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Acceptor Specificity of ß-N-Acetylhexosaminidase from Talaromyces flavus: A Rational Explanation.
Garcia-Oliva, Cecilia; Hoyos, Pilar; Petrásková, Lucie; Kulik, Natalia; Pelantová, Helena; Cabanillas, Alfredo H; Rumbero, Ángel; Kren, Vladimír; Hernáiz, María J; Bojarová, Pavla.
Afiliação
  • Garcia-Oliva C; Department of Chemistry in Pharmaceutical Sciences, Faculty of Pharmacy, Complutense University of Madrid, Plaza Ramón y Cajal, E 28040 Madrid, Spain.
  • Hoyos P; Department of Chemistry in Pharmaceutical Sciences, Faculty of Pharmacy, Complutense University of Madrid, Plaza Ramón y Cajal, E 28040 Madrid, Spain.
  • Petrásková L; Institute of Microbiology of the Czech Academy of Sciences, Vídenská 1083, CZ 14220 Prague 4, Czech Republic.
  • Kulik N; Institute of Microbiology of the Czech Academy of Sciences, Center for Nanobiology and Structural Biology, Zámek 136, CZ 37333 Nové Hrady, Czech Republic.
  • Pelantová H; Institute of Microbiology of the Czech Academy of Sciences, Vídenská 1083, CZ 14220 Prague 4, Czech Republic.
  • Cabanillas AH; Department of Organic Chemistry, Autonomous University of Madrid, Cantoblanco, 28049 Madrid, Spain.
  • Rumbero Á; Department of Organic Chemistry, Autonomous University of Madrid, Cantoblanco, 28049 Madrid, Spain.
  • Kren V; Institute of Microbiology of the Czech Academy of Sciences, Vídenská 1083, CZ 14220 Prague 4, Czech Republic.
  • Hernáiz MJ; Department of Chemistry in Pharmaceutical Sciences, Faculty of Pharmacy, Complutense University of Madrid, Plaza Ramón y Cajal, E 28040 Madrid, Spain.
  • Bojarová P; Institute of Microbiology of the Czech Academy of Sciences, Vídenská 1083, CZ 14220 Prague 4, Czech Republic.
Int J Mol Sci ; 20(24)2019 Dec 07.
Article em En | MEDLINE | ID: mdl-31817903
Fungal ß-N-acetylhexosaminidases, though hydrolytic enzymes in vivo, are useful tools in the preparation of oligosaccharides of biological interest. The ß-N-acetylhexosaminidase from Talaromyces flavus is remarkable in terms of its synthetic potential, broad substrate specificity, and tolerance to substrate modifications. It can be heterologously produced in Pichia pastoris in a high yield. The mutation of the Tyr470 residue to histidine greatly enhances its transglycosylation capability. The aim of this work was to identify the structural requirements of this model ß-N-acetylhexosaminidase for its transglycosylation acceptors and formulate a structure-activity relationship study. Enzymatic reactions were performed using an activated glycosyl donor, 4-nitrophenyl N-acetyl-ß-d-glucosaminide or 4-nitrophenyl N-acetyl-ß-d-galactosaminide, and a panel of glycosyl acceptors of varying structural features (N-acetylglucosamine, glucose, N-acetylgalactosamine, galactose, N-acetylmuramic acid, and glucuronic acid). The transglycosylation products were isolated and structurally characterized. The C-2 N-acetamido group in the acceptor molecule was found to be essential for recognition by the enzyme. The presence of the C-2 hydroxyl moiety strongly hindered the normal course of transglycosylation, yielding unique non-reducing disaccharides in a low yield. Moreover, whereas the gluco-configuration at C-4 steered the glycosylation into the ß(1-4) position, the galacto-acceptor afforded a ß(1-6) glycosidic linkage. The Y470H mutant enzyme was tested with acceptors based on ß-glycosides of uronic acid and N-acetylmuramic acid. With the latter acceptor, we were able to isolate and characterize one glycosylation product in a low yield. To our knowledge, this is the first example of enzymatic glycosylation of an N-acetylmuramic acid derivative. In order to explain these findings and predict enzyme behavior, a modeling study was accomplished that correlated with the acquired experimental data.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oligossacarídeos / Beta-N-Acetil-Hexosaminidases / Talaromyces / Glicosídeos Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oligossacarídeos / Beta-N-Acetil-Hexosaminidases / Talaromyces / Glicosídeos Idioma: En Ano de publicação: 2019 Tipo de documento: Article