Table 2.
Effect of Mg2+ concentration on RNA-dependent ATPase activity of Mss116p
kobs(min−1)
|
|||
---|---|---|---|
Mg2+ (mM) | aI5γ | bI1 | poly (C) |
1 | 122 ± 18 | 64 ± 16 | 10 ± 10 |
3 | 90 ± 22 | 58 ± 12 | 60 ± 8 |
5 | 88 ± 16 | 78 ± 12 | 60 ± 12 |
8 | 112 ± 6 | 110 ± 14 | 62 ± 12 |
10 | 84 ± 18 | 80 ± 14 | 58 ± 4 |
15 | 68 ± 22 | 62 ± 18 | 36 ± 12 |
25 | 82 ± 12 | 56 ± 6 | 44 ± 12 |
35 | 34 ± 3 | 50 ± 12 | 48 ± 14 |
50 | 32 ± 4 | 28 ± 6 | 46 ± 6 |
ATPase activity was assayed with 50 nM Mss116p in reaction medium containing 100 mM KCl and different Mg2+ concentrations at 30°C, in the presence of 3 mM ATP and 300 nM intron RNAs or 0.25 μg/μl poly(C). The RNA concentrations are saturating in reaction medium containing 100 mM KCl and 8 mM Mg2+. kobs values were calculated from initial rates in time courses (see Table 1). In the absence of RNA, ATPase activity was not detectable at any of the Mg2+ concentrations (not shown). Values are the mean ± the standard deviation for triplicate assays.