In this work, four bacterial strains, BL21 (DE3), BL21 (DE3) pLysS, Rosetta, and Arctic Express, were chosen for parallel expression trials along with BL21 (DE3) complemented with folding chaperones DnaJ/K and GroEL/ES to compare their performance in producing soluble and active human kinases.
The four bcs-recombinant proteins were detected as the expected molecular weights in both induced cultures, but their overexpression was more pronounced in B21 (DE3) relative to DH5α cell lysates, in which no difference could be detected between induced and control culture profile. Given that BC is extracellularly expressed, it can be directly
BL21(DE3) Competent E.coli: C2527: 6 x 0.2ml: Agilent SURE2 Competent Cells: Agilent : 200152: 10 x 0.10ml: NEB Stable Competent E. coli (High Efficiency) C3040: 20 x 0.05ml: XL1-Blue MRF' Supercompetent Cells: Agilent: 200230: 5 x 0.2 mL: NEB Ā® Stable Competent E. coli (High Efficiency) C3040: 6 x 0.2 mL: BL21(DE3)pLysS Competent Cells
BL21, Tuner⢠and Origami hosts in one strain background. The trxB and gor mutations are selectable on kanamycin and tetracycline, respectively; therefore, these strains are recom-mended for use only with pET plasmids carrying the ampicillin resistance marker bla. Rosetta⢠Rosetta host strains are BL21 lacZY (Tunerā¢) derivatives designed
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difference between rosetta and bl21