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Expression, high cell density culture and purification of recombinant EC-SOD in Escherichia coli.

Appl Biochem Biotechnol.. 2010-11;  162(6):1585-1598
Son YJ, Bae JY, Chong SH, Lee HS, Mo SH, Kim TY, Choe H. Department of Physiology and Research Institute for Biomacromolecules, University of Ulsan College of Medicine, 388-1 PoongNap-dong, Songpa-goo, Seoul, South Korea.
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摘要

Superoxide dismutase (SOD) catalyzes the dismutation of the biologically toxic superoxide anion into oxygen and hydrogen peroxide and is deployed by the immune system to kill invading microorganisms. Extracellular SOD (EC-SOD) is a copper- and zinc-containing glycoprotein found predominantly in the soluble extracellular compartment that consists of approximately 30-kDa subunits. Here, we purified recombinant EC-SOD3 (rEC-SOD) from Escherichia coli BL21(DE3) expressing a pET-SOD3-1 construct. Cells were cultured by high-density fed-batch fermentation to a final OD(600) of 51.8, yielding a final dry cell weight of 17.6 g/L. rEC-SOD, which was expressed as an inclusion body, comprised 48.7% of total protein. rEC-S... More

关键词

rEC-SOD; Fermentation; Refolding; Purification; MALDI-TOF