Publication Cover
Journal of Environmental Science and Health, Part A
Toxic/Hazardous Substances and Environmental Engineering
Volume 47, 2012 - Issue 13
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ARTICLES

Nitrate reduction by commercially available nitrate reductases: Bio-catalytic potentials and enzymatic activities in the presence of metals ions

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Pages 2028-2034 | Received 19 Jan 2012, Published online: 07 Aug 2012
 

Abstract

Commercially available nitrate reductases from corn, Aspergillus niger, and Escherichia coli have the potential to mitigate excess nitrate in soils and water sources. In this study, in vitro experiments were conducted to evaluate nitrate reduction by commercially available nitrate reductases from three major sources (plant, fungi and bacteria), their biocatalytic potentials and activities in the presence of varied concentrations of Cd2+, Cu2+, Ni2+, Co2+, Cr6+, Fe2+, Zn2+, and Pb2+. The results showed that the activity, V max, and potential to reduce nitrate was in the order: corn > A. niger > E. coli. The kinetic constant (K m) based on the various substrates used demonstrated that the binding affinity was generally highest for E. coli and lowest for A. niger. Based on the specificity constants obtained in this study, nitrate reductase from corn was the most efficient of all the enzymes assayed, yet that from E. coli showed the least. Nitrate reductase from corn and A. niger showed more variations with increase in metal ions concentrations compared to E. coli (with the exception of Cu2+). Information reported in this study will enable the assessment of the contributions and sources of nitrate reductases in mitigating environmental and health issues resulting from nitrate pollution.

Acknowledgments

This work is a contribution of the Winfred Thomas Agricultural Research Station, Alabama A&M University, Normal, AL. Trade or manufacturers’ names mentioned are for information only and do not constitute endorsement, recommendation, or exclusion by Alabama A&M University. This research was supported in part by USDA-CSREES, Evans-Allen Grant # ALAX 011.

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