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. 2004 Nov;186(21):7149–7160. doi: 10.1128/JB.186.21.7149-7160.2004

TABLE 3.

Summary of constitutive mutants

Functional group Straina No. of insertionsb Assay resultsc
Functional or putative functiond Functional reference Constitutive reference
I II
Replication, recombination, and repair dam mutant 3 DNA adenine methylase 61 83, 84, 89
dnaQ mutant 2 Epsilon subunit of DNA polymerase III (3′-5′ exonuclease) 50 89, 100
polA mutant 1 DNA polymerase I 50 5, 89
recG mutant 4 Branch-specific helicase or fork reversal 67 2, 56
recN mutant 1 Recombination and repair gene 85 14, 27, 99
rep mutant 7 Helicase 58 81, 105
ruvA mutant 3 Holiday junction helicase (branch migration) 108 2
ruvB mutant 2 Holiday junction helicase (branch migration) 108 2e
ruvC mutant 2 Holiday junction endonuclease 108 2, 55
uvrD mutant 2 DNA-dependent helicase II 32 6, 81, 89
Chromosome dimer resolution ftsK mutant 14 Cell division protein or SpoIIIa-like function 24, 28 54
xerC mutant 8 Site-specific recombinase 44 40
xerD mutant 7 Site-specific recombinase 44 40
yncD yddW mutantf 1 Putative outer membrane receptor for iron transport or putative lipoprotein 9 This work
Transcription and transcription regulation lexA mutant 2 Global regulator (repressor) for SOS regulon 32 73
rpoZ mutant 1 RNA-polymerase subunit omega (polar on recG?) 12 This work
spoT mutant 6 ppGpp synthetase (polar on recG?) 12 This work
Nucleoside metabolism dcd mutant 1 2′-Deoxycytosine deaminase 75 This work
folA mutant 1 Dihydrofolate reductase 36 This work
folK mutant 2 6-Hydroxymethyl-7,8-dihydropterin pyrophosphokinase 36 This work
purA mutant 1 Adenylosuccinate synthase 110 This work
purE mutant 1 Phosphoribosylaminoimidazole carboxylase 110 This work
purF mutant 2 Glutamine phosphoribosylpyrophosphate amidotransferase 110 This work
purL mutant 1 Phosphoribosylformylglycinamide synthase 110 This work
thyA mutant 1 Thymidylate synthase 75 1g
Membrane structure/function acrB mutant 14 Drug efflux pump 76 This work
cvpA mutant 1 Colicin V production protein (polar on purF?) 29, 30 This work
dsbB mutant 1 Disulfide oxidoreductase 46 This work
ompA mutant 1 Outer membrane protein A 76 This work
tolC mutant 9 Channel-tunnel spanning the outer membrane and periplasm 76 This work
Miscellaneous arpB mutant 1 Putative regulatory protein with ankyrin repeats 9 This work
damX mutant 4 Overproduction interferes with cell division (polar on dam?) 57, 59 This work
ftsE mutant 1 ABC transporter? Salt transport? 22, 34 This work
ftsX mutant 3 ABC transporter? Salt transport? 22, 34 This work
rluD ecfD mutanth 1 Pseudouridylate synthase; null mutants grow poorly or putative lipoprotein regulated by sigma E 9, 21, 79, 87 This work
This work
tdcE mutant 2 Threonine dehydratase 41 This work
tynA mutant 1 Tyramine oxidase 74 This work
yebC mutant 1 Putative membrane protein (polar on ruvC?) 4, 9 This work
yehB mutant 1 Putative outer membrane export usher protein 9 This work
yejM mutant 1 Putative sulfatase 9 This work
yfgM mutant 1 Putative N-terminal transmembrane domain 9 This work
yhcB mutant 1 Conserved bacterial protein of unknown function 9 This work
a

Alternate gene names: arpB, b1720/b1721; ecfD, b2595; envC, yibP; rluD, sfhB; yfgL, b2512; yfgM, b2513; yncD, b1451; yddW, b1491.

b

Number of independent insertions isolated in each gene. Single hits were confirmed by P1 transduction.

c

Performance of transposon insertion mutant strains in quantitative assays. I, β-galactosidase assay; II, RecA Western blot assay. Open circles indicate those strains whose assay results exceeded that of the wild type by more than 1 standard deviation; closed circles indicate those strains whose assay results were at least twice as high as wild-type levels.

d

Functions according to the NCBI website (http://www.ncbi.gov).

e

Although ruvB mutants were not directly assayed in the cited study, we assume they are SOS constitutive since RuvAB acts as a complex.

f

This insertion mutant has two transposons (see text).

g

thyA mutants have never been assayed for the SOS constitutive phenotype; however, this review suggests that they are SOS constitutive based on their phenotypes.

h

The transposon insertion in this strain is located between the two genes.