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PMID: 2840356 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Cloning and expression of two cellulase genes of Clostridium cellulolyticum in Escherichia coli.

Gene ·Vol. 65 ·No. 1 ·1988-05-15 ·Pages 51-8

Faure E, Bagnara C, Belaich A, Belaich JP

Abstract

Two cellulase genes isolated from Clostridium cellulolyticum strain ATCC3519 were cloned in Escherichia coli using plasmid pACYC184. Plasmids pB52 and pB43 were isolated from the transformants producing carboxymethylcellulase (CMCase) and the two cloned CMCase-coding genes were found to be included in two EcoRI fragments of 5.7 kb and 2.6 kb, respectively. These two genes showed no homology. The CMCase-coding genes were found to be contained in a 1.8-kb KpnI-HindIII fragment and a 2.05-kb HindIII-PvuII fragment of the DNA donor strain. Expression of these genes in E. coli was found not to depend on their orientation in the cloning vector. Hybridization experiments between these two fragments and Clostridium thermocellum NCIB10682 DNA fragments carrying genes celA, celB, celC and celD were carried out and some homologies were detected.

MeSH Terms
Cellulase/genetics Cloning, Molecular Clostridium/enzymology,genetics DNA Restriction Enzymes Escherichia coli/genetics Genes Genes, Bacterial Nucleic Acid Hybridization Nucleotide Mapping Plasmids Species Specificity Transcription, Genetic
Chemicals
DNA Restriction Enzymes Cellulase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Faure E
Laboratoire de Chimie Bactérienne, Centre National de la Recherche Scientifique, Marseille, France.
Bagnara C
Belaich A
Belaich J P
Article Info
Journal
Gene
Abbr.
Gene
ISSN
0378-1119
Published
1988-05-15
Pages
51-8
Language
English
Region
Netherlands
NLM ID
7706761
Subset
IM
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