The Gene and Linda Voiland School of Chemical Engineering and Bioengineering, Washington State University, Pullman, Washington 99164, United States.
Environ Sci Technol. 2011 Aug 1;45(15):6654-60. doi: 10.1021/es200865u. Epub 2011 Jun 29.
The goal of this research was to quantify the variations in redox potential and pH in Shewanella oneidensis MR-1 biofilms respiring on electrodes. We grew S. oneidensis MR-1 on a graphite electrode, which was used to accept electrons for microbial respiration. We modified well-known redox and pH microelectrodes with a built-in reference electrode so that they could operate near polarized surfaces and quantified the redox potential and pH profiles in these biofilms. In addition, we used a ferri-/ferrocyanide redox system in which electrons were only transferred by mediated electron transfer to explain the observed redox potential profiles in biofilms. We found that regardless of the polarization potential of the biofilm electrode, the redox potential decreased toward the bottom of the biofilm. In a fully redox-mediated control system (ferri-/ferrocyanide redox system), the redox potential increased toward the bottom when the electrode was the electron acceptor. The opposite behavior of redox profiles in biofilms and the redox-controlled system is explained by S. oneidensis MR-1 biofilms not being redox-controlled when they respire on electrodes. The lack of a significant variation in pH implies that there is no proton transfer limitation in S. oneidensis MR-1 biofilms and that redox potential profiles are not caused by pH.
本研究的目的是量化在电极上呼吸的希瓦氏菌(Shewanella oneidensis MR-1)生物膜中氧化还原电位和 pH 的变化。我们在石墨电极上培养了 S. oneidensis MR-1,该电极用于接受微生物呼吸的电子。我们用内置参比电极对著名的氧化还原和 pH 微电极进行了修改,以便它们可以在极化表面附近运行,并定量测量这些生物膜中的氧化还原电位和 pH 分布。此外,我们使用了一种铁氰化物/亚铁氰化物氧化还原系统,其中电子仅通过介导的电子转移进行传递,以解释生物膜中观察到的氧化还原电位分布。我们发现,无论生物膜电极的极化电位如何,氧化还原电位都朝着生物膜的底部降低。在完全氧化还原介导的控制系统(铁氰化物/亚铁氰化物氧化还原系统)中,当电极作为电子受体时,氧化还原电位朝着底部增加。生物膜和氧化还原控制体系中氧化还原分布的相反行为是由 S. oneidensis MR-1 生物膜在电极上呼吸时不受氧化还原控制解释的。pH 值没有显著变化意味着 S. oneidensis MR-1 生物膜中没有质子转移限制,并且氧化还原电位分布不是由 pH 值引起的。