Fractionation of the naringinase complex from Aspergillus terreus by dye affinity chromatography View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2004-08

AUTHORS

F. Soria, G. Ellenrieder, M. Grasselli, A.A. Navarro del Cañizo, O. Cascone

ABSTRACT

Affinity chromatography with immobilised triazine dyes was used to separate the main enzymes present in the naringinase complex produced by Aspergillus terreus CECT 2663. One alpha-L-rhamnosidase and two beta-D-glucosidases (beta G1 and beta G2) were separated by a simple two-step procedure involving chromatography with Red HE-3B immobilised on Sepharose 4B first at pH 5.5 and then at pH 4.7. Maximum activity of the beta-D-glucosidases was from pH 4 to 6 and at 65 degrees C. Both glucosidases were active on p -nitrophenol glucoside and prunin with respective Km values of 1.9 mm and 1.6 mm for beta G1 and 2.1 mm and 0.25 mm for beta G2. Only beta G1 hydrolysed cellobiose (Km = 5.7 mm). More... »

PAGES

1265-1268

Identifiers

URI

http://scigraph.springernature.com/pub.10.1023/b:bile.0000044870.99039.19

DOI

http://dx.doi.org/10.1023/b:bile.0000044870.99039.19

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1049907347

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/15483384


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