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. 2012 Sep 18;7(9):e44673. doi: 10.1371/journal.pone.0044673

Table 2. Selected Bacterial Strains and Plasmids Used in This Study.

Strain/Plasmid Description Referenceb
Db10 Serratia marcescens Wild type [25]
NRS2992 Db10 SMA2290::Tn5 This study
SAN2 Db10 (Δalb1) in-frame This study
SAN3 Db10 (Δalb2) in-frame This study
SAN4 Db10 (Δalb3) in-frame This study
SAN88 Db10 (Δalb351–262) in-frame This study
SAN5 Db10 (Δalb4–5) in-frame This study
SAN60 Db10 (Δalb6) in-frame This study
SAN96 Db10 (ΔSMA4147) in-frame This study
SAN112 Db10 (ΔSMA2452::Cml) This study
SAN100 Db10 PT5-alb1–6 (T5 promoter replacing native promoter upstream of alb1) This study
ATCC274 Serratia marcescens Wild type A.T.C.C.
Plasmids
pSUPROM Vector for constitutive expression of cloned genes under the control of the E. coli Tat promoter (KanR) [44]
pSAN1 alb1 coding sequence in pSUPROM This study
pSAN2 alb2 coding sequence in pSUPROM This study
pSAN3 alb3 coding sequence in pSUPROM This study
pSAN38 alb6 coding sequence in pSUPROM This study
pSAN46 SMA2452 coding sequence in pSUPROM This study