TY - JOUR
T1 - Towards patterned bioelectronics
T2 - facilitated immobilization of exoelectrogenic Escherichia coli with heterologous pili
AU - Lienemann, Michael
AU - TerAvest, Michaela A.
AU - Pitkänen, Juha Pekka
AU - Stuns, Ingmar
AU - Penttilä, Merja
AU - Ajo-Franklin, Caroline M.
AU - Jäntti, Jussi
N1 - Funding Information:
Received 20 March, 2018; revised 2 July, 2018; accepted 7 August, 2018. *For correspondence. E-mail michael.lienemann@vtt.fi; Tel. +358 20 722 7153; Fax +358 20 722 7001. †Denotes equal contribution. Microbial Biotechnology (2018) 11(6), 1184–1194 doi:10.1111/1751-7915.13309 Funding Information This research has been financially supported through the VTT Frontier Programme, the Biosolar programme granted by Tekes – the Finnish Funding Agency for Innovation (Diary No. 2299/31/2012; Decision No. 40044/13) and the Academy of Finland through a postdoctoral research grant (Decision No. 277121 to ML) and research grants SYNECO2 (Decision No. 272569 to JJ) and OPTOBIO (Decision No. 287011 to MP). Work at the Molecular Foundry was supported by the Office of Science, Basic Energy Sciences programme of the U.S. Department of Energy (Contract No. DE-AC02-05CH11231). CMAF and MAT acknowledge support from Office of Naval Research (Award number N000141310551).
Funding Information:
Funding Information This research has been financially supported through the VTT Frontier Programme, the Biosolar programme granted by Tekes ? the Finnish Funding Agency for Innovation (Diary No. 2299/31/2012; Decision No. 40044/13) and the Academy of Finland through a postdoctoral research grant (Decision No. 277121 to ML) and research grants SYNECO2 (Decision No. 272569 to JJ) and OPTOBIO (Decision No. 287011 to MP). Work at the Molecular Foundry was supported by the Office of Science, Basic Energy Sciences programme of the U.S. Department of Energy (Contract No. DE-AC02-05CH11231). CMAF and MAT acknowledge support from Office of Naval Research (Award number N000141310551). This research has been financially supported through the VTT Frontier Programme, the Biosolar programme granted by Tekes ? the Finnish Funding Agency for Innovation (Diary No. 2299/31/2012; Decision No. 40044/13) and the Academy of Finland through a postdoctoral research grant (Decision No. 277121 to ML) and research grants SYNECO2 (Decision No. 272569 to JJ) and OPTOBIO (Decision No. 287011 to MP). Work at the Molecular Foundry was supported by the Office of Science, Basic Energy Sciences programme of the U.S. Department of Energy (Contract No. DE-AC02-05CH11231). CMAF and MAT acknowledge support from Office of Naval Research (Award number N000141310551). Dr. Heather M. Jensen, Matt Hepler, Cheryl P. Goldbeck and Dr. Behzad Rad are thanked for supporting this research at the LBNL through advice and practical help. The authors would like to thank Prof. Paul Orndorff at North Carolina State University for generously providing the pSH2 plasmid, and Prof. David Thanassi as well as Nadine Henderson at Stony Brook University for their generous gift of Fim pili specific antibodies. We are grateful to Dr. J?rg Deutzmann for a critical review of the manuscript.
Funding Information:
This research has been financially supported through the VTT Frontier Programme, the Biosolar programme granted by Tekes – the Finnish Funding Agency for Innovation (Diary No. 2299/31/2012; Decision No. 40044/13) and the Academy of Finland through a postdoctoral research grant (Decision No. 277121 to ML) and research grants SYNECO2 (Decision No. 272569 to JJ) and OPTOBIO (Decision No. 287011 to MP). Work at the Molecular Foundry was supported by the Office of Science, Basic Energy Sciences programme of the U.S. Department of Energy (Contract No. DE-AC02-05CH11231). CMAF and MAT acknowledge support from Office of Naval Research (Award number N000141310551). Dr. Heather M. Jensen, Matt Hepler, Cheryl P. Goldbeck and Dr. Behzad Rad are thanked for supporting this research at the LBNL through advice and practical help. The authors would like to thank Prof. Paul Orndorff at North Carolina State University for generously providing the pSH2 plasmid, and Prof. David Tha-nassi as well as Nadine Henderson at Stony Brook University for their generous gift of Fim pili specific antibodies. We are grateful to Dr. Jo€rg Deutzmann for a critical review of the manuscript.
Publisher Copyright:
© 2018 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology.
Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.
PY - 2018/11/1
Y1 - 2018/11/1
N2 - Biosensors detect signals using biological sensing components such as redox enzymes and biological cells. Although cellular versatility can be beneficial for different applications, limited stability and efficiency in signal transduction at electrode surfaces represent a challenge. Recent studies have shown that the Mtr electron conduit from Shewanella oneidensis MR-1 can be produced in Escherichia coli to generate an exoelectrogenic model system with well-characterized genetic tools. However, means to specifically immobilize this organism at solid substrates as electroactive biofilms have not been tested previously. Here, we show that mannose-binding Fim pili can be produced in exoelectrogenic E. coli and can be used to selectively attach cells to a mannose-coated material. Importantly, cells expressing fim genes retained current production by the heterologous Mtr electron conduit. Our results demonstrate the versatility of the exoelectrogenic E. coli system and motivate future work that aims to produce patterned biofilms for bioelectronic devices that can respond to various biochemical signals.
AB - Biosensors detect signals using biological sensing components such as redox enzymes and biological cells. Although cellular versatility can be beneficial for different applications, limited stability and efficiency in signal transduction at electrode surfaces represent a challenge. Recent studies have shown that the Mtr electron conduit from Shewanella oneidensis MR-1 can be produced in Escherichia coli to generate an exoelectrogenic model system with well-characterized genetic tools. However, means to specifically immobilize this organism at solid substrates as electroactive biofilms have not been tested previously. Here, we show that mannose-binding Fim pili can be produced in exoelectrogenic E. coli and can be used to selectively attach cells to a mannose-coated material. Importantly, cells expressing fim genes retained current production by the heterologous Mtr electron conduit. Our results demonstrate the versatility of the exoelectrogenic E. coli system and motivate future work that aims to produce patterned biofilms for bioelectronic devices that can respond to various biochemical signals.
KW - OtaNano
UR - http://www.scopus.com/inward/record.url?scp=85053461129&partnerID=8YFLogxK
U2 - 10.1111/1751-7915.13309
DO - 10.1111/1751-7915.13309
M3 - Article
AN - SCOPUS:85053461129
SN - 1751-7915
VL - 11
SP - 1184
EP - 1194
JO - Microbial Biotechnology
JF - Microbial Biotechnology
IS - 6
ER -