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. 2015 Nov 12;291(2):560–571. doi: 10.1074/jbc.M115.697524

TABLE 1.

Plasmids used in this work

Plasmid Description Reference
pUC19 E. coli cloning vector, AmpR, MCS Ref. 29
pUCB2 pUC19 /pUB110 shuttle vector, NeoR, PhleoR, AmpR Brantl (unpublished observations)
pUCBE1 pUCB2 with bsrE gene under own promoter and 96 bp upstream of − 35 box of pbsrE Footnote 4
pUCB5.1 pUCB2 with sr5 gene under own promoter and 87 bp upstream of − 35 box of psr5 Footnote 4
pUCBES2 pUCB5.1 with bsrE gene under own promoter and 96 bp upstream of − 35 box Footnote 4
pUCBES4 As pUCBES2, nt 51–163 of SR5 are lacking This study
pUCBES6 As pUCBES2, SR5 loop sequences of SL2 and SL4 exchanged by heterologous sequences This study
pUCBES7 As pUCBES2, nt 1–47, 91–104, and 126–163 of SR5 are lacking This study
pUCBES8 As pUCBES2, nt 49–78 of SR5 are lacking This study
pUCBES9 As pUCBES2, nt 1–46 and 105–163 of SR5 are lacking This study