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Turning
Fungus into Fuel
Monday, May 5, 2008
Organism with a taste for
olive drab shows promise for greener energy
Hi-Res
Version
The
photos show a microscope image of the fungus Tricoderma
reesei growth filaments. In the image, proteins in fungal
cells are stained red, while chitin, a component of the cell
walls, is stained blue.
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Credit:
Mari Valkonen, VTT Technical Research Center, Finland
A spidery fungus with a
voracious appetite for military uniforms and canvas tents could
hold the key to improvements in the production of biofuels, a
team of government, academic and industry researchers has
announced.
In a paper published today in Nature
Biotechnology, researchers led by Los Alamos National
Laboratory and the U.S. Department of Energy Joint Genome
Institute announced that the genetic sequence of the fungus
Tricoderma reesei has uncovered important clues about how
the organism breaks down plant fibers into simple sugars. The
finding could unlock possibilities for industrial processes that
can more efficiently and cost effectively convert corn,
switchgrass and even cellulose-based municipal waste into
ethanol. Ethanol from waste products is a more-carbon-neutral
alternative to gasoline.
The fungus T. reesei rose
to dubious fame during World War II when military leaders
discovered it was responsible for rapid deterioration of clothing
and tents in the South Pacific. Named after Dr. Elwyn T. Reese,
who, with colleagues, originally isolated the hungry fungus, T.
reesei was later identified as a source of industrial enzymes
and a role model for the conversion of cellulose and
hemicellulose-plant fibers-into simple sugars.
The
organism uses enzymes it creates to break down human-indigestible
fibers of plants into the simplest form of sugar, known as a
monosaccharide. The fungus then digests the sugars as
food.
Researchers decoded the genetic sequence of T.
reesei in an attempt to discover why the deep green fungus
was so darned good at digesting plant cells. The sequence results
were somewhat surprising. Contrary to what one might predict
about the gene content of a fungus that can eat holes in tents,
T. reesei had fewer genes dedicated to the production of
cellulose-eating enzymes than its counterparts.
"We
were aware of T. reesei's reputation as producer of
massive quantities of degrading enzymes, however we were
surprised by how few enzyme types it produces, which suggested to
us that its protein secretion system is exceptionally efficient,"
said Los Alamos bioscientist Diego Martinez (also at the
University of New Mexico), the study's lead author. The
researchers believe that T. reesei's genome includes
"clusters" of enzyme-producing genes, a strategy that
may account for the organism's efficiency at breaking down
cellulose.
On an industrial scale, T. reesei could
be employed to secrete enzymes that can be purified and added
into an aqueous mixture of cellulose pulp and other materials to
produce sugar. The sugar can then be fermented by yeast to
produce ethanol.
"The sequencing of the Trichoderma
reesei genome is a major step towards using renewable
feedstocks for the production of fuels and chemicals," said
Joel Cherry, director of research activities in second-generation
biofuels for Novozymes, a collaborating institution in the study.
"The information contained in its genome will allow us to
better understand how this organism degrades cellulose so
efficiently and to understand how it produces the required
enzymes so prodigiously. Using this information, it may be
possible to improve both of these properties, decreasing the cost
of converting cellulosic biomass to fuels and chemicals."
Other
authors of the paper include: From JGI-LANL (at Los Alamos
National Laboratory) Thomas Brettin, David Bruce, Chris Detter,
Cheryl Kuske, Olga Chertkov, Melissa Jackson, Cliff Han, Monica
Misra, Nina Thayer, Ravi Barbote, and Gary Xie; from the JGI-PGF
(Production Genomics Facility in Walnut Creek, California):
Jarrod Chapman, Igor Grigoriev, Isaac Ho, Susan Lucas, Nicolas
Putnam, Paul Richardson, Daniel Rokhsar, Eddy Rubin, Asaf Salamov
and Astrid Terry; and Pacific Northwest National Laboratory's
Scott Baker and Jon Magnuson.
Other collaborating
institutions include the U.S. Department of Agriculture's Forest
Products Lab, Oregon State University, University of New Mexico,
TU-Vienna, Catholic University of Chile, VTT Finland, and
Universités d'Aix-Marseille I & II.
Source:
Los Alamos National Laboratory

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