Type
ArticleAuthors
Zhu, XiupingYates, Matthew D.
Hatzell, Marta C.
Rao, Hari Ananda

Saikaly, Pascal

Logan, Bruce E.
KAUST Department
Water Desalination and Reuse Research Center (WDRC)Biological and Environmental Sciences and Engineering (BESE) Division
Environmental Science and Engineering Program
Environmental Biotechnology Research Group
KAUST Grant Number
KUS-I1-003-13Date
2014-01-02Online Publication Date
2014-01-02Print Publication Date
2014-01-21Permanent link to this record
http://hdl.handle.net/10754/563345
Metadata
Show full item recordAbstract
There is great controversy on how different set anode potentials affect the performance of a bioelectrochemical system (BES). It is often reported that more positive potentials improve acclimation and performance of exoelectrogenic biofilms, and alter microbial community structure, while in other studies relatively more negative potentials were needed to achieve higher current densities. To address this issue, the biomass, electroactivity, and community structure of anodic biofilms were examined over a wide range of set anode potentials (-0.25, -0.09, 0.21, 0.51, and 0.81 V vs a standard hydrogen electrode, SHE) in single-chamber microbial electrolysis cells. Maximum currents produced using a wastewater inoculum increased with anode potentials in the range of -0.25 to 0.21 V, but decreased at 0.51 and 0.81 V. The maximum currents were positively correlated with increasing biofilm biomass. Pyrosequencing indicated biofilm communities were all similar and dominated by bacteria most similar to Geobacter sulfurreducens. Differences in anode performance with various set potentials suggest that the exoelectrogenic communities self-regulate their exocellular electron transfer pathways to adapt to different anode potentials. © 2013 American Chemical Society.Citation
Zhu, X., Yates, M. D., Hatzell, M. C., Ananda Rao, H., Saikaly, P. E., & Logan, B. E. (2014). Microbial Community Composition Is Unaffected by Anode Potential. Environmental Science & Technology, 48(2), 1352–1358. doi:10.1021/es404690qSponsors
This research was supported by Award KUS-I1-003-13 from the King Abdullah University of Science and Technology (KAUST). The authors also want to thank the three anonymous reviewers for their constructive comments on the original manuscript.Publisher
American Chemical Society (ACS)PubMed ID
24364567ae974a485f413a2113503eed53cd6c53
10.1021/es404690q
Scopus Count
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