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. 2011 Jul 20;11:164. doi: 10.1186/1471-2180-11-164

Table 2.

Strains and plasmids used in this study

Strains or plasmids relevant characteristics Source or reference
Strains
S. ansochromogenes 7100 Wild-type strain [40]
sabRDM The sabR disruption mutant [24]
E. coli DH5α F- recA f80 dlacZ ΔM15 Gibco BRL
BL21(DE3) F- ompT hsdS gal dcm (DE3) Novagen
ET12567 (pUZ8002) recE dam dcm hsdS Cmr Strr Tetr Kmr [41]
Alternaria longipes Indicator strain for nikkomycin bioassays [40]
Plasmids
pBluescript KS+ Routine cloning and subcloning vector Stratagene
pET23b Expression vector Novagen
pET23b::sabR sabR gene cloned in pET23b This work
pIJ8600 ori pUC, oriT RK2, int ΦC31, tipAp, tsr, aprR [33]
pIJ8600::sabR sabR gene cloned in the induced vector of pIJ8600 which containing PtipA as promoter This work
pKC1139 E.coli-Streptomyces shuttle vector [33]
pGARE1 A 974 bp DNA fragment containing the left flank of SARE was inserted into pUC119::kan This work
pGARE2 A 806 bp DNA fragment containing the right flank of SARE was inserted into GAREL1 This work
pGARE3 A 2.8 kb DNA fragment containing the left and right flanks of SARE and kanamycin resistance gene from pGARE2 was inserted into pKC1139 This work
pGARE4 The 1 kb kanamycin resistance gene was deleted from pGARE3 This work
pGARE5 A 1.8 kb DNA fragment containing the left and right flanks of SARE from pGARE4 was inserted into pKC1139 This work