EC Number   |
Substrates |
Organism |
Products |
Reversibility |
|---|
   1.20.2.1 | arsenite + H2O + 2,6-dichlorophenolindophenol |
- |
arsenite-oxidising bacterium NT-26 |
arsenate + reduced 2,6-dichlorophenolindophenol |
- |
? |
| 1.20.2.1 | more |
mediated electrocatalytic voltammetry study. In the absence of arsenite, or the enzyme, cytochrome c552 cofactor exhibits a well-defined single electron reversible response at a Au electrode modified with the long chain mercaptoundecanoic acid, which presents a self-assembled monolayer of negatively charged functional groups to the protein surface. In the presence of arsenite and enzyme a variety of CV waveforms are observed depending on sweep rate and substrate concentration. Arsenite binding is very fast |
Rhizobium sp. |
? |
- |
? |
| 1.20.2.1 | more |
mediated electrocatalytic voltammetry study. In the absence of arsenite, or the enzyme, cytochrome c552 cofactor exhibits a well-defined single electron reversible response at a Au electrode modified with the long chain mercaptoundecanoic acid, which presents a self-assembled monolayer of negatively charged functional groups to the protein surface. In the presence of arsenite and enzyme a variety of CV waveforms are observed depending on sweep rate and substrate concentration. Arsenite binding is very fast |
Rhizobium sp. NT-26 |
? |
- |
? |
