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. Author manuscript; available in PMC: 2012 Apr 1.
Published in final edited form as: J Mol Biol. 2010 Dec 31;407(3):333–353. doi: 10.1016/j.jmb.2010.12.037

Table 2.

The effect of tri-alanine substitutions of σ70 R4 on basal transcription from the class II fumC, inaA and micF promoters.

Tri-Alanine Stretches ofσ70R4 β-galactosidase activity (% of wild type)
fumC micF inaA
P531A-D533A 134 ±6 132 ±18 124 ±4
S534A-T536A 98 ±15 88 ±10 118 ±5
T537A-S539A 81 ±13 84 ±11 137 ±8
L540A-A542A 88 ±22 125 ±9 116 ±4
A543A-H545A 116 ±18 105 ±14 98 ±4
D46A-L548A 56 ±5 100 ±7 117 ±6
A549A-L551A 174 ±18 121 ±10 92 ±4
T552A-R554A 177 ±13 107 ±4 97 ±6
E555A-K557A 10 ±12 122 ±10 110 ±3
V558A-R560A 151 ±8 108 ±8 89 ±9
M561A-F563A 59 ±5 130 ±6 120 ±6
G564A-D566A 82 ±6 130 ±4 124 ±3
M567A-T569A 72 ±10 137 ±5 73 ±8
D570A-T572A 215 ±14 183 ±13 126 ±5
L573A-E575A 90 ±17 163 ±8 104 ±5
V576A-K578A 62 ±3 209 ±24 86 ± 7
Q579A-D581A 290 ±14 208 ±8 100 ±3
V582A-R584A 64 ±7 135 ±4 108 ±6
E585A-I587A 54 ±5 156 ±7 75 ±4
R588A-I590A 219 ±18 169 ±7 78 ±3

The experiments were carried out with the same class II fusion strains and under the same conditions as those described in Table 1, except that no arabinose was added to the cultures such that SoxS expression was not induced. Expression of the fusions was determined by assay of β-galactosidase activity as described in Materials and Methods. The data are expressed as the % of the wild type value and the standard deviations are given as the % of the mean. Wild type Miller units at SoxS dependent promoters were fumC (287), inaA (77) and micF (123). As described in the text, values for mutants that are ≤ 80% of the wild type activity are taken as a meaningful difference; these values are in bold and are highlighted in grey.