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qNMR for profiling the production of fungal secondary metabolites.
Brooks, Wilson C; Paguigan, Noemi D; Raja, Huzefa A; Moy, Franklin J; Cech, Nadja B; Pearce, Cedric J; Oberlies, Nicholas H.
Afiliação
  • Brooks WC; Department of Chemistry and Biochemistry, University of North Carolina at Greensboro, PO Box 26170, Greensboro, NC, 27402, USA.
  • Paguigan ND; Department of Chemistry and Biochemistry, University of North Carolina at Greensboro, PO Box 26170, Greensboro, NC, 27402, USA.
  • Raja HA; Department of Chemistry and Biochemistry, University of North Carolina at Greensboro, PO Box 26170, Greensboro, NC, 27402, USA.
  • Moy FJ; Department of Chemistry and Biochemistry, University of North Carolina at Greensboro, PO Box 26170, Greensboro, NC, 27402, USA.
  • Cech NB; Department of Chemistry and Biochemistry, University of North Carolina at Greensboro, PO Box 26170, Greensboro, NC, 27402, USA.
  • Pearce CJ; Mycosynthetix, Inc, 505 Meadowland Drive, Suite 103, Hillsborough, NC, 27278, USA.
  • Oberlies NH; Department of Chemistry and Biochemistry, University of North Carolina at Greensboro, PO Box 26170, Greensboro, NC, 27402, USA.
Magn Reson Chem ; 55(7): 670-676, 2017 Jul.
Article em En | MEDLINE | ID: mdl-28024162
ABSTRACT
Analysis of complex mixtures is a common challenge in natural products research. Quantitative nuclear magnetic resonance spectroscopy offers analysis of complex mixtures at early stages and with benefits that are orthogonal to more common methods of quantitation, including ultraviolet absorption spectroscopy and mass spectrometry. Several experiments were conducted to construct a methodology for use in analysis of extracts of fungal cultures. A broadly applicable method was sought for analysis of both pure and complex samples through use of an externally calibrated method. This method has the benefit of not contaminating valuable samples with the calibrant, and it passed scrutiny for line fitting and reproducibility. The method was implemented to measure the yield of griseofulvin and dechlorogriseofulvin from three fungal isolates. An isolate of Xylaria cubensis (coded MSX48662) was found to biosynthesize griseofulvin in the greatest yield, 149 ± 8 mg per fermentation, and was selected for further supply experiments. Copyright © 2016 John Wiley & Sons, Ltd.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Produtos Biológicos / Espectroscopia de Ressonância Magnética / Fungos Idioma: En Revista: Magn Reson Chem Assunto da revista: QUIMICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Produtos Biológicos / Espectroscopia de Ressonância Magnética / Fungos Idioma: En Revista: Magn Reson Chem Assunto da revista: QUIMICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos