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Flowing electrons help ocean microbe gulp methane.





Pictured is a high magnification image of sediment enriched in syntrophic consortia. In the center of the image is an overview of sediment containing cells, and individual -- roughly spherical -- microbial communities are shown at high magnification at the ends of lines extending from the center. Fluorescent signals show the ANME-2c archaeal subgroup in red, and sulfate reducing bacteria are shown in green. Sediment particles appear yellow.
Credit: Grayson Chadwick/Caltech


Good communication is very crucial to any relationship, especially when partners are separated by distance. This also holds for microbes in the deep sea that need to work together to consume large amount of methane released from the vents on the ocean floors.
Recent work has shown that these microbes can still accomplish their task even if they are not attached together; they use electrons to share energy over long distances, this was done by Caltech University.
This is the first time that directs interspecies electron transport—the movement of electrons from a cell, through the external environment, to another cell type—has been documented in microorganisms in nature.
The results were published in September 16 issue of the Journal nature.
“Our lab is interested in microbial communities in the environment and, specifically, the symbiosis of mutually beneficial relationship,” says Professor of geobiology Victoria Orphan. For the last decade, Orphan’s lab has focused on the relationship between the species of bacteria and a species of archea that lives in symbiotic aggregates with deep sea methane seeps. The organisms work together in syntrophy—meaning they feed together—to consume up-to 80 percent of methane emitted from the ocean floor---methane that could be otherwise contributing to climate change as a greenhouse gas in our atmosphere.
Because these microbes grow slowly, reproducing twice per year, and live closest with each other, it has been difficult for researchers to isolate them for the environment to grow them in the labs. So, the Caltech team used research submersible, called Alivin, to collect samples containing the methane-oxidizing microbial consortia from deep-ocean methane seep sediments and then brought them back to the lab for analysis.
The researchers used different fluorescent DNA stains to mark two types of microbes and view their spatial orientation in consortia. In some consortia, Orphan and her colleagues found the bacterial and archaea cells were mixed, while other consortia, cells of the same type were clustered into separate areas.
They wondered if the variation in the spatial organization of the bacteria and archaea within the consortia influenced their cellular activities and their ability to cooperatively consume methane.
To find out, they applied a stable isotope “tracer” to evaluate metabolic activities.  The amount of isotope taken by individual archael and bacteria cells within their microbial neighborhood in each consortium was then measured within high-resolution instrument called nanoscale secondary mass spectrometry as Caltech. This helped the researchers to determine how active the archaeal  and bacteria partners were relative to their distance to one another.
To their surprise, the researchers found that the spatial arrangement of the cells in consortia had no influence on their activity.
To find out how the bacteria and archaea were partnering, co-first authors Grayson Shadwick looked for patterns in cellular activity for multiple consortia with different cell arrangement. They found that the populations of the syntrophic archaea and bacteria in consortia had similar levels of metabolic activity, the associated partner microorganism were also equally active.
To determine how these metabolic interactions were taking place even over relatively long distances, postdoctoral scholar and coauthor Chris Kempes, modeled the predicted relationship between cellular activity and distance between syntrophic partners that are dependent on the molecular diffusion of the substrate.  He found that the conventional metabolites were inconsistent with the spatial activity patterns observed in the data. However, revised models indicated that electrons could likely make the trip from cell to cell across greater distances.
Using genome analysis—along with transmission electron microscopy and a strain that reacts with these multi-heme cytohromes –the researchers showed that these conductive proteins were also present on the outer surface of the archaea they were studying. And that finding, Orphan says, can explain why the spatial arrangement partners do not seem to affect their relationship or activity.
Orphan said that the information they have learned about this relationship will help expand how researchers think and interspecies microbial interactions in nature. In addition, the microscale stable isotope used in the current study can be used to evaluate interspecies electron transport and other forms of microbial symbiosis occurring in the environment.

Credit: California Institute of Technology.
Material can be edited for content and length.
Ed Tesla

Ed Tesla

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