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. 1972 Jun;23(6):1060–1066. doi: 10.1128/am.23.6.1060-1066.1972

Coupled-Enzyme System for Measuring Viral Neuraminidase Activity

Donald W Ziegler 1, Harriet D Hutchinson 1
PMCID: PMC380507  PMID: 4114435

Abstract

A coupled-enzyme assay for determining viral neuraminidase activity is described. All reactants—viral neuraminidase, the initial substrate (fetuin), N-acetylneuraminic acid aldolase, lactic acid dehydrogenase, and reduced nicotinamide adenine dinucleotide—are combined in a single cuvette. Thus, in a single coupled system neuraminidase releases N-acetylneuraminic acid, which is cleaved to N-acetyl-D-mannosamine and pyruvic acid; finally, pyruvate is reduced to lactate as reduced nicotinamide adenine dinucleotide is oxidized. The rate of change of absorbance at 340 nm, as reduced nicotinamide adenine dinucleotide is oxidized, is a measure of the rate of reaction of the coupled system. This procedure, which measures the rate of release of N-acetylneuraminic acid by neuraminidase, is an alternate method for those procedures which require multistep, colorimetric determinations.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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