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. 2003 Oct;69(10):5957–5967. doi: 10.1128/AEM.69.10.5957-5967.2003

TABLE 1.

Description of strains and plasmids used in this study

Strains and plasmids Description Reference or source
Strains
    E. coli KO11 Δfrd, CmR, carrying the Zymomonas mobilis pdc adhB cassette 38
    E. coli TOP10F′ lacIqlacZΔM15 Invitrogen
    K. oxytoca M5A1 Wild type 37
Plasmids
    pCR2.1-TOPO 3.9 Kbp, KmR AmpR, pUC origin, TA cloning vector Invitrogen
    pNEB193 AmpR cloning vector similar to pUC19 New England Biolabs
    pLOI3701 pUC18 derivative with ∼7-kbp DNA fragment, xynTxynB This study
    pLOI3702 pUC18 derivative with ∼6.3-kbp DNA fragment, xynTxynB This study
    pLOI3703 pUC18 derivative with ∼5.6-kbp DNA fragment, xynTxynB This study
    pLOI3704 pCR2.1-TOPO derivative with ∼6.0-kbp DNA fragment, xynTxynB This study
    pLOI3705 pCR2.1-TOPO derivative with ∼6.0-kbp DNA fragment, xynTB operon This study
    pLOI3706 derivative of pLOI3705 with all Klebsiella DNA removed between the two vector EcoRI sites This study
    pLOI3707 pNEB193 derivative carrying the 3.6-kbp AseI-PstI fragment with the complete xynTB coding regions (lacking regulatory sites); transcribed opposite to the lac promoter This study
    pLOI3708 pNEB193 derivative containing the 3.6-kbp AseI-PstI fragment with the complete xynTB coding regions (lacking regulatory sites); transcribed in the same direction as the lac promoter This study
    pLOI3709 Derivative of pLOI3708, ΔxynT, xynB (918-bp ClaI internal deletion of xynT) This study