Skip to main content
. 1998 Jul;180(13):3353–3359. doi: 10.1128/jb.180.13.3353-3359.1998

TABLE 1.

Bacterial strains and plasmids used in this study

Strain or plasmid Description Reference
E. coli
 DH5α F′ φ80dlacZΔM15 endA1 recA1 gyrA96 thi-1 hsdR17(rK mK+) supE44 relA1 deoR Δ(lacZYA-argF)U169 9
 InvαF′ F′ endA1 recA1 hsdR17(rK mK+) supE44 thi-1 gyrA96 relA1 φ80lacZΔM15 Δ(lacZYA-argF)U169 Invitrogen
N. europaea
 ATCC 19178 American Type Culture Collection
 A141 Insertion of lacZ/kan into the BamHI site of amoA1 This study
 A142 Insertion of lacZ/kan into the BamHI site of amoA2 This study
 A1 Insertion of kan into the BamHI site of amoA1 This study
 A2 Insertion of kan into the BamHI site of amoA2 This study
Plasmids
 pNHA10 842-bp PCR fragment containing most of amoA cloned into pCRII vector This study
 pNHA11 pNHA10 with a mutation in amoA at position 715 (24), creating a BamHI site This study
 pNHA12 amoA insert cut out of pNHA11 with EcoRI and cloned into EcoRI site of pRL139 This study
 pNHA14 lacZ/kan fragment from pKOK6.1 inserted into BamHI site of pNHA12 This study
 pNHA15 kan from pUC4 pKSAC inserted into BamHI site of pNHA12 This study
 pUC4 KSAC Plasmid containing the kan cassette from Tn903 Pharmacia
 pKOK6.1 Plasmid containing a promoterless lacZ and kan with its own promoter 20
 pCRII TA PCR cloning vector (Kanr AmprlacZa f1ori ColE1 ori) Invitrogen
 pRL139 pUC19 with a symmetrical multiple cloning site 5