Fake Shewanella Reveals How Bacteria Breathe Iron
Certain bacteria can breathe iron like we breathe oxygen. Understanding how they do so will help researchers use the microbes for cleaning up soil contaminants, for trapping carbon dioxide or for making batteries out of bacteria.
Electrons conduct through bacterial proteins directly to minerals containing iron
Findings published today in the journal Proceedings of the National Academy of Sciences (PNAS) show that proteins on the surface of bacteria can produce an electric current by simply touching a mineral surface.
The research shows that it is possible for bacteria to lie directly on the surface of a metal or mineral and transfer electrical charge through their cell membranes. This means that it is possible to ‘tether’ bacteria directly to electrodes – bringing scientists a step closer to creating efficient microbial fuel cells or ‘bio-batteries.’
The team collaborated with researchers at Pacific Northwest National Laboratory in Washington State in the US. The project was funded by the Biotechnology and Biological Sciences Research Council (BBSRC) and the US Department of Energy.
Shewanella oneidensis (pictured) is part of a family of marine bacteria. The research team created a synthetic version of this bacteria using just the proteins thought to shuttle the electrons from the inside of the microbe to the rock.
They inserted these proteins into the lipid layers of vesicles, which are small capsules of lipid membranes such as the ones that make up a bacterial membrane. Then they tested how well electrons travelled between an electron donor on the inside and an iron-bearing mineral on the outside.
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| Shewanella oneidensis are bacteria that live off of minerals such as hematite, shown here, where they use iron like people use oxygen. Metal-breathing bacteria can be used to immobilize radioactive contaminants in soil. Image courtesy of Pacific Northwest National Laboratory |
Lead researcher Dr Tom Clarke from University of East Anglia’s school of Biological Sciences said: “We knew that bacteria can transfer electricity into metals and minerals, and that the interaction depends on special proteins on the surface of the bacteria. But it was not been clear whether these proteins do this directly or indirectly though an unknown mediator in the environment.
“Our research shows that these proteins can directly 'touch' the mineral surface and produce an electric current, meaning that is possible for the bacteria to lie on the surface of a metal or mineral and conduct electricity through their cell membranes.
“This is the first time that we have been able to actually look at how the components of a bacterial cell membrane are able to interact with different substances, and understand how differences in metal and mineral interactions can occur on the surface of a cell.
“These bacteria show great potential as microbial fuel cells, where electricity can be generated from the breakdown of domestic or agricultural waste products.
“Another possibility is to use these bacteria as miniature factories on the surface of an electrode, where chemicals reactions take place inside the cell using electrical power supplied by the electrode through these proteins.”
Biochemist Liang Shi of Pacific Northwest National Laboratory said: "We developed a unique system so we could mimic electron transfer like it happens in cells. The electron transfer rate we measured was unbelievably fast - it was fast enough to support bacterial respiration."
The finding is also important for understanding how carbon works its way through the atmosphere, land and oceans.
"When organic matter is involved in reducing iron, it releases carbon dioxide and water. And when iron is used as an energy source, bacteria incorporate carbon dioxide into food. If we understand electron transfer, we can learn how bacteria controls the carbon cycle," said Shi.
‘Rapid electron exchange between surface-exposed bacterial cytochromes and Fe(III) minerals’ by Thomas A Clarke, Gaye White, Julea N Butt, and David J Richardson (all UEA, UK), and Zhri Shi, Liang Shi, Zheming Wang, Alice C Dohnalkova, Matthew J Marshall, James K Fredrickson and John M Zachara (all PNNL, USA) is published by PNAS on Monday, March 25.