Abstract
Bacteria able to transfer electrons to metals are key agents in biogeochemical metal cycling, subsurface bioremediation, and corrosion processes. More recently, these bacteria have gained attention as the transfer of electrons from the cell surface to conductive materials can be used in multiple applications. In this work, we adapted electrochemical techniques to probe intact biofilms of Shewanella oneidensis MR-1 and Shewanella sp. MR-4 grown by using a poised electrode as an electron acceptor. This approach detected redox-active molecules within biofilms, which were involved in electron transfer to the electrode. A combination of methods identified a mixture of riboflavin and riboflavin-5′-phosphate in supernatants from biofilm reactors, with riboflavin representing the dominant component during sustained incubations (>72 h). Removal of riboflavin from biofilms reduced the rate of electron transfer to electrodes by >70%, consistent with a role as a soluble redox shuttle carrying electrons from the cell surface to external acceptors. Differential pulse voltammetry and cyclic voltammetry revealed a layer of flavins adsorbed to electrodes, even after soluble components were removed, especially in older biofilms. Riboflavin adsorbed quickly to other surfaces of geochemical interest, such as Fe(III) and Mn(IV) oxy(hydr)oxides. This in situ demonstration of flavin production, and sequestration at surfaces, requires the paradigm of soluble redox shuttles in geochemistry to be adjusted to include binding and modification of surfaces. Moreover, the known ability of isoalloxazine rings to act as metal chelators, along with their electron shuttling capacity, suggests that extracellular respiration of minerals by Shewanella is more complex than originally conceived.
References
45
Referenced
1,716
10.1146/annurev.bi.65.070196.002541
10.1590/S0103-50532003000200008
10.1016/S0003-2670(99)00610-8
10.1128/AEM.71.8.4414-4426.2005
10.1080/01490450252864253
10.1038/35011098
10.1128/AEM.70.9.5415-5425.2004
10.1016/j.jinorgbio.2007.07.020
10.1073/pnas.0604517103
- A Albert, The metal-binding properties of riboflavin. Biochem J 47, xxvii (1950). / Biochem J / The metal-binding properties of riboflavin. by Albert A (1950)
10.1042/bj0540646
10.1128/JB.180.6.1473-1479.1998
10.1128/AEM.69.3.1548-1555.2003
10.1126/science.1066771
10.1002/bit.21671
10.1373/clinchem.2005.051169
- DH Park, BH Kim, Growth properties of the iron-reducing bacteria, Shewanella putrefaciens IR-1 and MR-1 coupling to reduction of Fe(III) to Fe(II). J Microbiol 39, 273–278 (2001). / J Microbiol / Growth properties of the iron-reducing bacteria, Shewanella putrefaciens IR-1 and MR-1 coupling to reduction of Fe(III) to Fe(II). by Park DH (2001)
10.1128/AEM.68.12.6256-6262.2002
10.1146/annurev.nutr.20.1.153
10.1128/AEM.68.4.1760-1771.2002
10.1074/jbc.275.12.8515
10.1007/s00775-007-0278-y
10.1128/AEM.72.2.1558-1568.2006
10.1016/j.bbabio.2006.04.002
10.1021/bi034789c
10.1021/ja980197j
10.1021/jp981023r
10.1023/A:1010316708080
10.1021/ja00078a030
10.1021/ic0483747
- AJ Bard, LR Faulkner Electrochemical Methods (Wiley, Hoboken, NJ, 2001). / Electrochemical Methods by Bard AJ (2001)
10.1590/S0103-50532002000500015
10.1128/AEM.01444-06
10.1021/ja9608611
10.1007/s00253-002-0972-1
10.1149/1.2189257
10.1128/AEM.70.9.5373-5382.2004
10.1007/BF02148213
10.1016/S0141-0229(01)00478-1
10.1346/CCMN.1984.0320405
10.1346/CCMN.1983.0310604
10.1007/s00425-006-0476-9
10.1002/jobm.200610279
10.1111/j.1365-2621.1982.tb10120.x
10.1128/AEM.01387-07
Dates
Type | When |
---|---|
Created | 17 years, 5 months ago (March 3, 2008, 8:54 p.m.) |
Deposited | 3 years, 4 months ago (April 12, 2022, 5:01 p.m.) |
Indexed | 13 hours, 29 minutes ago (Aug. 31, 2025, 6:04 a.m.) |
Issued | 17 years, 5 months ago (March 11, 2008) |
Published | 17 years, 5 months ago (March 11, 2008) |
Published Online | 17 years, 5 months ago (March 11, 2008) |
Published Print | 17 years, 5 months ago (March 11, 2008) |
@article{Marsili_2008, title={Shewanella secretes flavins that mediate extracellular electron transfer}, volume={105}, ISSN={1091-6490}, url={http://dx.doi.org/10.1073/pnas.0710525105}, DOI={10.1073/pnas.0710525105}, number={10}, journal={Proceedings of the National Academy of Sciences}, publisher={Proceedings of the National Academy of Sciences}, author={Marsili, Enrico and Baron, Daniel B. and Shikhare, Indraneel D. and Coursolle, Dan and Gralnick, Jeffrey A. and Bond, Daniel R.}, year={2008}, month=mar, pages={3968–3973} }