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. 2003 Jan;185(2):453–460. doi: 10.1128/JB.185.2.453-460.2003

TABLE 3.

Phenotypic characterization of aba mutants in P. fluorescens

Strain or aba mutant adnA Swimming Biofilm Sand column adhesion assaya Chemotaxisb Flagellac Fold increase effect of AdnA on gene expressiond
Pf0-1 + + + 99 ± 1 + (33) + ND
Pf0-2x 65 ± 20 ND
Pf0-2x (adnA) + + + 92 ± 0.7 + (28) + ND
aba18 + 80 ± 15
+ + + 97 ± 1 + (10) + 6
aba51 + 64 ± 6
+ + + 94 ± 2 + (12) + 8
aba120 47 ± 23
+ + 63 ± 20 64
aba160 + 27 ± 8
+ + 58 ± 2 56
aba175 62 ± 8
+ + 76 ± 6 34 (11)
aba177 26 ± 12
+ + 80 ± 14 25
aba203 + 38 ± 24
+ + + 88 ± 8 + (16) + 35 (7.8)
a

Values are mean percentages of cells that attached ± standard errors.

b

For strains exhibiting chemotaxis, the distance moved (in millimeters) is shown in parentheses.

c

Confirmed by electron microscopy.

d

Fold increase due to AdnA was estimated by β-galactosidase assays. All assays included the control consisting of aba strains harboring pPC101, which carries a deletion of the N-terminus domain of AdnA. Values shown are those obtained with adnA expressed from plasmid pPC100, apart from those in parentheses, which were determined from strains in which adnA::Sm/Sp was replaced by wild-type adnA (see Materials and Methods for details). LacZ activity for all insertion mutants was 2 to 7 Miller units, except for the aba175 mutant, which was 17 to 18 Miller units. ND, not determined.