 | Origami™
Origami host strains are K-12 derivatives that have mutations in both the thioredoxin reductase (trxB) and glutathione reductase (gor) genes, which together greatly enhance disulfide bond formation in the cytoplasm. Studies have shown that expression in Origami(DE3) yielded 10-fold more active protein than in another host even though overall expression levels were similar. Origami hosts are compatible with ampicillin-resistant plasmids and are ideal for use with pET-32 vectors, since the thioredoxin fusion tag further enhances the formation of disulfide bonds in the cytoplasm. The Origami(DE3)pLacI host is compatible with expression from pETBlue™ and pTriEx™ vectors. The trxB and gor mutations are selectable on kanamycin and tetracycline, respectively; therefore, these strains are recommended for use only with pET plasmids carrying the ampicillin resistance marker bla.
Origami B
Origami B host strains carry the same trxB/gor mutations as the original Origami strains, except that they are derived from a lacZY mutant of BL21. Thus the Origami B strains combine the desirable characteristics of 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 recommended for use only with pET plasmids carrying the ampicillin resistance marker bla.
Rosetta™
Rosetta host strains are Tuner™ derivatives designed to enhance the expression of eukaryotic proteins that contain codons rarely used in E. coli. These strains supply tRNAs for AGG, AGA, AUA, CUA, CCC, GGA codons on a compatible chloramphenicol-resistant plasmid. Thus the Rosetta strains provide for "universal" translation which is otherwise limited by the codon usage of E. coli. The tRNA genes are driven by their native promoters. In Rosetta(DE3)pLysS and Rosetta(DE3)pLacI, the rare tRNA genes are present on the same plasmids that carry the T7 lysozyme and lac repressor genes, respectively.
RosettaBlue™
RosettaBlue host strains are NovaBlue derivatives that combine high transformation efficiency and recA endA lacIq mutations with enhanced expression of eukaryotic proteins that contain codons rarely used in E. coli. These strains supply tRNAs for AGG, AGA, AUA, CUA, CCC, GGA codons on a compatible chloramphenicol-resistant plasmid. The tRNA genes are driven by their native promoters.
In RosettaBlue(DE3)pLysS and RosettaBlue(DE3)pLacI, the rare tRNA genes are present on the same plasmids that carry the T7 lysozyme and lac repressor genes, respectively. Blue/white screening is not possible with RosettaBlue(DE3) strains due to the presence of lacZ a-peptide coding sequences in the DE3 lysogenic phage. Rosetta-gami™
Rosetta-gami™ host strains are Origami™ derivatives that combine the enhanced disulfide bond formation resulting from trxB/gor mutations with enhanced expression of eukaryotic proteins that contain codons rarely used in E. coli. These strains supply tRNAs for AGG, AGA, AUA, CUA, CCC, GGA codons on a compatible chloramphenicol-resistant plasmid. The tRNA genes are driven by their native promoters. In Rosetta-gami(DE3)pLysS and Rosetta-gami(DE3)pLacI, the rare tRNA genes are present on the same plasmids that carry the T7 lysozyme and lac repressor genes, respectively. The trxB and gor mutations are selectable on kanamycin and tetracycline, respectively; therefore, these strains are recommended for use only with pET plasmids carrying the ampicillin resistance marker bla.
Rosetta-gami™ B
The Rosetta-gami™ B strains combine the key features of BL21 (and its Tuner™ derivative), Origami™, and Rosetta™ strains to enhance both the expression of eukaryotic proteins and the formation of target protein disulfide bonds in the bacterial cytoplasm.
All four Rosetta-gami B strains supply six different tRNAs to enable efficient translation of foreign transcripts that would otherwise be limited by the codon usage of E. coli. Rosetta-gami B strains also carry mutations in thioredoxin reductase (trxB) and glutathione reductase (gor) genes, which greatly enhances the formation of disulfide bonds in the cytoplasm. Deletion of the lac permease gene (lacY) allows adjustable, inducer (IPTG) dependent and uniform expression of target protein throughout all cells in a culture. Deficiencies in the lon and ompT proteases help to reduce proteolytic degradation.
Due to various selection requirements, these strains are not compatible with tetracycline, kanamycin or chloramphenicol resistant plasmids. Rosetta-gami B hosts are compatible with ampicillin-resistant plasmids and are ideal for use with pET-32 vectors, because the thioredoxin fusion tag further enhances the formation of disulfide bonds in the cytoplasm.
Tuner™
Tuner™ strains are lacZY deletion mutants of BL21 and enable adjustable levels of protein expression throughout all cells in a culture. The lac permease (lacY) mutation allows uniform entry of IPTG into all cells in the population, which produces a concentration-dependent, homogeneous level of induction. By adjusting the concentration of IPTG, expression can be regulated from very low level expression up to the robust, fully induced expression levels commonly associated with pET vectors. Lower level expression may enhance the solubility and activity of difficult target proteins. The Tuner(DE3)pLacI strain is compatible with expression from pETBlue™ and pTriEx™ vectors.
BL21
BL21 is the most widely used host background and has the advantage of being deficient in both lon (4) and ompT proteases. BL21trxB
BL21trxB strains possess the same thioredoxin reductase mutation (trxB) as the AD494 strains in the protease deficient BL21 background. Since trxB hosts facilitate cytoplasmic disulfide bond formation, their use may increase the fraction of properly folded protein (1). The trxB mutation is selectable on kanamycin; therefore, these strains are recommended for use only with plasmids carrying the ampicillin resistance marker bla.
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