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. 2000 Oct;66(10):4300–4304. doi: 10.1128/aem.66.10.4300-4304.2000

TABLE 1.

Bacterial strains and plasmids used in this study

Strain or plasmid Description Reference or source
Strains
Mycobacterium sp. strain PYR-1 Mineralizes high-molecular-weight PAHs such as fluoranthene, pyrene, and phenanthrene 8
Escherichia coli XL1-Blue MRF′ lac [F′ proAB lacIqZΔM15 Tn10 (Tetr)] Stratagene
Escherichia coli XLOLR lac [F′ proAB lacIqZΔM15 Tn10 (Tetr)] Su (nonsuppressing) λr Stratagene
Escherichia coli TOP10 One Shot competent cells, F′ mcrA Δ(mmr-hsdRMS-mcrBC) Φ80lacZΔM15 Δ(ara-leu)7697 Invitrogen
Plasmid or vector
 ExAssist helper phage For in vivo excision of the pBK-CMV phagemid from the ZAP Express vector with E. coli XLOLR Stratagene
 Zap Express vector Lambda vector, prokaryotic and eukaryotic expression, in vivo excision of the pBK-CMV vector Stratagene
 pBK-CMV vector Neor Kanr, ColE1 origin, lacZ, cytomegalovirus promoter Stratagene
 Myco-pBK-CMV phagemid pBK-CMV phagemid with 1.8-kb insert from Mycobacterium sp. strain PYR-1 This study
 pBAD/Thio-TOPO vector Ampr pMB1 origin, six-His-Thioredoxin open reading frame, arabinose induced Invitrogen
katG-pBAD/Thio plasmid pBAD/ThioFusion with the katG gene of Mycobacterium strain PYR-1 This study