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. 2022 Dec 6;13(6):e02422-22. doi: 10.1128/mbio.02422-22

TABLE 5.

Bacterial strains and plasmids used in this study

Strain or plasmid Descriptiona Source
Bacterial strains
 JDW4203 X. campestris pv. campestris wild-type isolate 8004, Rifr 52
 JDW4204 X. campestris pv. campestris 8004 Δsah, Rifr This study
 JDW4205 X. campestris pv. campestris 8004 Δsah pLAFR3-sah, Rifr Tcr This study
 JDW4209 E. coli BL21(DE3) harboring pLIC-sah plasmid, Ampr This study
 JDW3005 P. aeruginosa PA01 Lab collection
 JDW4208 Pseudomonas sp. ADAK18 45
Plasmids
 p2P24Km Suicide vector for in-frame deletion, derived from pEx18-KCL containing SacB selectable marker, Kmr 53
 p2P24Km-sah p2P24Km containing SAH fragment, Kmr This study
 pRK600 Helper plasmid for triparental mating ColE1 oriV tra+ RP4 oriT, Cmr 54
 pLAFR3 X. campestris pv. campestris expression vector containing RK2 replicon, TcR 56
 pLAFR3-sah Complementation vector, pLAFR3 containing sah gene, Tcr This study
 pLICtrPC-HA Protein expression vector, Ampr Lab stock
 pLIC-sah Protein expression vector, pLICtrPC-HA containing XccSAH gene, Ampr This study
 pLIC-Mesh1 Protein expression vector, pLICtrPC-HA containing C. elegans Mesh1 gene, Ampr This study
a

Rifr, Kmr, Cmr, Tcr and Ampr indicate resistance to rifampicin, kanamycin, chloramphenicol, tetracycline and ampicillin, respectively.