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From three g of cell paste about a hundred mg of homogeneous protein ended up isolated. Enzymatic action was dependent on the presence of disulfide decreasing reagents for instance dithiothreitol or β-mercaptoethanol in the course of storage and purification. The indigenous molecular bodyweight in the purified enzyme was approximated to become one hundred eighty kDa centered on the elution quantity through a calibrated gel filtration column (data not demonstrated).
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