SSSAJ Journal of Natural Resources and Life Sciences Education
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Published online 2 February 2006
Published in Soil Sci Soc Am J 70:378-381 (2006)
DOI: 10.2136/sssaj2005.0156N
© 2006 Soil Science Society of America
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Soil Biology and Biochemistry Note

Automated Robotic Assay of Phosphomonoesterase Activity in Soils

M. J. Sadowskya,*, W. C. Koskinenb, J. Seebingerc, B. L. Barberc and E. Kandelerd

a Dep. of Soil, Water, & Climate, and BioTechnology Institute, Univ. of Minnesota, St. Paul, MN 55108, USA
b USDA-ARS, Soil and Water Management Research Unit, St. Paul, MN 55108, USA
c Dep. of Soil, Water, & Climate, Univ. of Minnesota, St. Paul, MN 55108, USA
d Institute of Soil Science and Land Evaluation, Univ. of Hohenheim, 70599 Stuttgart, Germany

* Corresponding author (Sadowsky{at}umn.edu)

Phosphorus cycling in most ecosystems is dependent on plant and microbiologically derived phosphatase enzymes, and available P limits both microbial and plant growth. Measurements of enzymes in soil systems are often time-consuming and labor intensive. In this study, we examined phosphomonoesterase activity in soils using a Zymark XP laboratory robotic system for soil handling, solvent addition and exchange, filtration, incubation, reagent addition, and final sample preparation. Phosphomonoesterase activity was measured using phenyl phosphate as substrate, and samples were analyzed using a 96-well microplate reader. Results indicated that our robotic system was capable of effectively measuring phosphomonoesterase activity in soils differing in physical and chemical characteristics. The results obtained using manual and robotic procedures were comparable in accuracy and precision. The robotic system decreased labor associated with this assay by about a factor of 4.5 relative to the manual system, with considerable savings on reagent costs and labor.




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Appl. Environ. Microbiol.Home page
T. Yan, M. J. Hamilton, and M. J. Sadowsky
High-Throughput and Quantitative Procedure for Determining Sources of Escherichia coli in Waterways by Using Host-Specific DNA Marker Genes
Appl. Envir. Microbiol., February 1, 2007; 73(3): 890 - 896.
[Abstract] [Full Text] [PDF]




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