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OPTIMIZATION OF ENZYMATIC SYNTHESIS OF ISOMALTO-OLIGOSACCHARIDES PRODUCTION
Authors:M.C. RABELO,T.L. HONORATO,L.R.B. GONÇ  ALVES,G.A.S. PINTO, S. RODRIGUES
Affiliation:Departamento de Tecnologia de Alimentos
Universidade Federal do Ceará
Caixa Postal 12168, Bloco 858 Campus do Pici
60021-970 Fortaleza, CE, Brazil;
Departamento de Engenharia Química
Universidade Federal do Ceará
Bloco 709, Campus do Pici
60455-760 Fortaleza, CE, Brazil;
Embrapa Agroindústria Tropical
Laboratório de Bioprocessos
Rua Sara Mesquita, 2270 –Pici
Fortaleza, CE, Brazil
Abstract:Glucosyltransferases can be applied in the synthesis of prebiotic oligosaccharides. Enzymatic synthesis using acceptors can be used to obtain these carbohydrates. When maltose is the acceptor, oligosaccharides containing one maltose moiety and up to eight glucose units linked by α-1,6-glycosidic bonds are obtained as the product of dextransucrase acceptor reaction. In this work, the enzymatic synthesis of isomalto-oligosaccharides using dextransucrase from Leuconostoc mesenteroides NRRL B-512F was optimized by response surface methodology. The effect of maltose and sucrose concentrations on the acceptor reaction was evaluated in a batch reactor system. Partially purified enzyme was used to reduce the enzyme purification cost. The results showed that high sucrose concentrations in conjunction with high maltose levels enhanced the isomalto-oligosaccharide synthesis. A productivity of 42.95 mmol/L.h of isomalto-oligosaccharides was obtained at the optimal operating condition (100 mmol/L of sucrose and 200 mmol/L of maltose).

PRATICAL APPLICATIONS


Oligosaccharides as prebiotic have a large application in food formulations, and their beneficial role in human health have been extensively studied. Although the acceptor mechanism of dextransucrase has already been extensively studied, an industrial process has not been developed yet for enzyme synthesis of isomalto-oligosaccharide. The process studied in this work allows the large-scale preparation of isomalto-oligosaccharide using partially purified enzyme.
Keywords:
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