An efficient method to eliminate the protease activity contaminating commercial bovine pancreatic DNase I.

Anal Biochem

Department of Bioscience and Biotechnology, College of Natural Science, University of Suwon, Whasung City, Kyunggi-Do 445-743, Republic of Korea. Electronic address:

Published: August 2015

A method was developed to eliminate the proteases contaminating commercial DNase I, which can cause degradation of target protein during the purification process. Bio Basic DNase stock solution (in Tris-HCl buffer [pH 8.0] containing 5mM CaCl2) was first incubated at 50 °C to generate autolysis of proteases and zymogens, leading to a significant reduction in protease activity while preserving DNase activity. The residual protease activity was completely inhibited by further incubation with 2mM PMSF (phenylmethylsulfonyl fluoride) or 2× S8830 inhibitor cocktail. This approach could be readily applicable to eliminate the protease activity in any DNase products or during the preparation of commercial DNase.

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http://dx.doi.org/10.1016/j.ab.2015.04.030DOI Listing

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