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. Author manuscript; available in PMC: 2012 Oct 4.
Published in final edited form as: J Biol Chem. 2005 Oct 31;281(2):1119–1127. doi: 10.1074/jbc.M509421200

TABLE 1.

Bacterial strains, plasmids, and promoters used in this work

Brief description Source/Ref.
Bacterial strains
HB101
M182 Δ(lacIPOZY) × 74galK galU strA Ref. 46
UQ3259 Fhis StrR relA1 ilv∷Tn10 cya (SA2755) S. Adhya
UQ3260 Fhis StrR relA1 crpcam (SA2777) S. Adhya
UQ3261 Fhis StrR relA1 ilv∷Tn10 cya and crpcam This work
UQ3588 HB101 with ilv∷Tn10 cya and crpcam recA56 TnR This work
UQ3740 M182 carrying λ prophage with CC(−41.5)∷lacZ fusion (RLG4649) Ref. 26
UQ3741 M182 carrying λ prophage with CC(−61.5)∷lacZ fusion (RLG4650) Ref. 27
UQ3809 UQ3740 with ilv∷Tn10 cya and crpcam This work
UQ3811 UQ3741 with ilv∷Tn10 cya and crpcam This work

Plasmids
pEXT20 Ref. 32
pHY26-1 pEXT20 plasmid bearing E. coli crp allele (His6-tagged) This work

Promoters
pSR pBR322 derivative containing λ OOP transcription terminator Ref. 47
pSR/CC(−41.5) Class II derivative of melR promoter with consensus CRP-binding site centered at −41.5 Ref. 26
pSR/CC(−61.5) Class I derivative of melR promoter with consensus CRP-binding site centered at −61.5 Ref. 27