Imobilization of [beta]-glucosidase using the cellulose-binding domain of Bacillus subtilis endo-[beta]-1,4-glucanase

A recombinant plasmid pβCBD was constructed for immobilization of Cellulomonas fimi β-glucosidase (Cbg) using the cellulose-binding domain (CBD) of Bacillus subtilis BSE 616 endo-β-1,4-glucanase (Beg). The Cbg-CBD ^sub Beg^ fusion protein, 80 kDa, was expressed in Escherichia coli and immobilized to...

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Veröffentlicht in:Biotechnology letters 1997-05, Vol.19 (5), p.483
Hauptverfasser: Ahn, Dong Ho, Kim, Hoon, Young Pack, Moo
Format: Artikel
Sprache:eng
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Zusammenfassung:A recombinant plasmid pβCBD was constructed for immobilization of Cellulomonas fimi β-glucosidase (Cbg) using the cellulose-binding domain (CBD) of Bacillus subtilis BSE 616 endo-β-1,4-glucanase (Beg). The Cbg-CBD ^sub Beg^ fusion protein, 80 kDa, was expressed in Escherichia coli and immobilized to Avicel. Cellobiose was completely hydrolyzed with the immobilized fusion protein. The fusion protein bound to Avicel retained full activity during continuous operation for 24 h at 4°C.[PUBLICATION ABSTRACT]
ISSN:0141-5492
1573-6776
DOI:10.1023/A:1018360530691