Search National Agricultural Library Digital Collections

NALDC Record Details:

Differential cellulolytic activity of native-form and C-terminal tagged-form cellulase derived from Coptotermes formosanus and expressed in E. coli

Permanent URL:
http://handle.nal.usda.gov/10113/34952
File:
Download [PDF File]
Abstract:
An endogenous cellulase gene (CfEG3a) of Coptotermes formosanus, an economically important pest termite, was cloned and overexpressed in both native form (nCfEG) and C-terminal His-tagged form (tCfEG) in Escherichia coli. Both forms of recombinant cellulases showed hydrolytic activity on cellulosic substrates. The nCfEG was more active and stable than tCfEG even though the latter could be purified to near homogeneity with a simple procedure. The differential activities of nCfEG and tCfEG were also evidenced by hydrolytic products they produced on different substrates. On CMC, both acted as an endoglucanase, randomly hydrolyzing internal β-1,4-glycosidic bonds and resulting in a smear of polymers with different lengths, although cellobiose, cellotriose, and cellotetraose equivalents were noticeable. The hydrolytic products of tCfEG were one unit sugar less than those produced by nCfEG. Using filter paper as substrate, however, the major hydrolytic products of nCfEG were cellobiose, cellotriose and trace of glucose; those of tCfEG were cellobiose, cellotriose and trace of cellotetraose, indicating a property similar to that of cellobiohydrolase, an exoglucanase. The results presented in this report uncovered the biochemical properties of the recombinant cellulase derived from the intact gene of Formosan subterranean termites. The recombinant cellulase would be useful in designing cellulase-inhibiting termiticides and incorporating into a sugar-based biofuel production program.
Author(s):
Zhang, Dunhua , Lax, Alan R. , Raina, Ashok K. , Bland, John M.
Subject(s):
insect pests , subterranean termites , Coptotermes formosanus , wood , cellulose , digestion , biochemical mechanisms , enzymes , cellulases , enzymatic hydrolysis , enzyme activity , insect genetics , genes , gene expression , in vitro studies , Escherichia coli , gene overexpression , terminal repeat sequences , insect control , biological control , genetic recombination
Format:
p. 516-522.
Note:
Includes references
Source:
Insect biochemistry and molecular biology 2009 Aug., v. 39, issue 8
Language:
English
Year:
2009
Collection:
Journal Articles, USDA Authors, Peer-Reviewed
Rights:
Works produced by employees of the U.S. Government as part of their official duties are not copyrighted within the U.S. The content of this document is not copyrighted.