Abstract:
:A membrane-bound xylose oxidizing PQQ-dependent dehydrogenase from Gluconobacter oxydans was purified with a simple large-scale applicable purification procedure. The activity recovery from membrane extract was 33% with 130-fold purification. Important characteristic with respect to the application of the dehydrogenase in biosensor technology were studied. The purified enzyme was most stable in the pH range 3.5-6.5. The pH optimum for xylose oxidation was in the range 7.5-8 for the solubilized enzyme. Optimal pH for the electrochemical detection of xylose oxidation was 6.5. Dimethyl and carboxylic acid derivatives of ferrocene were able to mediate electrons transferred in xylose oxidation from the enzyme immobilized on graphite electrode to the electrode. Hence the purified enzyme appeared to be suitable for biosensor applications.
journal_name
J Biotechnoljournal_title
Journal of biotechnologyauthors
Smolander M,Buchert J,Viikari Ldoi
10.1016/0168-1656(93)90060-zsubject
Has Abstractpub_date
1993-06-01 00:00:00pages
287-97issue
3eissn
0168-1656issn
1873-4863pii
0168-1656(93)90060-Zjournal_volume
29pub_type
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