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. 2009 Oct 14;4(10):e7462. doi: 10.1371/journal.pone.0007462

Table 4. Bacterial strains and plasmids used in this study.

Designation Characteristics/genotype Source/Reference
A. Bacterial strains
 E. coli ET12567/pUZ8002 Non-methylating plasmid donor for intergeneric conjugation with Streptomyces [60]
 S. antibioticus IMRU 3720 Wild type [57]
  YU5 ΔmelC mutant [10]
 YU5-117 YU5 containing pSET152-117 inserted at the ΦC31 attB site This study
 S. avermitilis Wild type Haruo Ikeda
  B19 ΔmelC mutant This study
 S. coelicolor A3 (2)
 M145 Prototrophic, SCP1 SCP2 [59]
 HY2 M145 with a his6-tagged melD2 This study
 HY69 ΔmelD mutant of M145 This study
 S. lipmanii ATCC 27357 Wild type CCRC*
 S. lividans 1326 Wild type, SLP2+, SLP3+ [58]
 S. maritimus Wild type [55]
 S. tanashiensis ATCC 23967 Wild type [55]
 S. rochei 7434-AN4 Wild type [56]
B. Plasmids
 pIJ702-117 Derivative of pIJ702 containing melC of S. antibioticus under a strong promoter [27]
 pSET152-117 Derivative of pSET152 containing melC of pIJ702-117 This study
 pLUS702melD pIJ702-117 with melC substituted by melD and an inserted aac 3(IV) This study
 pCR2.1TOPO E. coli cloning vectors, kanamycin and ampicillin resistance, lacZ α Invitrogen
*

Culture Collection and Research Center (CCRC), Food Industry Research and Development Institute, Hsinchu, Taiwan