Lignin is the double-edged sword of biofuels: if you are making cellulosic ethanol, you want less lignin because it blocks the breakdown of cellulose. If you are using pyrolytic methods, you want more lignin because lignin contains more energy than cellulose. Whether you wish to maximize or minimize lignin content, an understanding of lignin synthesis is essential and has proved elusive. Lignin is a key adaptation to life on land, as it strengthens plant cell walls thereby helping land plants stand upright and reinforcing the cell walls of the specialized water-conducting tubes that are another key adaptation to growth in terrestrial environments.
The lignin polymer is made up of a complex arrangement of subunits and its subunit composition differs among different species. For example, ferns and conifers have lignin composed mainly of p-hydroxyphenyl (H) and guaiacyl (G) lignin units. Flowering plants have H and G subunits, plus syringyl (S) subunits derived from sinapyl alcohol. Interestingly, S lignin is also found in some lycophytes, including the spikemoss Selaginella (photo). In research published this week in The Plant Cell, a team of researchers led by Clint Chapple of Purdue University showed that lignin synthesis proceeds along a different path in Selaginella. Their work centers on the characterization of the enzyme ferulate 5-hydroxylase (F5H); in flowering plants, this enzyme produces S lignin units from G lignin precursors. By comparing the Selaginella enzyme (Sm F5H) to the F5H from the model flowering plant Arabidopsis thaliana (At F5H), the authors found that Sm F5H could both catalyze the same reaction as At F5H and could also catalyze an additional reaction, acting on precursors of H lignin to form precursors to G and S lignin, and thereby bypassing four steps in angiosperm lignin synthesis. Indeed, transgenic expression of Sm F5H can restore normal lignin deposition to Arabidopsis p
|Contact: Jennifer Mach|
American Society of Plant Biologists