An unusual GH1 β-glucosidase from marine sediment with β-galactosidase and transglycosidation activities for superior galacto-oligosaccharide synthesis.

Abstract

A novel β-glucosidase, BglD1 with high β-galactosidase and transglycosidation activities, was screened and cloned from the deep-sea bacterium Bacillus sp. D1. BglD1 exhibited the maximal β-glucosidase and β-galactosidase activities at 55-60°C and pH5.5-6.0. The enzyme maintained approximately 50% of its original activity at 35°C and pH6.0 after 120-h incubation. When applied to synthesize galacto-oligosaccharides (GOS), BglD1 generated 118.3g/L GOS (33.8% (w/w)) from 350g/L lactose, with trisaccharide Gal-β(1 → 3)-Lac and disaccharide Gal-β(1 → 4)-Gal as the main components. Furthermore, BglD1 could hydrolyze lactose in milk and produce GOS simultaneously. Using milk as the substrate, BglD1 hydrolyzed 88.5% lactose and produced 3.3g/L GOS after incubation at 30°C for 1h. To improve the transglycosidation activity, a mutant BglD1:E224T was generated based on the semi-rational design. The GOS yield of BglD1:E224T was 11.5% higher than that of BglD1 when using lactose solution as the substrate. Thus, BglD1 and the mutant could be used as beneficial alternatives of the existing β-galactosidases for the production of GOS.