Lipase-Catalyzed Solid-Phase Synthesis of Sugar Esters, IV: Selectivity of Lipases Towards Primary and Secondary Hydroxyl Groups in Carbohydrates

التفاصيل البيبلوغرافية
العنوان: Lipase-Catalyzed Solid-Phase Synthesis of Sugar Esters, IV: Selectivity of Lipases Towards Primary and Secondary Hydroxyl Groups in Carbohydrates
المؤلفون: Uwe T. Bornscheuer, Rolf D. Schmid, Linqiu Cao
المصدر: Biocatalysis and Biotransformation. 16:249-257
بيانات النشر: Informa UK Limited, 1998.
سنة النشر: 1998
مصطلحات موضوعية: chemistry.chemical_classification, biology, Triacylglycerol lipase, Fatty acid, Fructose, biology.organism_classification, Biochemistry, Catalysis, Palmitic acid, Acylation, chemistry.chemical_compound, chemistry, biology.protein, Organic chemistry, lipids (amino acids, peptides, and proteins), Candida antarctica, Lipase, Selectivity, Biotechnology
الوصف: The acylation of several pyranoses and fructose with fatty acids by lipases in a solid-phase system was investigated. Highest selectivity was found using lipase from Candida antarctica B immobilized on polypropylene EP 100. For β-D(+)-glucose 98% mono- and 2% diacylation using palmitic acid in t-butanol were observed. Much lower selectivities were achieved with D-(+)-mannose (75% monoacylation) and D(+)-galactose (50% monoacylation), which was explained by the different orientation of the C2-hydroxyl groups. The selectivity in the acylation of fructose was significantly influenced by the fatty acid chain length and the organic solvent. Monoacylation was favored in less hydrophobic solvents (e.g. t-butanol) using long chain fatty acids.
تدمد: 1029-2446
1024-2422
DOI: 10.3109/10242429809003620
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::0677dea571a51fee6be927aae2cc0261
https://doi.org/10.3109/10242429809003620
رقم الانضمام: edsair.doi...........0677dea571a51fee6be927aae2cc0261
قاعدة البيانات: OpenAIRE
الوصف
تدمد:10292446
10242422
DOI:10.3109/10242429809003620