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Enzymatic synthesis of N-acetylglucosaminobioses by reverse hydrolysis: characterisation and application of the library of fungal betta-N-acetylhexosaminidases
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SYSNO ASEP 0100392 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Ostatní články Title Enzymatic synthesis of N-acetylglucosaminobioses by reverse hydrolysis: characterisation and application of the library of fungal betta-N-acetylhexosaminidases Title Enzymatické syntézy N-acetylglucosaminobióz pomocí reverzní hydrolýzy: characterizace a aplikace knihovny houbových beta-N-acetylhexosaminidáz Author(s) Rauvolfová, Jana (MBU-M)
Weignerová, Lenka (MBU-M) RID
Kuzma, Marek (MBU-M) ORCID, RID
Přikrylová, Věra (MBU-M)
Macková, M. (CZ)
Pišvejcová, Andrea (UOCHB-X)
Křen, Vladimír (MBU-M) RID, ORCIDSource Title Journal of Molecular Catalysis B-Enzymatic. - : Elsevier - ISSN 1381-1177
Roč. 29, - (2004), s. 259-264Number of pages 6 s. Language eng - English Country NL - Netherlands Keywords reverse hydrolysis ; enzymatic synthesis ; filamentous fungi Subject RIV EE - Microbiology, Virology R&D Projects GP204/02/P096 GA ČR - Czech Science Foundation (CSF) CEZ AV0Z5020903 - MBU-M Annotation Two novel deoxysugar esters, named enteridinines A and B, were isolated from the slime mold Enteridium lycoperdon. Their structures, including the absolute configurations of the hydroxyl and methyl groups, were determined by means of extensive spectroscopic data such as UV, IR, MS, 1D and 2D NMR spectra. Enteridinines A and B have unique structures containing 1,7-dioxaspiro[5.5]undecanes with an O-β-D-mycarosyl-(1→4)-β-D-olivosyl and an O-β-L-olivomycosyl-(1→4)-β-D-amicetosyl-(1→4)-β-D-digitoxosyl unit, respectively, and showed growth inhibitory activities against Gram positive bacteria. Workplace Institute of Microbiology Contact Eliška Spurná, eliska.spurna@biomed.cas.cz, Tel.: 241 062 231 Year of Publishing 2005
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