Difference between revisions of "PGP886"
| Line 7: | Line 7: | ||
*An additional base has to be inserted in the forward primer to restore the frame. | *An additional base has to be inserted in the forward primer to restore the frame. | ||
*Don't forget a stop codon in the reverse primer. | *Don't forget a stop codon in the reverse primer. | ||
| − | <pubmed> 24493247 </pubmed> | + | |
| + | <pubmed>24493247</pubmed> | ||
== Return to [[Plasmids]] == | == Return to [[Plasmids]] == | ||
Latest revision as of 15:26, 6 February 2014
The vector was constructed in Jörg Stülke's lab and it is suitable for the xylose-inducible expression of proteins in B. subtilis. The plasmid confers resistance to ampicillin and erythromycin/lincomycin in E. coli and B. subtilis, respectively. To transform B. subtilis, the plasmid has to be linearized with ScaI or NotI. The plasmid will integrate into the xkdE gene.
Hints for usage
- An additional base has to be inserted in the forward primer to restore the frame.
- Don't forget a stop codon in the reverse primer.
Jan Gerwig, Taryn B Kiley, Katrin Gunka, Nicola Stanley-Wall, Jörg Stülke
The protein tyrosine kinases EpsB and PtkA differentially affect biofilm formation in Bacillus subtilis.
Microbiology (Reading): 2014, 160(Pt 4);682-691
[PubMed:24493247]
[WorldCat.org]
[DOI]
(I p)
