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. 2003 Aug;185(16):4956–4972. doi: 10.1128/JB.185.16.4956-4972.2003

TABLE 5.

Summary of PM data for two-component mutantsa

System (HK/RR) Function(s) No. of phenotypesb
New phenotype(s) or function(s)
Gained Lost
ArcA (RR) Respiration control 2 47 Nonec
ArcB (hybrid) Respiration control 2 59 Nonec
AtoS/AtoC Acetoacetate metabolism 1 5 Glucuronamide use and NaCl sensitivity
BaeS/BaeR Unknown 0 4 Sodium tungstate sensitivity
BarA (hybrid) Hydrogen peroxide sensitivity 2 0 Melibiose metabolism
UvrY (RR) Hydrogen peroxide sensitivity 2 5 Melibiose metabolism
CpxA/CpxR Cell envelope stress 0 23 Ethylene glycol sensitivity
CusS/CusR Response to copper 0 1 1,10-Phenanthroline sensitivity
DcuS/DcuR C4 dicarboxylate utilization 0 9 None
EnvZ/OmpR Osmotic regulation 12 8 Increased use of carbohydrates, cephalosporin resistance
KdpD/KdpE Potassium transport 1 1 Novobiocin resistance
NarP (RR) Nitrate regulation 0 1 Chelator sensitivity
NtrB/NtrC Nitrogen regulation 2 23 Aminoglycoside sensitivity
PhoQ/PhoP Response to magnesium 2 0 Increased use of fructose and mannitol
PhoR/PhoB Phosphate regulation 0 8 Noned
QseC/QseB Quorum sensing 0 5 Metal sensitivity
RcsB (RR) Capsule synthesis 0 6 NaCl and trimethoprim sensitivity
RcsC/YojN(Hpt)/RcsB Capsule synthesis 0 6 NaCl and trimethoprim sensitivity
YojN(Hpt) 0 6 NaCl sensitivity
RssB (RR) σS Stability 0 53 Decreased use of C4 di- and monocarboxylates and amino acid N sources
RstB/RstA Unknown 0 3 Ketoprofen, pridinol, and troleandomycin sensitivity
UhpB/UhpA Hexose phosphate uptake 0 2 None
a

The following 15 other two-component mutants did not have altered phenotypes: BasS/BasR, CheA (HK)/CheB (RR)/CheY (RR), DpiB/DpiA, CreC/CreB, EvgS/EvgA, FimZ (RR), ZraS/ZraR, NarX/NarL, NarQ (HK), TorS/TorR, YedV/YedW, YehU/YehT, YfhK (HK), YfhA (RR), and YpdA/YpdB.

b

Phenotypes gained means PM assays showing increased growth or respiration (positive values in Table 4). Phenotypes lost means PM assays showing decreased growth or respiration (negative values in Table 4).

c

The arcA and arcB mutants had many phenotypes that were attributed to membrane-associated functions, which may be considered new.

d

As mentioned in the text, two of the three phoBR mutants showed increased sensitivity to aminoglycoside.