Preparation of α-galactooligoglycosides by cell walls from Cryptococcus laurentii using a novel α-galactosyl donor

• Published in: Tetrahedron: asymmetry 2017-08, Vol.28 (8), p.1089-1094
• Main Authors: Mastihuba, Vladimír, Mastihubová, Mária, Belák, Miroslav, Dudíková, Jana, Potocká, Elena Karnišová, Petruš, Ladislav
• Format: Article
• Language: English
• ISSN: 0957-4166; 1362-511X
• DOI: 10.1016/j.tetasy.2017.07.007

[Display omitted] The cell walls of an acapsular strain of the yeast Cryptococcus laurentii catalyze the regioselective formation of α-galactooligosaccharides through self-condensation of 4-nitrophenyl α-d-galactopyranoside and of a novel activated α-galactosyl donor 2,2,2-trifluoroethyl α-d-galactopyranoside. The latter substance can be easily prepared by several methods and is highly soluble in water and therefore can be used in higher initial concentrations suppressing secondary product hydrolysis. The preparative reaction catalyzed by cell walls provided 17.4% and 2% of corresponding 2,2,2-trifluoroethyl galactobioside and galactotrioside, respectively, while the reaction with 4-nitrophenyl α-d-galactopyranoside provided the corresponding 4-nitrophenyl galactobioside and galactotrioside in 6.6 and 2.5% yields, respectively. The reactions proceeded with strict α-(1→6)-regioselectivity.