Abstract
A commercially available β-glucosidase (β-D-glueoside glucohydrolase, E. C. 3.2.1.21) preparation was investigated as a possible alternative to a more expensive commercial chitobiase (chitobiose acetylaminodeoxyglucohydrolase, E. C. 3.2.1.29) for use in chitinase assay. The preparation hydrolyzed N,N 1 -diacetylchitobiose at a rate comparable to the chitobiase, but also hydrolyzed chitin substrates. Regenerated chitin was hydrolyzed to a greater extent with the β-glucosidase preparation alone than when soybean chitinase (chitin glycanohydrolase, E. C. 3.2.1.14) was also included in the reaction. Activity decreased with additional amounts of chitinase in the assay, indicating a competition between the two preparations for the substrate. The β-glucosidase itself may hydrolyze regenerated chitin to a certain extent. The β-glucosidase alone also hydrolyzed microcrystalline chitin and crab shell chitin, with release of N-acetylglucosamine, suggesting the presence of a contaminating chitinase in the β-glucosidase preparation. Further study is indicated in order to determine the limitations of the use of β-glucosidase preparations as sources of chitobiase activity in chitinase assay systems.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.