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Galactose metabolism and toxicity in Ustilago maydis.
Schuler, David; Höll, Christina; Grün, Nathalie; Ulrich, Jonas; Dillner, Bastian; Klebl, Franz; Ammon, Alexandra; Voll, Lars M; Kämper, Jörg.
Afiliación
  • Schuler D; Karlsruhe Institute of Technology, Institute for Applied Biosciences, Department of Genetics, Fritz Haber Weg 4, 76131 Karlsruhe, Germany.
  • Höll C; Karlsruhe Institute of Technology, Institute for Applied Biosciences, Department of Genetics, Fritz Haber Weg 4, 76131 Karlsruhe, Germany.
  • Grün N; Karlsruhe Institute of Technology, Institute for Applied Biosciences, Department of Genetics, Fritz Haber Weg 4, 76131 Karlsruhe, Germany.
  • Ulrich J; Karlsruhe Institute of Technology, Institute for Applied Biosciences, Department of Genetics, Fritz Haber Weg 4, 76131 Karlsruhe, Germany.
  • Dillner B; Karlsruhe Institute of Technology, Institute for Applied Biosciences, Department of Genetics, Fritz Haber Weg 4, 76131 Karlsruhe, Germany.
  • Klebl F; FAU Erlangen-Nuremberg, Department of Biology, Molecular Plant Physiology, Staudtstrasse 5, 91058 Erlangen, Germany.
  • Ammon A; Philips-University of Marburg, Department of Biology, Plant Physiology and Photo Biology, Karl von Frisch Strasse 8, 35043 Marburg, Germany.
  • Voll LM; Philips-University of Marburg, Department of Biology, Plant Physiology and Photo Biology, Karl von Frisch Strasse 8, 35043 Marburg, Germany.
  • Kämper J; Karlsruhe Institute of Technology, Institute for Applied Biosciences, Department of Genetics, Fritz Haber Weg 4, 76131 Karlsruhe, Germany. Electronic address: joerg.kaemper@kit.edu.
Fungal Genet Biol ; 114: 42-52, 2018 05.
Article en En | MEDLINE | ID: mdl-29580862
In most organisms, galactose is metabolized via the Leloir pathway, which is conserved from bacteria to mammals. Utilization of galactose requires a close interplay of the metabolic enzymes, as misregulation or malfunction of individual components can lead to the accumulation of toxic intermediate compounds. For the phytopathogenic basidiomycete Ustilago maydis, galactose is toxic for wildtype strains, i.e. leads to growth repression despite the presence of favorable carbon sources as sucrose. The galactose sensitivity can be relieved by two independent modifications: (1) by disruption of Hxt1, which we identify as the major transporter for galactose, and (2) by a point mutation in the gene encoding the galactokinase Gal1, the first enzyme of the Leloir pathway. The mutation in gal1(Y67F) leads to reduced enzymatic activity of Gal1 and thus may limit the formation of putatively toxic galactose-1-phosphate. However, systematic deletions and double deletions of different genes involved in galactose metabolism point to a minor role of galactose-1-phosphate in galactose toxicity. Our results show that molecular triggers for galactose toxicity in U. maydis differ from yeast and mammals.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ustilago / Galactosa Idioma: En Revista: Fungal Genet Biol Asunto de la revista: GENETICA / MICROBIOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ustilago / Galactosa Idioma: En Revista: Fungal Genet Biol Asunto de la revista: GENETICA / MICROBIOLOGIA Año: 2018 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos