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Transcription factor Xpp1 is a switch between primary and secondary fungal metabolism.
Derntl, Christian; Kluger, Bernhard; Bueschl, Christoph; Schuhmacher, Rainer; Mach, Robert L; Mach-Aigner, Astrid R.
Afiliación
  • Derntl C; Research Area Biochemical Technology, Institute of Chemical Engineering, TU Wien, A-1060 Vienna, Austria.
  • Kluger B; Center for Analytical Chemistry, Department of Agrobiotechnology, University of Natural Resources and Life Sciences, A-3430 Tulln, Austria.
  • Bueschl C; Center for Analytical Chemistry, Department of Agrobiotechnology, University of Natural Resources and Life Sciences, A-3430 Tulln, Austria.
  • Schuhmacher R; Center for Analytical Chemistry, Department of Agrobiotechnology, University of Natural Resources and Life Sciences, A-3430 Tulln, Austria.
  • Mach RL; Research Area Biochemical Technology, Institute of Chemical Engineering, TU Wien, A-1060 Vienna, Austria.
  • Mach-Aigner AR; Research Area Biochemical Technology, Institute of Chemical Engineering, TU Wien, A-1060 Vienna, Austria; astrid.mach-aigner@tuwien.ac.at.
Proc Natl Acad Sci U S A ; 114(4): E560-E569, 2017 01 24.
Article en En | MEDLINE | ID: mdl-28074041
ABSTRACT
Fungi can produce a wide range of chemical compounds via secondary metabolism. These compounds are of major interest because of their (potential) application in medicine and biotechnology and as a potential source for new therapeutic agents and drug leads. However, under laboratory conditions, most secondary metabolism genes remain silent. This circumstance is an obstacle for the production of known metabolites and the discovery of new secondary metabolites. In this study, we describe the dual role of the transcription factor Xylanase promoter binding protein 1 (Xpp1) in the regulation of both primary and secondary metabolism of Trichoderma reesei Xpp1 was previously described as a repressor of xylanases. Here, we provide data from an RNA-sequencing analysis suggesting that Xpp1 is an activator of primary metabolism. This finding is supported by our results from a Biolog assay determining the carbon source assimilation behavior of an xpp1 deletion strain. Furthermore, the role of Xpp1 as a repressor of secondary metabolism is shown by gene expression analyses of polyketide synthases and the determination of the secondary metabolites of xpp1 deletion and overexpression strains using an untargeted metabolomics approach. The deletion of Xpp1 resulted in the enhanced secretion of secondary metabolites in terms of diversity and quantity. Homologs of Xpp1 are found among a broad range of fungi, including the biocontrol agent Trichoderma atroviride, the plant pathogens Fusarium graminearum and Colletotrichum graminicola, the model organism Neurospora crassa, the human pathogen Sporothrix schenckii, and the ergot fungus Claviceps purpurea.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Factores de Transcripción / Trichoderma / Proteínas Fúngicas / Metabolismo Secundario Tipo de estudio: Prognostic_studies Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2017 Tipo del documento: Article País de afiliación: Austria

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Factores de Transcripción / Trichoderma / Proteínas Fúngicas / Metabolismo Secundario Tipo de estudio: Prognostic_studies Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2017 Tipo del documento: Article País de afiliación: Austria