l-Asparaginase (E. C. 3. 5. 1. 1) is used as a therapeutic agent in the treatment of acute childhood lymphoblastic leukemia. It is found in a variety of organisms such as microbes, plants and mammals. In plants, l-asparaginase enzymes are required to catalyze the release of ammonia from asparagine, which is the main nitrogen-relocation molecule in these organisms. An Indian medicinal plant, Withania somnifera was reported as a novel source of l-asparaginase. l-Asparaginase from W. somnifera was cloned and overexpressed in E. coli. The enzymatic properties of the recombinant enzyme were investigated and the kinetic parameters (Km, kcat) for a number of substrates were determined. The kinetic parameters of selected substrates were determined at various pH and the pH- and temperature-dependence profiles were analyzed. WA gene successfully cloned into E. coli BL21 (DE3) showed high asparaginase activity with a specific activity of 17. 3 IU/mg protein. © 2011 The Author(s).
CITATION STYLE
Oza, V. P., Parmar, P. P., Patel, D. H., & Subramanian, R. B. (2011). Cloning, expression and characterization of l-asparaginase from Withania somnifera L. for large scale production. 3 Biotech, 1(1), 21–26. https://doi.org/10.1007/s13205-011-0003-y
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