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Other cellular peroxiredoxins can be inhibited in the presence of high concentrations of H2O2 by the over oxidation of the peroxidatic cysteine residue to form sulphinic or sulphonic derivatives (Woo et al, 2003).
Variation in the total oxide intensity (Iox) for all the six temperatures over oxidation time up to 60 min is shown in Figure 3.
The current production systems suffer from either low conversion or over oxidation.
No over oxidation occurred and no CO or CO2 was observed by GC/TCD.
No over oxidation occurred and no CO or CO2 was observed during the reaction.
Previous research [3] indicates that grain sizes can exert significant control over oxidation and dissolution rates.
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Catalysts based on vanadium oxides are quite active and can cause over-oxidation to maleic anhydride or carbon oxides.
It is suggested that the recovery of the over-oxidized Alr4641 is facilitated by the sulfiredoxin (Srx) protein, which reverses the over-oxidation in vivo [ 40].
All evidences point to the advantageous use of lower oxidative temperatures: more effective penetration of stabilization depth, lessen destructive effects of over-oxidation, and potentially shorter processing times.
XPS measurements suggested that over-oxidation of Pt was concomitant with this TOR decrease.
A major cause of catalyst deactivation is over-oxidation under oxygen rich conditions.
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