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. 2004 Jun;3(3):632–645. doi: 10.1128/EC.3.3.632-645.2004

TABLE 2.

Plasmids used for this study

Plasmid Description Source or reference
pBluescript KS(−) Cloning vector Invitrogen (NV Leek, The Netherlands)
pCR2.1-TOPO TA cloning vector for cloning of PCR fragments Invitrogen (NV Leek, The Netherlands)
pCMB17apx alcAp::GFP pyr4; used for N-terminal fusion of GFP to proteins of interest V. Efimov (Piscataway, N.J.)
pDC1 A. nidulans argB gene in pIC20R 2
pHW-arg KpnI-XhoI-released argB from pDC1 inserted into pBluescript KS(−) 44
pRG1 Contains N. crassa pyr4 gene 43
pPR5 kipB containing cosmid (BamHI short fragment, 3.3 kb) from pU1 library This study
pGR1 Subclone BamHI short fragment of kipB from pPR5 into pBluescript KS(−) This study
pPR7 3.6-kb SacI-BamHI fragment of kipB cloned into pBluescript KS(−) This study
pPR11 alcAp::kipB::sgfp (kipB BamHI fragment from pPR7) cloned into pBluescript KS(−) This study
pPR13 argB gene with BamHI sites cloned into BglII sites of kipB from pPR7 (disruption construct) This study
pPR17 kipB containing cosmid (entire gene) from pU1 library This study
pPR19 4.3-kb kipB SacI subclone from pPR17 cloned into pBluescript KS(−) This study
pPR38 1.2-kb kipB fragment from ATG, PCR product with AscI and PacI sites from pPR19 inserted into pCMB17apx This study
pPND1 GFP replaced with mRFP1 (KpnI-AscI) into pPR38, alcA(p)::mRFP1::kipB, pyr4 This study