Skip to main content
. 2016 Jul 17;197(16):2653–2663. doi: 10.1128/JB.00332-15

TABLE 3.

Predicted and verified RcGTA recipient capability genese

R. capsulatus genee Annotation Predicted/verified function(s) and/or characteristic(s) of gene product WT/ΔctrA ratio
Predicted TMS (n) Phenotype of mutant(s)
Stationarya Logb Transformationc RcGTA recipient capabilityd
rcc00197 comF Unknown; required for DNA transport from periplasm to cytoplasm 3.23 5.35 1 Not detectable Unknown
rcc00460 comM Unknown; putative ATPase and helicase-like domains 2.91 1.89 0 Variable; 0– to 300-fold reduction Unknown
rcc02362 comEC-rec2 Integral membrane protein; transports DNA from periplasm to cytoplasm 4.88 2.67 6 Not detectable Unknown
rcc03098 dprA Recombination mediator; loads RecA into ssDNA 9.38 3.75 0 Not detectable Not detectable
rcc01751 recA Recombination protein A; RecA; DNA repair and homologous recombination 1.47 1.22 0 Not detectable Not detectable
rcc01663 ctrA Cell cycle transcriptional regulator CtrA; regulates transcription of RcGTA and com genes 0.94 1.04 0 Unknown Not detectable
a

Ratio of WT to ΔctrA microarray expression values for cells grown to the exponential phase of growth.

b

Ratio of WT to ΔctrA microarray gene expression values for cells grown to the stationary phase of growth.

c

A 107-fold reduction in transformation was used as the limit of detection in other species.

d

A 106-fold reduction in recipient capability was used as the limit of detection in R. capsulatus.

e

Shown are predicted and verified RcGTA recipient capability genes, their annotations, predicted or verified functions, expression levels in the ΔctrA mutant versus the wild type in both stationary and log phases, the numbers of predicted transmembrane segments (TMS), the phenotypes in natural transformation systems, and the phenotypes resulting from mutations in these genes in natural transformation systems and in RcGTA recipient capability. Microarray expression values are derived from data reported in reference 61, and ΔdprA, ΔrecA, and ΔctrA mutant phenotypes were reported previously by Brimacombe et al. (13).