomass accumulation were compared between T. reesei Δtmk3 grown in solid state media and submerged media, showing a strong restoration effect in solid state media from defects resulted from tmk3 deletion. These results showed novel physiological processes that fungal Hog1-type MAPKs are involved in, and present the first experimental investigation of MAPK signaling pathways in T. reesei. Our observations on the restoration effect during solid state cultivation suggest that T. reesei is evolved to favor solid state growth, bringing up the proposal that the submerged condition normally used during investigations on fungal physiology might be misleading.
机译:丝裂原激活的蛋白激酶(MAPK)通路是基本上在所有真核生物中都保守的重要信号转导通路,但尚未在产生纤维素酶的最重要的丝状真菌里氏木霉中进行功能研究。以前的报告表明里氏木霉中存在三种MAPK:Tmk1,Tmk2和Tmk3。通过探索里氏木霉Δtmk3的表型特征,我们首先显示了NaCl敏感性升高和高渗透压下参与甘油/海藻糖生物合成的基因的转录受到抑制,这表明Tmk3通过抑制参与渗透压稳定剂生物合成的基因而参与了高渗透压抗性。我们还显示出编码几丁质合酶和β-1,3-葡聚糖合酶的基因显着下调,几丁质含量降低,细胞壁缺陷菌株常见的“预算化”菌丝外观,以及在tmk3缺陷型中对钙荧光白/刚果红的敏感性增加。菌株,表明Tmk3参与里氏木霉的细胞壁完整性维持。我们进一步观察到,在水下培养过程中,里氏木霉Δtmk3的纤维素酶转录和产量减少,以及参与纤维素酶调节的已知转录因子上MAPK磷酸化位点的存在,表明Tmk3也参与了纤维素酶生产的调节。最后,比较了在固态培养基和淹没培养基中生长的里氏木霉Δtmk3的细胞壁完整性相关基因的表达,纤维素酶编码基因的表达,纤维素酶的产生和生物量的积累,显示了在固态培养基中从缺陷中恢复的强大作用。是由于tmk3删除引起的。这些结果表明真菌Hog1型MAPK参与了新的生理过程,并提出了里氏木霉MAPK信号通路的首次实验研究。我们对固态培养过程中恢复作用的观察表明,里氏木霉进化为有利于固态生长,提出了关于真菌生理学研究中通常使用的淹没条件可能产生误导的提议。

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