Amidase Activity in Soils: II. Kinetic Parameters
- 1 May 1980
- journal article
- research article
- Published by Wiley in Soil Science Society of America Journal
- Vol. 44 (3) , 532-536
- https://doi.org/10.2136/sssaj1980.03615995004400030019x
Abstract
Studies to determine the kinetic parameters of the amidasecatalyzed reaction in soils showed that the Km values of formamide, acetamide, and propionamide for this enzyme are similar to those of the same enzyme isolated from microorganisms. Application of the three linear transformations of the Michaelis‐Menten equation indicated that the apparent Km constants of the three substrates (formamide, acetamide, and propionamide) varied among the soils studied, but the results obtained by the three plots were similar. By using the Lineweaver‐Burk plot, the Km values of formamide, acetamide, and propionamide in eight soils ranged from 6.7 to 17.9mM (avg. 12.3), 4.0 to 5.1mM (avg. 4.6), and 10.1 to 20.2mM (avg. 14.5), respectively. The Km value is the lowest and affinity constant is the highest at optimum pH of amidase activity. With the substrate used in parentheses, the Vmax values of the eight soils ranged from 138 to 438 µg NH4‐N released/g soil per 24 hours (formamide), from 13 to 43 µg NH4‐N released/g soil per 24 hours (acetamide), and from 35 to 105 µg NH4‐N released/g soil per 24 hours (propionamide). The activation energy values for the amidase activity, expressed in kJ/mol, ranged from 43.3 to 49.8 (avg. 46.9), from 43.2 to 55.5 (avg. 50.0), and from 22.6 to 29.8 (avg. 26.5) using formamide, acetamide, and propionamide as substrates, respectively. The average temperature coefficient (Q10) of the amidase‐catalyzed reaction in the eight soils studied for temperature ranging from 10 to 60°C was 1.70 for formamide, 1.73 for acetamide, and 1.42 for propionamide.Keywords
This publication has 5 references indexed in Scilit:
- Phosphodiesterase Activity of SoilsSoil Science Society of America Journal, 1978
- The kinetics of soil acid phosphataseSoil Biology and Biochemistry, 1976
- The Aliphatic Amidases of Pseudomonas aeruginosaPublished by Elsevier ,1969
- A Comparison of Estimates of Michaelis-Menten Kinetic Constants from Various Linear TransformationsJournal of Biological Chemistry, 1965
- REACTIONS CATALYZED BY AMIDASES - ACETAMIDASE1964