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ABSTRACT The ability of an inulosucrase (IS) from Lactobacillus gasseri DSM 20604 to synthesize fructooligosaccharides (FOS) and maltosylfructosides (MFOS) in the presence of sucrose and sucrose-maltose mixtures was investigated after optimization of synthesis conditions, including enzyme concentration, temperature, pH, and reaction time. The maximum formation of FOS, which consist of β-2,1-linked fructose to sucrose, was 45% (in weight with respect to the initial amount of sucrose) and was obtained after 24 h of reaction at 55°C in the presence of sucrose (300 g liter −1 ) and 1.6 U ml −1 of IS–25 mM sodium acetate buffer–1 mM CaCl 2 (pH 5.2). The production of MFOS was also studied as a function of the initial ratios of sucrose to maltose (10:50, 20:40, 30:30, and 40:20, expressed in g 100 ml −1 ). The highest yield in total MFOS was attained after 24 to 32 h of reaction time and ranged from 13% (10:50 sucrose/maltose) to 52% (30:30 sucrose/maltose) in weight with respect to the initial amount of maltose. Nuclear magnetic resonance (NMR) structural characterization indicated that IS from L. gasseri specifically transferred fructose moieties of sucrose to either C-1 of the reducing end or C-6 of the nonreducing end of maltose. Thus, the trisaccharide erlose [α- d -glucopyranosyl-(1→4)-α- d -glucopyranosyl-(1→2)-β- d -fructofuranoside] was the main synthesized MFOS followed by neo-erlose [β- d -fructofuranosyl-(2→6)-α- d -glucopyranosyl-(1→4)-α- d -glucopyranose]. The formation of MFOS with a higher degree of polymerization was also demonstrated by the transfer of additional fructose residues to C-1 of either the β-2,1-linked fructose or the β-2,6-linked fructose to maltose, revealing the capacity of MFOS to serve as acceptors.
Sucrose, Magnetic Resonance Spectroscopy, Time Factors, Temperature, Oligosaccharides, Hydrogen-Ion Concentration, Chromatography, Affinity, Gas Chromatography-Mass Spectrometry, Lactobacillus, Bioreactors, Hexosyltransferases, Bacterial Proteins, Rosaniline Dyes, Electrophoresis, Polyacrylamide Gel, Cloning, Molecular, Maltose, Trisaccharides, Chromatography, Liquid, DNA Primers
Sucrose, Magnetic Resonance Spectroscopy, Time Factors, Temperature, Oligosaccharides, Hydrogen-Ion Concentration, Chromatography, Affinity, Gas Chromatography-Mass Spectrometry, Lactobacillus, Bioreactors, Hexosyltransferases, Bacterial Proteins, Rosaniline Dyes, Electrophoresis, Polyacrylamide Gel, Cloning, Molecular, Maltose, Trisaccharides, Chromatography, Liquid, DNA Primers
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