Skip to main content
Log in

A note on the estimation of microbial glycosidase activities by dinitrosalicylic acid reagent

  • SHORT CONTRIBUTION
  • Published:
Applied Microbiology and Biotechnology Aims and scope Submit manuscript

Abstract

 In the estimation of glycosidase activity by dinitrosalicylic acid (DNS) reagent, the stoichiometry of DNS reduction was reported to increase proportionately with the increase in the number of glycosidic linkages present in oligosaccharides liberated by the enzyme. The relationship between increases in DNS reduction and increases in the number of glycosidic bonds was found to be represented by a part of a rectangular hyperbola. The increase was optimum with disaccharide and insignificant when the degree of polymerization (DP) was ≥10. The difference did not arise as a result of the DNSA discriminating between mono- and oligosaccharide oxidation. The relationship stemmed from the acidity of the hydroxyl group adjacent to the reducing group, which repressed DNS reduction. The acidity is likely to decrease with an increase in oligosaccharide chain length. It is suggested that DNS reduction is actually optimum and uniform for all oligosaccharides of DP ≥ 10 and that it is minimum for monosaccharide. Thus the introduction of rectification factors in the estimation of glycosidase activities by the DNS method appears to be justified.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Additional information

Received: 18 January 1999 / Received revision: 7 December 1999 / Accepted: 19 December 1999

Rights and permissions

Reprints and permissions

About this article

Cite this article

Sengupta, S., Jana, M., Sengupta, D. et al. A note on the estimation of microbial glycosidase activities by dinitrosalicylic acid reagent. Appl Microbiol Biotechnol 53, 732–735 (2000). https://doi.org/10.1007/s002530000327

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s002530000327

Keywords

Navigation