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. Author manuscript; available in PMC: 2010 Aug 1.
Published in final edited form as: Mol Microbiol. 2009 Jul 6;73(3):341–351. doi: 10.1111/j.1365-2958.2009.06755.x

Table 2.

Mutations in the TraR N Terminal Domain that are defective in transcriptiona

Mutation traI Promoter Activity at the Indicated OOHL Concentrations
0.1 nM 1 nM 10 nM 100 nM
Wild type (100)b (100)b (100)b (100)b
Vector Control <1 <1 <1 <1
D6E 20 15 28 42
D6G <1 <1 <1 <1
K7R 9 31 28 44
D10N <1 <1 <1 <1
A13L <1 1 20 7
E15K 6 18 31 46
D17E 12 11 34 21
I20W 5 12 38 14
H44K 5 18 34 42
P71H <1 <1 <1 8
K74E <1 6 16 8
R75E 8 32 41 48
R77E <1 <1 2 1
S78E 12 26 22 28
R79E 32 48 36 36
K80E 3 19 24 23
N122A <1 3 22 29
N122D <1 1 10 16
G123R <1 <1 <1 <1
D144R <1 <1 5 23
a

All mutations included in this list functioned at levels 50% or lower than wild type TraR in the presence of 100 nM OOHL. Data are presented as a percentage of wild type.

b

Wild type TraR expressed the promoter, a traI-lacZ fusion, at 700, 1500, 2600 and 3000 units of ∃-galactosidase activity at 0.1 nM, 1 nM, 10 nM and 100 nM of OOHL, respectively.