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. 2004 Mar;186(6):1811–1817. doi: 10.1128/JB.186.6.1811-1817.2004

TABLE 1.

Bacterial strains and plasmids used in this study

Strain or plasmid Descriptiona Source
E. coli
    DH5α Host for cloning vectors Life Technologies
    BL21 DE3/pLysE Host for protein synthesis, Camr Novagen
    JMSB0338 BL21 DE3/pLysE containing pJMSB0338; Ampr Camr This work
S. enterica serovar Typhimurium
    TR6579 Shuttle vector between E. coli and S. enterica serovar Typhimurium LT2 J. R. Roth
    RMC26 dxs::mevalonate operon (araC Pbad erg8 erg12 erg19 Kanr) C. A. Testa
    RMC29 RMC26 with idi::Camr This work
    TT22236 S. enterica serovar Typhimurium (LT2) cbiD24::MudJ containing pTP223 J. R. Roth
    JMSB0351 RMC29 containing pJMSB0338 This work
    JMSB0354 RMC29 containing pBAD Myc/HisA This work
Plasmids
    pGEM-T Easy Cloning vector for PCR products; Ampr Promega
    pBAD Myc/His A E. coli expression vector; Ampr Invitrogen
    pJMSB0335 pGEM-T Easy with a 1.1-kb BgIII-HindIII fragment corresponding to bp 26230 through 27279 in the M. thermautotrophicus genome (ORF48) This work
    pJMSB0338 pBAD Myc/His A with a 1.1-kb BgIII-HindIII fragment containing ORF48 This work
    pTP223 lam, bet, and exo genes of phage lambda expressed from a lac promoter A. R. Poteete and A. C. Fenton
a

Camr, chloramphenicol resistance; Ampr, ampicillin resistance.