Moore J T, Uppal A, Maley F, Maley G F
Wadsworth Center for Laboratories and Research, New York State Department of Health, Albany.
Protein Expr Purif. 1993 Apr;4(2):160-3. doi: 10.1006/prep.1993.1022.
Attempts at overexpressing T4-phage deoxycytidylate deaminase using the pET3c/BL21(DE3)/pLysS system resulted in this enzyme being part of an inactive inclusion-body complex. However, by employing an enriched growth medium it was found that the deaminase could be induced in a soluble active form to at least 20% of this organism's cellular protein. Insoluble inclusion bodies were obtained with less rich media. This procedure was employed successfully with other highly expressed proteins that formed inclusion bodies. The use of a rich growth medium during the course of protein induction may be a valuable adjunct to limiting inclusion body formation with this as well as other expression systems.
尝试使用pET3c/BL21(DE3)/pLysS系统过表达T4噬菌体脱氧胞苷酸脱氨酶,结果该酶成为无活性包涵体复合物的一部分。然而,通过使用富集生长培养基,发现脱氨酶可以以可溶性活性形式被诱导表达,其量至少占该生物体细胞蛋白的20%。使用营养成分较少的培养基则会形成不溶性包涵体。该方法已成功应用于其他形成包涵体的高表达蛋白。在蛋白质诱导过程中使用富集生长培养基,对于限制该表达系统以及其他表达系统中包涵体的形成可能是一种有价值的辅助手段。