The main goal of this work was to evaluate the performance of beta-galactosidase from Exiguobacterium acetylicum MF03 in both hydrolysis and transgalactosylation reactions from different substrates. The enzyme gene was expressed in Escherichia coli BL21 (DE3), sequenced, and subjected to bioinformatic and kinetic assessment. Results showed that the enzyme was able to hydrolyze lactulose and o-nitrophenyl-beta-D-galactopyranoside, but unable to hydrolyze lactose, o-nitrophenyl-beta-D-glucopyranoside, butyl-and pentyl-beta-D-galactosides. This unique and novel substrate specificity converts the E. acetylicum MF03 beta-galactosidase into an ideal catalyst for the formulation of an enzymatic kit for lactulose quantification in thermally processed milk. This is because costly steps to eliminate glucose (resulting from hydrolysis of lactose when a customary beta-galactosidase is used) can be avoided.