Bioscience, Biotechnology, and Biochemistry
Online ISSN : 1347-6947
Print ISSN : 0916-8451
Enzymatic Synthesis of Mannosyl-cyclodextrin by α-Mannosidase from Jack Bean
Kenichi HAMAYASUKoji HARAKoki FUJITAYukio KONDOHitoshi HASHIMOTOToshiko TANIMOTOKyoko KOIZUMIHirofumi NAKANOSumio KITAHATA
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1997 Volume 61 Issue 5 Pages 825-829

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Abstract

Mannosylated derivatives of cyclodextrins (CDs), mannosyl-α, β, and γCD were synthesized from a mixture of mannose and α, β, and γCD by the reverse action of α-mannosidase from jack bean, respectively. Their structures were analyzed by FAB-MS and 13C-NMR spectroscopies, and they were identified as 6-O-α-D-mannosyl-α, β, and γCD. The optimum conditions for the production of 6-O-α-D-mannosyl-αCD by α-mannosidase were examined. Optimum pH and temperature were pH 4.5 and 60°C, respectively. Yield of mannosyl-αCD increased with increasing mannose concentration and reached more than 35% (mol/mol) at the concentration of 2 M mannose and 0.4 M αCD.

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© Japan Society for Bioscience, Biotechnology, and Agrochemistry
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