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. 2001 Apr;183(8):2682–2685. doi: 10.1128/JB.183.8.2682-2685.2001

TABLE 1.

Bacterial strains and plasmids used in this study

Strain or plasmid Genotype Phenotype or characteristic Reference
A. vinelandii
 MV17 nfrX16::Tn5a Nif sup? (fast growing) 16
 MV71 glnD1::Ω glnY1 Nif GSc 5
S. meliloti
 GMI708 Strain 2011 derivative Rifr 3
 GMI3105 glnA1 GSI unadenylylatable 1
Plasmids
 pBluescriptII KS+ Ampr; cloning vector Stratagene
 pGEM-T Easy Ampr; cloning vector self-ligated at EcoRV Promega
 pHP45Ω Ampr Spr; carries Ω interposon 14
 pJRD215 IncQ broad-host-range vector; Kanr Smr 7
 pJQ200KS Gmr; sacB mobilizable cloning vector 15
 pLAFR3 IncP cosmid; Tetr 13
 pPR601 Derivative of pTA30 with HindIII fragment deleted This study
 pPR602 pBluescript KS+ with 5.2-kb PstI fragment This study
 pPR604 pBluescript KS+ with 13-kb HindIII fragment This study
 pPR608 pJRD215 with 13-kb HindIII fragment This study
 pPR611 pJRD215 with 5.2-kb ClaI/SacI fragment; glnD+ This study
 pPR612 pGEM-T Easy carrying 5.2-kb PstI fragment This study
 pPR613 pPR612 with Ω inserted at HindIII; glnD1::Ω This study
 pPR614 pJQ200KS carrying glnD1::Ω This study
 pPR615 pBluescriptII KS+ with 3.6-kb HindIII/SacI fragment This study
 pPR617 pPR615 with Ω inserted at PstI blunt end; mviN1::Ω This study
 pPR618 pJQ200KS with mviN1::Ω This study
 pTA30 Library clone with mutS glnD mviN This study
a

nfrX was the previous designation for A. vinelandii glnD (6).