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- W2804136211 abstract "Phenoxazine and quinone are typical electron mediators in natural and engineered systems. Although the electron shuttling process of quinone has been well studied, phenoxazine is poorly characterized. Here, a model phenoxazine (resazurin) was examined as an electron mediator in a bioelectrochemical system with Shewanella oneidensis MR-1. Results showed that the current generation was substantially enhanced by the presence of phenoxazine, and was almost unaffected even after replacing the original medium with a fresh medium without phenoxazine. This is completely different to the well-known quinones used as electron mediators. Further study suggested that, resorufin (RR), as an intermediate product, was deposited in situ onto the electrode. The RR deposition was suggested to be a dominant mechanism for stabilizing the electron shuttling efficiency by phenoxazine. This study proposed a novel electron shuttling mechanism of phenoxazine and may provide a new insight into the extracellular electron transfer." @default.
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- W2804136211 date "2018-06-06" @default.
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- W2804136211 title "Sustainable Electron Shuttling Processes Mediated by <i>In Situ-</i> Deposited Phenoxazine" @default.
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- W2804136211 doi "https://doi.org/10.1002/celc.201800470" @default.
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