Abstract
A 5.8 kbp DNA fragment from Clostridium cellulovorans (ATCC 35296) containing endo-β-1,4-glucanase (1,4-β-d-glucan glucanohydrolase, carboxymethylcellulase, CMCase; EC 3.2.1.4) gene, engD was cloned in Escherichia coli. The clone harboring a subcloned 3.8 kb fragment in plasmid, pEQ52V, produced an enzyme that showed both endo-β-1,4-glucanase activity as well as cellobiosidase activity. Zymograms with the engD encoded enzyme with carboxymethyl-cellulose as the substrate indicated that the molecular mass of the active protein was 50 000.
Original language | English |
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Pages (from-to) | 285-288 |
Number of pages | 4 |
Journal | FEMS Microbiology Letters |
Volume | 72 |
Issue number | 3 |
DOIs | |
State | Published - Nov 1990 |
Externally published | Yes |
Bibliographical note
Funding Information:The research was supported in part by Department of Energy Grant DE-FG03-87ERI3705. O.S. was supported by Fellowship SI-0057-87 from the United States-Israel Binational Agricultural Research and Development Fund.
Keywords
- Cellobiosidase
- Clostridium cellulovorans
- Endoglucanase
- Molecular cloning