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. 2001 Sep;67(9):4305–4315. doi: 10.1128/AEM.67.9.4305-4315.2001

TABLE 3.

Complementation of P. aureofaciens 30-84 derivatives with csaR or csaR-csaI in trans

Strainf Genotype (host/plasmid) Absorbance at 367 nmac Protease activitybc Colony morphologyd Clumping phenotypee
30-84(pLAFR3) Wild type 5.91 ± 0.29 A + Semidry and rough
30-84R(pLAFR3) phzR::Tn5lacZ 0.03 ± 0.01 C + Semidry and rough
30-84R2(pZZG11) csaR::uidA-Gm/csaR+ 5.98 ± 0.39 A + Semidry and rough
30-84I/I2(pZZG11) phzI::npt csaI::uidA-Gm/csaR+ 0.04 ± 0.01 C Semidry and rough
30-84I/I2(pZZG3) phzI::npt csaI::uidA-Gm/csaR+ csaI+ 2.67 ± 0.11 B Semidry and rough
30-84I/R2(pZZG11) phzI::npt csaR::uidA-Gm/csaR+ 2.36 ± 0.20 B + Semidry and rough
30-84I2/R(pZZG3) csaI::uidA-Gm phzR:Tn5lacZ/csaR+csaI+ 2.57 ± 0.20 B + Semidry and rough
30-84R/R2(pZZG11) phzR::Tn5lacZ, csaR::uidA-Gm/csaR+ 2.42 ± 0.19 B Semidry and rough
30-84.gacA(pZZG3) gacA::npt/csaR+csaI+ 0.03 ± 0.00 C Shiny and mucoid +
a

Phenazines were extracted from supernatants of 24-h-old bacterial cultures grown in PPM-D and quantified by measuring absorbance at 367 nm. 

b

Exoprotease activity in supernatants of 24-h-old broth cultures was determined by a modified Lowry method using casein as the substrate. 

c

All values are means ± standard deviations of two experiments, with three replicates per experiment. Values followed by the same letter in a column are not significantly different (P = 0.05). 

d

Bacterial strains were cultured on KMB agar, and 2 days later the colonies were examined for roughness and mucoidy. 

e

Bacterial strains were cultured on KMB broth for 24 h, and the cultures were stained with Congo red and observed for the presence of the clumping phenotype. 

f

The presence of the vector pLAFR3 alone had no effect on any of the strains listed (data not shown).