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. Author manuscript; available in PMC: 2013 Dec 17.
Published in final edited form as: Adv Microbiol. 2012 Dec 1;2(4):10.4236/aim.2012.24065. doi: 10.4236/aim.2012.24065

Table 1.

Strains and plasmids used in this study.

Strain or plasmid Description Reference or source
S. cerevisiae
InvSc1 Diploid uracil auxotroph Invitrogen
Bacterial strains
S17-1 λpir Escherichia coli strain used for conjugation [22]
EC100D E. coli strain used for cloning, pir-116 Epicentre
ER2566 E. coli strain used for protein expression New England Biolabs
CMS376 wild-type Serratia marcescens, PIC strain number 3611 Presque Isle Cultures
CMS1779 hexS::pStvz3 in WT (CMS376), hexS-1 This study
CMS2210 ΔhexS, (hexS-Δ1 allele) in CMS376 This study
CMS3125 CMS2210 + pMQ294 hexS complementation strain This study
CMS3142 nuoC::pStvZ3 in CMS376 This study
CMS1317 alaT::pMQ118 in CMS376 This study
Plasmids
pMal-C2 Maltose binding protein fusion construct New England Biolabs
pStvZ3 oriR6K lacZ nptII promoter probe [20]
pMQ118 suicide vector nptII, rpsL, oriT, URA3, CEN6/ARSH4 [19]
pMQ197 pMQ118 with internal fragment of alaT This study
pMQ236 allelic replacement vector, pMQ118 with I-SceI site [19]
pMQ240 I-SceI-expression plasmid, aacC1, oripSC101ts [19]
pMQ268 pStvZ3 + pigA internal fragment [20]
pMQ294 pMQ236 with hexS open reading frame This study
pMQ296 pMQ294 with hexS-Δ1 mutant allele This study
pMQ342 pStvZ3 with internal fragment of nuoC This study
pMQ402 pMAL-C2 + hexS (MBP-HexS fusion construct) This study