Researchers reproduce evolutionary path with designer lignin
When scientists reported in 2014 that they had successfully engineered a poplar plant “designed for deconstruction,” the finding made international news. The highly degradable poplar, the first of its kind, could substantially reduce the energy use and cost of converting biomass to a number of products, including biofuels, pulp and paper.
Now, some of those same researchers are reporting a surprising new revelation. As University of Wisconsin–Madison biochemistry Professor John Ralph puts it, “Nature was already doing what we thought we’d laboriously taught her to do.”
To make the hybrid poplar, Ralph, Shawn Mansfield, Curtis Wilkerson, and other Great Lakes Bioenergy Research Center researchers had incorporated an exotic gene conferring weak bonds into the plant’s lignin, the hard-to-process compound that gives plant cell walls their sturdiness but makes them difficult to process in an industrial setting. The resulting lignin, dubbed zip-lignin, readily breaks down under simple chemical conditions.
This new GLBRC-led study, published Oct. 14 in Science Advances, shows that those poplar trees and many other plants from all over the phylogenetic tree have actually evolved to naturally produce zip-lignin. In other words, not only can we potentially breed for degradability in plants, but humans may have been doing just that—selecting certain plants for easier processing—for thousands of years.
“We didn’t know the plants were making the native zip because we couldn’t detect it,” says Steve Karlen, a research scientist at UW–Madison and the paper’s lead author. “When we added the new gene we thought we were adding functionality, but we were actually increasing what was already there.”
Even though the team couldn’t at first detect native zip-lignin in poplar trees or in angelica, the Chinese herb from which the group had taken the gene, its absence did raise some questions. Ralph had long suspected that some plant somewhere was naturally creating zip-lignin. And Karlen wondered how angelica, or any plant for that matter, could be making the molecules that confer weak bonds in lignin but not incorporate them.
Using a method that Ralph’s group had developed decades ago, plus a new and highly sensitive mass spectrometer, Karlen sharpened his focus, finding a way to detect low levels of native zip-lignin in poplar trees. With the help of Philip Harris, a professor of biological sciences at the University of Auckland in New Zealand, Karlen began a full-scale phylogenic study, seeking to determine what other plants might contain native zip-lignin.
Karlen was soon elbow-deep in greenhouses, gardens and landscaping beds all over the UW–Madison campus. Examining the more than 60 plant samples brought back to the lab revealed that zip-lignin is found in an exceptionally diverse array of plants: in balsa, in birds of paradise, in all the grasses he sampled, and in about half of the hardwoods, to name just a few.
With collaborator Laura Bartley, an associate professor of microbiology and plant biology at the University of Oklahoma, Karlen also found zip-lignin in rice. Since an entirely different gene was responsible for making this lignin, the team determined that plants have independently evolved to make zip-lignin, essentially developing a common feature through entirely different means.
Although Karlen and his collaborators don’t yet know what the evolutionary advantage of native zip-lignin might be for plants, its widespread presence broadens the scope of their research and holds out the possibility of increasing, either through engineering or breeding, the degradability of a surprisingly vast array of plants.
“The fact that natural plants are already doing this means there are a lot more genes available for doing this than we knew about,” says Ralph. “And that means a much broader opportunity to learn from and take advantage of what these natural plants are already doing.”