This study screens 50 fungal strains for β-galactosidase activity (agar X-gal plate), then validates 8 strains in submerged lactose fermentation and tests their crude extracts for lactulose + GOS synthesis (lactose+fructose) and (in some cases) FOS production via fructosyltransferase activity (lactose+sucrose). The headline claim—simultaneous generation of mixed prebiotic families from crude dual-activity extracts—is supported by their HPLC-based sugar profiles and reported titers/yields, but it remains limited by the use of crude enzyme mixtures, non-optimized reaction conditions, and inference of product identity mainly via retention time and standards rather than full linkage-structure verification.
Their validation step reports strong β-galactosidase activities for several strains (e.g., A. uvarum and T. versicolor are highest among those summarized). These quantities are consistent with a true enzymatic signal, not just plate color.
Under lactose+fructose incubation, they report maximal lactulose and GOS titers across strains, with representative time-to-max and lactose conversion patterns.
β-galactosidases commonly catalyze both hydrolysis and transglycosylation depending on reaction conditions and enzyme properties; broadly, this supports why lactose-based transgalactosylation products (GOS, lactulose) are feasible from β-galactosidase-containing preparations.
Their conclusion that dual-activity enables simultaneous GOS+lactulose+FOS production relies on crude mixtures that likely contain multiple enzymatic activities. They explicitly report that hydrolysis/transgalactosylation of both lactose and sucrose is “evidence of lack of purity” of extracts. This makes attribution to a single enzyme difficult (e.g., what fraction of observed FOS is from a specific FFase cofactor vs contaminating activities).
The paper interprets product classes (e.g., “mainly trisaccharides”) using HPLC retention time behavior compared against standards/mix standards. While this is standard practice, it doesn’t automatically guarantee linkage-level or isomer-level identity for all product species, especially in complex crude backgrounds.
They acknowledge that enzyme concentrations (U/L) differ across strains and that their crude-extract “simple approach” needs optimization and/or purification to better compare biocatalyst potential. More generally, the prebiotic field shows that yields depend strongly on enzyme/conditions and the transglycosylation vs hydrolysis balance.
They report that for some extracts lactulose/GOS concentrations decrease after reaching maxima and propose secondary hydrolysis as a cause. This is a plausible explanation, but it also means “max product titers” may be time-dependent and enzyme-mixture-dependent, not solely governed by transglycosylation efficiency.
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