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. 2008 Oct 6;8:169. doi: 10.1186/1471-2180-8-169

Table 2.

Plasmids used in this work

Plasmid Genotype or relevant features Source of reference
pBluescript SK- ColE1 ori; AmpR; cloning vector with blue-white selection Stratagene
pBAD33 p15 ori; CamR; cloning vector Beckwith Lab.
YIp5 S. cerevisiae/E. coli cloning vector. pMB1 ori; AmpR; TETR; URA3. ATCC 37061
pET101/D-TOPO ColE1 ori; AmpR; expression vector Invitrogene
pDS1B pBAD33 vector carrying the carotenogenesis genes crtE, crtB, crtI and crtY and crtX from Erwinia uredovora [40]. This work
pPR52.P.44 YIp5 bearing an insert of 12.8 kb that contains the crtR gene from base n° 88 of exon 1. This work
pCPR1.3 pBluescript SK- bearing the DNA fragment from site BamHI 4,529 to BamHI 9,895 (Figure 1). pCPR1.3 was the crtR deletion platform. This work
pcXDA.44.29 pBluescript SK- bearing the crtR gene cDNA. The cDNA measures 2,680 bp. This work
pPR32.AA.51 YIp5 bearing an insert of 4.5 kb that contains the crtR gene up to base n° 87 of exon 1. This work
pCPRB6 pBluescript SK- bearing an insert of 5.9 kb that contains the complete genomic version of crtR gene. Isolated from a SalI partial genomic library. This work
pBsiWIΔcrtR::hph pCPR1.3 BsiWI deletion and hph cassette insertion. This work
pNdecrtR::hph pCPR1.3 NdeI deletion and hph cassette insertion. This work