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Tytuł pozycji:

Transcriptome analysis of Aspergillus niger xlnR and xkiA mutants grown on corn Stover and soybean hulls reveals a highly complex regulatory network.

Tytuł:
Transcriptome analysis of Aspergillus niger xlnR and xkiA mutants grown on corn Stover and soybean hulls reveals a highly complex regulatory network.
Autorzy:
Khosravi C; Fungal Physiology, Westerdijk Fungal Biodiversity Institute & Fungal Molecular Physiology, Utrecht University, Utrecht, the Netherlands.
Kowalczyk JE; Fungal Physiology, Westerdijk Fungal Biodiversity Institute & Fungal Molecular Physiology, Utrecht University, Utrecht, the Netherlands.
Chroumpi T; Fungal Physiology, Westerdijk Fungal Biodiversity Institute & Fungal Molecular Physiology, Utrecht University, Utrecht, the Netherlands.
Battaglia E; Fungal Physiology, Westerdijk Fungal Biodiversity Institute & Fungal Molecular Physiology, Utrecht University, Utrecht, the Netherlands.
Aguilar Pontes MV; Fungal Physiology, Westerdijk Fungal Biodiversity Institute & Fungal Molecular Physiology, Utrecht University, Utrecht, the Netherlands.
Peng M; Fungal Physiology, Westerdijk Fungal Biodiversity Institute & Fungal Molecular Physiology, Utrecht University, Utrecht, the Netherlands.
Wiebenga A; Fungal Physiology, Westerdijk Fungal Biodiversity Institute & Fungal Molecular Physiology, Utrecht University, Utrecht, the Netherlands.
Ng V; US Department of Energy Joint Genome Institute, Walnut Creek, CA, USA.
Lipzen A; US Department of Energy Joint Genome Institute, Walnut Creek, CA, USA.
He G; US Department of Energy Joint Genome Institute, Walnut Creek, CA, USA.
Bauer D; US Department of Energy Joint Genome Institute, Walnut Creek, CA, USA.
Grigoriev IV; US Department of Energy Joint Genome Institute, Walnut Creek, CA, USA.; Department of Plant and Microbial Biology, University of California, Berkeley, CA, USA.
de Vries RP; Fungal Physiology, Westerdijk Fungal Biodiversity Institute & Fungal Molecular Physiology, Utrecht University, Utrecht, the Netherlands. .
Źródło:
BMC genomics [BMC Genomics] 2019 Nov 14; Vol. 20 (1), pp. 853. Date of Electronic Publication: 2019 Nov 14.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Original Publication: London : BioMed Central, [2000-
MeSH Terms:
Gene Expression Profiling*
Mutation*
Transcriptome*
Aspergillus niger/*genetics
Glycine max/*microbiology
Zea mays/*microbiology
Aspergillus niger/growth & development ; Biodegradation, Environmental ; Biomass ; Cellulose/chemistry ; Cellulose/metabolism ; Fungal Proteins/genetics ; Fungal Proteins/metabolism ; Gene Deletion ; Gene Expression Regulation, Fungal ; Hydrolysis
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Grant Information:
016.130.609 Dutch Technology Foundation STW, Applied Science division of NWO; ALWOP.233 Dutch Scientific Organization (NWO); DE-AC02-05CH11231 Office of Science of the U.S. Department of Energy
Contributed Indexing:
Keywords: Aspergillus Niger; Gene expression; Transcriptomics; XkiA; XlnR
Substance Nomenclature:
0 (Fungal Proteins)
9004-34-6 (Cellulose)
Entry Date(s):
Date Created: 20191116 Date Completed: 20200330 Latest Revision: 20231213
Update Code:
20240105
PubMed Central ID:
PMC6854810
DOI:
10.1186/s12864-019-6235-7
PMID:
31726994
Czasopismo naukowe
Background: Enzymatic plant biomass degradation by fungi is a highly complex process and one of the leading challenges in developing a biobased economy. Some industrial fungi (e.g. Aspergillus niger) have a long history of use with respect to plant biomass degradation and for that reason have become 'model' species for this topic. A. niger is a major industrial enzyme producer that has a broad ability to degrade plant based polysaccharides. A. niger wild-type, the (hemi-)cellulolytic regulator (xlnR) and xylulokinase (xkiA1) mutant strains were grown on a monocot (corn stover, CS) and dicot (soybean hulls, SBH) substrate. The xkiA1 mutant is unable to utilize the pentoses D-xylose and L-arabinose and the polysaccharide xylan, and was previously shown to accumulate inducers for the (hemi-)cellulolytic transcriptional activator XlnR and the arabinanolytic transcriptional activator AraR in the presence of pentoses, resulting in overexpression of their target genes. The xlnR mutant has reduced growth on xylan and down-regulation of its target genes. The mutants therefore have a similar phenotype on xylan, but an opposite transcriptional effect. D-xylose and L-arabinose are the most abundant monosaccharides after D-glucose in nearly all plant-derived biomass materials. In this study we evaluated the effect of the xlnR and xkiA1 mutation during growth on two pentose-rich substrates by transcriptome analysis.
Results: Particular attention was given to CAZymes, metabolic pathways and transcription factors related to the plant biomass degradation. Genes coding for the main enzymes involved in plant biomass degradation were down-regulated at the beginning of the growth on CS and SBH. However, at a later time point, significant differences were found in the expression profiles of both mutants on CS compared to SBH.
Conclusion: This study demonstrates the high complexity of the plant biomass degradation process by fungi, by showing that mutant strains with fairly straightforward phenotypes on pure mono- and polysaccharides, have much less clear-cut phenotypes and transcriptomes on crude plant biomass.
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