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. 2018 Sep 21;17:151. doi: 10.1186/s12934-018-0991-y

Table 1.

Plasmids and strains used in this study

Plasmid or strain Relevant feature
Plasmid
 pIJ350 Versatile vector for protein expression; thiostrepton resistance marker
 pUC19 Vector for cloning genes
 pGM160 A shuttle vector containing pSG5 ori
 pK18mob Cloning vector; oriT, oriV; kanamycin resistance marker
 pXC Vector for expression of chitobiase gene (SAV_5268) under the control of xylA promoter; thiostrepton resistance marker
 pXCBR Vector for expression of chitobiase gene (SAV_5268) under the control of xylA promoter and xylR gene under the control of xylB promoter; thiostrepton resistance marker
 pLR Vector containing pSG5 ori for expression of xylR gene under the control of pld promoter; kanamycin resistance marker
 pXCPR Vector for expression of chitobiase gene (SAV_5268) under the control of xylA promoter and xylR gene under the control of pld promoter; thiostrepton resistance marker
Strain
 Escherichia coli strain JM109 recA1 endA1 gyrA96 thi-1 hsdR17 (rK− mK+) e14− (mcrA−) supE44 relA1 Δ(lacproAB)/F’[traD36 proAB + lacI q lacZΔM15]
 S. lividans 1326 WT strain
 XC Streptomyces lividans strain harboring pXC vector
 XCBR Streptomyces lividans strain harboring pXCBR vector
 XCr Streptomyces lividans strain harboring pXC and pLR vectors
 XCPR Streptomyces lividans strain harboring pXCPR vector