17 research outputs found

    Progress and Research Needs of Plant Biomass Degradation by Basidiomycete Fungi

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    Discovery and exploitation of the transcriptional regulatory system of pectinases in Aspergillus niger

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    Pectin is a plant cell wall polysaccharide made of mainly D-galacturonic acid (GA) subunits. The potency of the filamentous fungus Aspergillus niger to naturally secrete high amounts of pectinases to degrade pectin has been utilized for the industrial production of pectinases. Industrially produced pectinases by A. niger are subsequently used mainly in the food industry, and for the hydrolysis of plant biomass to produce renewable energy. In this thesis, the key players in the transcriptional regulatory system of pectinases in A. niger, such as the transcriptional activator GaaR, the repressor GaaX and the physiological inducer 2-keto-3-deoxy-L-galactonate, are discovered. Several approaches to exploit this system for increased or constitutive expression of the genes encoding pectinases are also presented, such as overexpression and constitutive activation of gaaR, accumulation of 2-keto-3-deoxy-L-galactonate, and deletion of gaaX or creA, the main transcriptional repressor involved in CCR.</p

    Functional analysis of three putative galactofuranosyltransferases with redundant functions in galactofuranosylation in Aspergillus niger

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    Galactofuranose (Galf)-containing glycostructures are important to secure the integrity of the fungal cell wall. Golgi-localized Galf-transferases (Gfs) have been identified in Aspergillus nidulans and Aspergillus fumigatus. BLASTp searches identified three putative Galf-transferases in Aspergillus niger. Phylogenetic analysis showed that they group in three distinct groups. Characterization of the three Galf-transferases in A. niger by constructing single, double, and triple mutants revealed that gfsA is most important for Galf biosynthesis. The growth phenotypes of the ΔgfsA mutant are less severe than that of the ΔgfsAC mutant, indicating that GfsA and GfsC have redundant functions. Deletion of gfsB did not result in any growth defect and combining ΔgfsB with other deletion mutants did not exacerbate the growth phenotype. RT-qPCR experiments showed that induction of the agsA gene was higher in the ΔgfsAC and ΔgfsABC compared to the single mutants, indicating a severe cell wall stress response after multiple gfs gene deletions.Microbial Biotechnolog
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