Double-Antibody Sandwich Enzyme-Linked Immunosorbent Assay for Cellobiohydrolase I

Author:

Riske Frank J.1,Eveleigh Douglas E.1,Macmillan James D.1

Affiliation:

1. Department of Biochemistry and Microbiology, Cook College, Rutgers University, P. O. Box 231, New Brunswick, New Jersey 08903

Abstract

A double-antibody sandwich enzyme-linked immunosorbent assay was developed for quantifying cellobiohydrolase I (CBH I) in crude preparations of the cellulase complex from Trichoderma reesei. The other enzymes (endoglucanase and β-glucosidase) in this complex and other ingredients in culture broth did not interfere with this assay. The antibody configuration that resulted in the highest specificity for the assay of CBH I employed a monoclonal antibody to coat wells in polystyrene plates and peroxidase-labeled polyclonal antibody to detect cellobiohydrolase bound to the immobilized monoclonal antibody. Previously, procedures have not been available for the direct assay of CBH I activity in the presence of the other enzymes in the complex, and current indirect procedures are cumbersome and inaccurate. The direct procedure described here is highly specific for CBH I and useful for quantifying this enzyme in the range of 0.1 to 0.8 μg/ml.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

Reference30 articles.

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4. Claeyssens M. 1988. The use of chromophoric substrates and specific assays in the study of structure-activity relationships of cellulolytic enzymes p. 393-397. In J.-P. Aubert P. Beguin and J. Millet (ed.) FEMS Symposium No. 43. Biochemistry and genetic of cellulose degradation. Academic Press Inc. (London) Ltd. London.

5. An assay for the selective determination of exo-1,4-0-glucanases in a mixture of cellulolytic enzymes;Deshpande M. K.;Anal. Biochem.,1984

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