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. 1999 Sep;65(9):4032–4039. doi: 10.1128/aem.65.9.4032-4039.1999

TABLE 1.

B. thuringiensis strains and plasmids

Strain or plasmid Relevant genotype or plasmid characteristics Reference(s)
407 Acrystalliferous derivative of the wild-type B. thuringiensis strain 407 (H1 serotype) isolated by O. Arantes 3, 18
Kto (HD73) Wild-type B. thuringiensis strain containing Tn4430 and a cry1Ac gene 15, 31
Kto Acrystalliferous derivative of the wild-type B. thuringiensis strain Kto 31
407(pHTF3-1C) Cry1C δ-endotoxin produced in the 407 background This report
407(pHTF3-1C/Ab) Cry1C/Ab chimeric δ-endotoxin produced in the 407 background This report
AGRO2 Kto strain electrotransformed with plasmid pHTF3-1C/Ab-IRS-T and containing pHTF3-1C/Ab-IRS-T-Δ as a result of site-specific recombination in vivo This report
Kto SigK Kto strain whose sigK gene was disrupted by the insertion (by homologous recombination) into the chromosome of a sigK gene interrupted by the aphA3 kanamycin resistance gene (sigK::aphA3) This report
AGRO1 Kto SigK strain containing pHTF3-1C/Ab-IRS-T-Δ as a result of site-specific recombination in vivo after electrotransformation of the host strain with pHTF3-1C/Ab-IRS-T This report
pAB2 Plasmid containing the sigK gene of B. thuringiensis strain 407 disrupted by the aphA3 gene of E. faecalis, cloned into pRN5101 7
pHT81 Plasmid containing a chimeric cry1C/Ab gene, consisting of the 5′ end region of the cry1C gene fused (at the KpnI site) to the 3′ end region of the cry1Ab gene, cloned in pUC19 29
pHTF3-1C Plasmid consisting of the coding sequence of the cry1C gene fused to the sporulation-independent cry3A promoter inserted into pHT315 (3) 30
pHTF3-1C/Ab Plasmid consisting of the coding sequence of the chimeric cry1C/Ab gene fused to the cry3A promoter and inserted into pHT315 (3) This report
pHTBS2 Plasmid containing the origin of replication of the B. thuringiensis resident plasmid pHT1030 and the tetracycline resistance gene carried by pBC16 of B. cereus cloned into pBluescript II KS(−) 30
pHT-IRS-BSK Plasmid consisting of the pBluescript II KS(−), the aphA3 gene of E. faecalis, and one copy of the IRS of Tn4430 31
pHTF3-1C/Ab-IRS-K and pHTF3-1C/Ab-IRS-T Site-specific recombination vectors consisting of the pBluescript II KS(−) and the kanamycin resistance gene aphA3 of E. faecalis (pHTF3-1C/Ab-IRS-K) or the tetracycline resistance gene carried by pBC16 of B. cereus (pHTF3-1C/Ab-IRS-T) between duplicated copies of the IRS of transposon Tn4430 and segregated from the native B. thuringiensis plasmid components: the chimeric cry1C/Ab gene under the control of the cry3A promoter and the replication and stability regions of plasmid pHT1030 This report