Abstract
A biosensor for arsenite has been developed using molybdenum-containing arsenite oxidase, prepared from the chemolithoautotroph NT-26 that oxidizes arsenite to arsenate. The enzyme was galvanostaticauy deposited for 10 min at 10 μA onto the active surface of a multiwalled carbon nanotube modified glassy carbon electrode. The resulting biosensor enabled direct electron transfer, i.e., effecting reduction and then reoxidization of the enzyme without an artificial electron-transfer mediator. Arsenite was detected within 10 s at an applied potential of 0.3 V with linearity up to 500 ppb and a detection limit of 1 ppb. The biosensor exhibited excellent reproducibility, 2% at 95% confidence interval for 12 repeated analyses of 25 ppb arsenite. Copper, a severe interfering species commonly found in groundwater, did not interfere, and the biosensor was applicable for repeated analysis of spiked arsenite in tap water, river water, and a commercial mineral water.
| Original language | English |
|---|---|
| Pages (from-to) | 7831-7837 |
| Number of pages | 7 |
| Journal | Analytical Chemistry |
| Volume | 79 |
| Issue number | 20 |
| DOIs | |
| Publication status | Published - 15 Oct 2007 |
| Externally published | Yes |
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