Expression-based clustering of CAZyme-encoding genes of Aspergillus niger

被引:44
作者
Gruben, Birgit S. [1 ,2 ]
Makela, Miia R. [1 ,3 ,4 ]
Kowalczyk, Joanna E. [1 ,3 ]
Zhou, Miaomiao [1 ,5 ]
Benoit-Gelber, Isabelle [1 ,2 ,3 ,6 ]
De Vries, Ronald P. [1 ,2 ]
机构
[1] Westerdijk Fungal Biodivers Inst, Fungal Physiol, Uppsalalaan 8, NL-3584 CT Utrecht, Netherlands
[2] Univ Utrecht, Microbiol, Padualaan 8, NL-3584 CH Utrecht, Netherlands
[3] Univ Utrecht, Fungal Mol Physiol, Uppsalalaan 8, NL-3584 CT Utrecht, Netherlands
[4] Univ Helsinki, Viikki Bioctr 1, Div Microbiol & Biotechnol, Dept Food & Environm Sci, Helsinki, Finland
[5] Avans Univ Appl Sci, ATGM, Lovensdijkstr 61-63, NL-4818 AJ Breda, Netherlands
[6] Concordia Univ, Ctr Struct & Funct Genom, 7141 Sherbrooke St W, Montreal, PQ, Canada
来源
BMC GENOMICS | 2017年 / 18卷
关键词
Transcriptional regulators; Plant biomass degradation; CAZy genes; XlnR; AmyR; GalX; AraR; RhaR; Aspergillus niger; TRANSCRIPTIONAL ACTIVATOR XLNR; MANNAN UTILIZATION SYSTEM; D-GALACTURONIC ACID; ALPHA-GALACTOSIDASE; MOLECULAR-CLONING; AMYLASE GENES; DEGRADATION; ENZYMES; PATHWAY; PECTIN;
D O I
10.1186/s12864-017-4164-x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: The Aspergillus niger genome contains a large repertoire of genes encoding carbohydrate active enzymes (CAZymes) that are targeted to plant polysaccharide degradation enabling A. niger to grow on a wide range of plant biomass substrates. Which genes need to be activated in certain environmental conditions depends on the composition of the available substrate. Previous studies have demonstrated the involvement of a number of transcriptional regulators in plant biomass degradation and have identified sets of target genes for each regulator. In this study, a broad transcriptional analysis was performed of the A. niger genes encoding (putative) plant polysaccharide degrading enzymes. Microarray data focusing on the initial response of A. niger to the presence of plant biomass related carbon sources were analyzed of a wild-type strain N402 that was grown on a large range of carbon sources and of the regulatory mutant strains Delta xlnR, Delta araR, Delta amyR, Delta rhaR and Delta galX that were grown on their specific inducing compounds. Results: The cluster analysis of the expression data revealed several groups of co-regulated genes, which goes beyond the traditionally described co-regulated gene sets. Additional putative target genes of the selected regulators were identified, based on their expression profile. Notably, in several cases the expression profile puts questions on the function assignment of uncharacterized genes that was based on homology searches, highlighting the need for more extensive biochemical studies into the substrate specificity of enzymes encoded by these non-characterized genes. The data also revealed sets of genes that were upregulated in the regulatory mutants, suggesting interaction between the regulatory systems and a therefore even more complex overall regulatory network than has been reported so far. Conclusions: Expression profiling on a large number of substrates provides better insight in the complex regulatory systems that drive the conversion of plant biomass by fungi. In addition, the data provides additional evidence in favor of and against the similarity-based functions assigned to uncharacterized genes.
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页数:18
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