Abstract
Functional screening studies revealed that Aspergillus carbonarius ATCC6276 produced extracellular β-galactosidase activity potentially suited for use as a lactase digestive supplement in the treatment of lactose intolerance. The crude preparation contained two β-galactosidase activities, β-gal 1 and β-gal 2, which were separated by ion-exchange chromatography. Both enzymes were purified to homogeneity by a combination of gel filtration, ion-exchange, chromatofocusing and hydrophobic interaction chromatographies. β-gal 1 and β-gal 2 displayed differences in molecular mass (110 kDa versus 120 kDa as judged by SDS PAGE) and in a range of additional physicochemical properties. Km values of 83 and 309 mM, respectively, were recorded using lactose as substrate while temperature optima of 55°C versus 65°C were obtained. Unlike current commercialized supplemental lactases, both of the purified enzymes displayed significant stability when exposed to simulated gastric conditions, with β-gal 1in particular retaining 70% residual activity after exposure to pH 2.0 in the presence of pepsin for 2 h. Overall the results indicate that the β-galactosidases of Aspergillus carbonarius ATCC6276, either individually or in combination, may be suitable for use as a digestive supplement for the alleviation of lactose intolerance.
| Original language | English |
|---|---|
| Pages (from-to) | 129-138 |
| Number of pages | 10 |
| Journal | Applied Biochemistry and Biotechnology |
| Volume | 149 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - May 2008 |
Keywords
- Aspergillus carbonarius
- Lactase
- Lactose intolerance
- β-galactosidase
Fingerprint
Dive into the research topics of 'Application relevant studies of fungal β-galactosidases with potential application in the alleviation of lactose intolerance'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver