TY - JOUR
T1 - PEDOT:PSS-based Multilayer Bacterial-Composite Films for Bioelectronics
AU - Zajdel, Tom J.
AU - Baruch, Moshe
AU - Méhes, Gábor
AU - Stavrinidou, Eleni
AU - Berggren, Magnus
AU - Maharbiz, Michel M.
AU - Simon, Daniel T.
AU - Ajo-Franklin, Caroline M.
N1 - Funding Information:
Work at the Molecular Foundry was supported by the Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231. TJZ was supported by the National Science Foundation Graduate Research Fellowship under Grant No. DGE 1106400. MBaruch and CAF were supported by Office of Naval Research, Award number N000141310551. GM, MBerggren, and DTS were funded by: the Knut and Alice Wallenberg Foundation (project “Tail of the Sun”). MBerggren and DS were additionally supported by the Swedish Foundation for Strategic Research. GM was also supported with a grant from the Swedish MSCA Seal of Excellence program. ES was funded by a Marie Sklodowska Curie Individual Fellowship (MSCA-IF-EF-ST, Trans-Plant, 702641). MMM is a Chan Zuckerberg Biohub investigator. We thank Michael Connolly for his assistance in 3D-printing the electrode mount, Travis Massey and Burak Ozdul for their assistance in SEM sample preparation, Lin Su for his assistance with S. oneidensis native biofilm culture, and Kosala Wijeratne, Mikhail Vagin, and Valerio Beni for their advice on EIS. The Δbfe and ΔmtrB strains were a generous gift from Jeffrey Gralnick.
Publisher Copyright:
© 2018, The Author(s).
PY - 2018/12/1
Y1 - 2018/12/1
N2 - Microbial electrochemical systems provide an environmentally-friendly means of energy conversion between chemical and electrical forms, with applications in wastewater treatment, bioelectronics, and biosensing. However, a major challenge to further development, miniaturization, and deployment of bioelectronics and biosensors is the limited thickness of biofilms, necessitating large anodes to achieve sufficient signal-to-noise ratios. Here we demonstrate a method for embedding an electroactive bacterium, Shewanella oneidensis MR-1, inside a conductive three-dimensional poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) matrix electropolymerized on a carbon felt substrate, which we call a multilayer conductive bacterial-composite film (MCBF). By mixing the bacteria with the PEDOT:PSS precursor in a flow-through method, we maintain over 90% viability of S. oneidensis during encapsulation. Microscopic analysis of the MCBFs reveal a tightly interleaved structure of bacteria and conductive PEDOT:PSS up to 80 µm thick. Electrochemical experiments indicate S. oneidensis in MCBFs can perform both direct and riboflavin-mediated electron transfer to PEDOT:PSS. When used in bioelectrochemical reactors, the MCBFs produce 20 times more steady-state current than native biofilms grown on unmodified carbon felt. This versatile approach to control the thickness of bacterial composite films and increase their current output has immediate applications in microbial electrochemical systems, including field-deployable environmental sensing and direct integration of microorganisms into miniaturized organic electronics.
AB - Microbial electrochemical systems provide an environmentally-friendly means of energy conversion between chemical and electrical forms, with applications in wastewater treatment, bioelectronics, and biosensing. However, a major challenge to further development, miniaturization, and deployment of bioelectronics and biosensors is the limited thickness of biofilms, necessitating large anodes to achieve sufficient signal-to-noise ratios. Here we demonstrate a method for embedding an electroactive bacterium, Shewanella oneidensis MR-1, inside a conductive three-dimensional poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) matrix electropolymerized on a carbon felt substrate, which we call a multilayer conductive bacterial-composite film (MCBF). By mixing the bacteria with the PEDOT:PSS precursor in a flow-through method, we maintain over 90% viability of S. oneidensis during encapsulation. Microscopic analysis of the MCBFs reveal a tightly interleaved structure of bacteria and conductive PEDOT:PSS up to 80 µm thick. Electrochemical experiments indicate S. oneidensis in MCBFs can perform both direct and riboflavin-mediated electron transfer to PEDOT:PSS. When used in bioelectrochemical reactors, the MCBFs produce 20 times more steady-state current than native biofilms grown on unmodified carbon felt. This versatile approach to control the thickness of bacterial composite films and increase their current output has immediate applications in microbial electrochemical systems, including field-deployable environmental sensing and direct integration of microorganisms into miniaturized organic electronics.
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U2 - 10.1038/s41598-018-33521-9
DO - 10.1038/s41598-018-33521-9
M3 - Article
C2 - 30327574
AN - SCOPUS:85055072205
SN - 2045-2322
VL - 8
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 15293
ER -