A new enzyme catalysis: 3,4-dioxidation of some aryl β-D- glycopyranosides by fungal pyranose dehydrogenase

Tetrahedron Letters

Volumn 45, Issue 47, 2004, Pages 8677-8680

  Sedmera, Petr ^a   Halada, Petr ^a   Peterbauer, Clemens ^b   Volc, Jindřich ^a  

^a INSTITUTE OF MICROBIOLOGY   (Czech Republic)

^b UNIVERSITY OF NATURAL RESOURCES AND LIFE SCIENCES   (Austria)

Author keywords

3,4 Didehydroglucopyranoside; 3,4 Didehydroxylopyranoside; Agaricus; Aldopyranosid 3,4 diuloses; Aryl glycoside oxidation; Pyranose dehydrogenase; Sugar 3,4 dioxidation

Indexed keywords

BETA DEXTRO GLYCOPYRANOSIDE; CARBOHYDRATE; CARBONYL DERIVATIVE; FUNGAL ENZYME; GLUCOPYRANOSIDE; GLYCOPYRANOSIDE; GLYCOSIDE; OXIDOREDUCTASE; PYRANOSE DEHYDROGENASE; PYRANOSIDE; UNCLASSIFIED DRUG; XYLOPYRANOSIDE;

AGARICUS; AGARICUS MELEAGRIS; AQUEOUS SOLUTION; ARTICLE; BASIDIOMYCETES; CATALYSIS; CHEMICAL REACTION; ENZYME ACTIVITY; ENZYME PURIFICATION; HYDRATION; NUCLEAR MAGNETIC RESONANCE; OXIDATION; STRUCTURE ANALYSIS;

AGARICUS; MELEAGRIS;

EID: 7044235562     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.09.149     Document Type: Article

References (17)

1. E. Stoppok, J. Walter, and K. Buchholz Appl. Microbiol. Biotechnol. 43 1995 706 712
2. M. Pietsch, M. Walter, and K. Buchholz Carbohydr. Res. 254 1994 183 194
3. J. Volc, P. Sedmera, M. Kujawa, P. Halada, E. Kubátová, and D. Haltrich J. Mol. Catal. B: Enzym. 30 2004 177 184
4. J. Volc, P. Sedmera, P. Halada, V. Přikrylová, and G. Daniel Carbohydr. Res. 310 1998 151 156
5. J. Volc, P. Sedmera, P. Halada, G. Daniel, V. Přikrylová, and D. Haltrich J. Mol. Catal. B: Enzym. 17 2002 91 100
6. J. Volc, E. Kubátová, G. Daniel, P. Sedmera, and D. Haltrich Arch. Microbiol. 176 2001 178 186
7. J. Volc, P. Sedmera, P. Halada, V. Přikrylová, and D. Haltrich Carbohydr. Res. 329 2000 219 225
8. 13C NMR and HMBC) was undertaken to determine the structure and proportions of the products
9. The spectra were recorded on a LCQ Deca ion trap mass spectrometer equipped with a nanospray ion source. Samples, dissolved in 30% aqueous acetonitrile, were sprayed directly from EconoTip™ emitters. Spray voltage was 1.2 kV and the heated capillary was kept at 150°C. Only the final reaction mixtures were studied
10. S. Freimund, A. Huwig, F. Giffhorn, and S. Köpper Chem. Eur. J. 4 1998 2442 2455
11. F. Kiuchi, H.M. Liu, and Y. Tsuda Chem. Pharm. Bull. 38 1990 2326 2328
12. B.P. Gering Jr., and M. Wichtl Phytochemistry 26 1987 3011 3013
13. J. Volc, P. Sedmera, V. Havlíček, V. Př ikrylová, and G. Daniel Carbohydr. Res. 278 1995 59 70
14. P. Sedmera, J. Volc, V. Havlíček, S. Pakhomova, and A. Jegorov Carbohydr. Res. 297 1997 375 378
15. J. Volc, P. Sedmera, P. Halada, P. Dwivedi, and M. Costa-Fereira J. Carbohydr. Chem. 22 2003 207 216
16. H. Franzyk, C.E. Olsen, and S.R. Jensen J. Nat. Prod. 67 2004 1052 1054
17. S.J. Angyal, D.C. Craig, and A. Kuszman J. Carbohydr. Res. 194 1989 21 29