A Novel Agarolytic beta-Galactosidase Acts on Agarooligosaccharides for Complete Hydrolysis of Agarose into Monomers

Abstract

Marine red macroalgae have emerged to be renewable biomass for the production of chemicals and biofuels, because carbohydrates that form the major component of red macroalgae can be hydrolyzed into fermentable sugars. The main carbohydrate in red algae is agarose, and it is composed of D-galactose and 3,6-anhydro-L-galactose (AHG), which are alternately bonded by beta 1-4 and alpha 1-3 linkages. In this study, a novel beta-galactosidase that can act on agarooligosaccharides (AOSs) to release galactose was discovered in a marine bacterium (Vibrio sp.strain EJY3); the enzyme is annotated as Vibrio sp. EJY3 agarolytic beta-galactosidase (VejABG). Unlike the lacZ-encoded beta-galactosidase from Escherichia coli, VejABG does not hydrolyze common substrates like lactose and can act only on the galactose moiety at the nonreducing end of AOS. The optimum pH and temperature of VejABG on an agarotriose substrate were 7 and 35 degrees C, respectively. Its catalytic efficiency with agarotriose was also similar to that with agaropentaose or agaroheptaose. Since agarotriose lingers as the unreacted residual oligomer in the currently available saccharification system using beta-agarases and acid prehydrolysis, the agarotriose-hydrolyzing capability of this novel beta-galactosidase offers an enormous advantage in the saccharification of agarose or agar in red macroalgae for its use as a biomass feedstock for fermentable sugar production.