BOSTON, Mass. (Mar. 4, 2010) ≠ Reduce. Reuse. Recycle. We hear this mantra time and again. When it comes to carbončthe "Most Wanted" element in terms of climate changečnature has got reuse and recycle covered. However, it's up to us to reduce. Scientists at Harvard Medical School are trying to meet this challenge by learning more about the carbon cycle, that is, the process by which carbon moves from the atmosphere into plants, oceans, soils, the earth's crust, and back into the atmosphere again.
One of the biggest movers and shakers is the lowly cyanobacteria, an ocean-dwelling, one-celled organism. Pamela Silver, HMS professor of systems biology, and colleagues have uncovered details about how this bacteria fixes, or digests, carbon. These bacteria build miniature factories inside themselves that turn carbon into fuel.
Silver and her colleagues report that the bacteria organize these factories spatially, revealing a structural sophistication not often seen in single-celled organisms. This regular and predictable spacing improves the efficiency of carbon processing. In the future, an understanding of the mechanisms that govern this spatial organization may help improve the efficiency of designer bacteria engineered to produce carbon-neutral fuels such as biodiesel and hydrogen.
These findings will be published online March 5 in the journal Science.
The rod-shaped cyanobacteria are among the most abundant organisms on earth. Forty percent of the carbon in the carbon cycle is reused and recycled through these tiny creatures. To process carbon, cyanobacteria build soccer-ball-shaped structures inside themselves called carboxysomes. These tiny factories absorb carbon dioxide and convert it into sugar, which the bacteria then use to produce energy.
"The ocean is just packed with these bacteria. By studying them, we're understanding more about how the earth works," said Silver, who is also on the faculty of the Wyss Institute for Biologically Inspired Engineering at HMS. "I'm blown away by what's happening in the ocean and what we don't understand about it. There are a lot of things in the ocean that are going to be useful to us."
The research team, led by co-first authors, research fellows David Savage and Bruno Afonso, attached a fluorescent tag to proteins involved in building the carboxysome, then grew the tagged bacteria under a microscope.
The resulting images revealed that, instead of being randomly numbered and haphazardly placed, cyanobacteria build carboxysomes in numbers that scale with their size, and they space the factories evenly along their length. (see image, end of release)
The finding adds evidence for new ways to think about bacteria. "We had this idea of bacteria as a bag of enzymes, but that has been completely shattered," said Afonso. A single protein, called parA, acts as a kind of inner-bacterium stage manager, arranging the carboxysomes in a neat, single-file row, the researchers found. When they disabled the bacteria's ability to make the protein, the carboxysomes were distributed far more randomly.
The cyanobacteria lacking parA were also less "fit" for survival, said Savage. While wild-type bacteria cells have a consistent number of carboyxsomes, which in turn optimizes carbon processing and fitness, the knockout bacterium created daughter cells whose numbers of carboxysomes ranged from none to an excess. The daughter cells with few or no carboxysomes divide more slowly and also process fifty percent less carbon than daughter cells at the other end of the spectrum. (see video 1)
By tagging parA in wild-type bacteria, they discovered interesting dynamics in the protein. Thousands of parA proteins repeatedly cluster together and shoot quickly from one end of the bacterium to the other. (see video 2)
"It's amazing that you can generate this regularity and symmetry potentially from a single protein," said Savage. "It's amazing that it is somehow tuned by the dynamics of the protein." The researchers have not yet identified the exact mechanism parA uses to govern the spacing.
Many other bacteria also have the parA protein, which is known for separating chromosomes during cell division. "This work highlights how bacteria cobble together spare parts to achieve similar goals such as organization and segregation," said David Rudner, HMS assistant professor of microbiology and molecular genetics, who was not involved in the study.
These findings may help synthetic biologists one day create designer bacteria.
"Knowledge about how cells create and deploy specialized factories like the carboxysome opens the way to creating other kinds of mini factories that could perform useful functions," said Richard Losick, Harvard University professor of molecular and cellular biology, who was not involved in the study.
Silver's lab is looking into whether the carboxysome might be useful for optimizing the production of hydrogen by engineered bacteria. One challenge in designing hydrogen-producing bacteria is that the enzymes that produce hydrogen are sensitive to oxygen. The carboxysome may help solve this problem because its outer shell blocks out oxygen, protecting the enzymes inside from its toxic effects.
This research was funded by the US Army Research Office.
Written by Elizabeth Dougherty
Image: Fluorescent labeling of proteins inside the carboxysome show that
cyanobacteria create carboxysomes in numbers proportional to length and
space them evenly along their longest axis.
Video 1: Knock-out bacteria, like the ones shown here who lack in parA, are
less fit for survival. While wild-type bacteria cells have a consistent
number of carboyxsomes, the knockouts either don't have enough or have too
many, which leads to slower cell division and less carbon processing.
Video 2: Green tagged parA proteins gather at one side of the bacterium,
shoot to the other end as a cluster, then shoot back. This dynamic seems to
be associated with the even spacing of carboxysomes.
Science, 5 March 2010, Vol 327, Issue 5970
"Spatially Ordered Dynamics of the Bacterial Carbon Fixation Machinery"
David F. Savage, Bruno Afonso, Anna Chen, and Pamela A. Silver
Department of Systems Biology, Harvard Medical School, Boston, MA, USA 02115, USA
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