4.8 Article

Visualization of plant cell wall lignification using fluorescence-tagged monolignols

Journal

PLANT JOURNAL
Volume 76, Issue 3, Pages 357-366

Publisher

WILEY
DOI: 10.1111/tpj.12299

Keywords

Arabidopsis thaliana; cell wall; dehydrogenative polymerization; fluorescence microscopy; fluorescent probes; lignin; Pinus radiata; technical advance

Categories

Funding

  1. US Department of Energy, the Office of Science [DE-SC0006930]
  2. University of Wisconsin Vilas Associate Award
  3. Stanford University Global Climate and Energy Project (GCEP)
  4. Scion CORE
  5. Great Lakes Bioenergy Research Center (GLBRC)
  6. Joint BioEnergy Institute (JBEI)
  7. Center for Direct Catalytic Conversion of Biomass to Biofuels (C3Bio), an Energy Frontier Research Center
  8. US DOE's Office of Science [DE-FC02-07ER64494, DE-AC02-05CH11231, DE-SC0000997]
  9. Japan Society for the Promotion of Science (JSPS)
  10. U.S. Department of Energy (DOE) [DE-SC0006930] Funding Source: U.S. Department of Energy (DOE)

Ask authors/readers for more resources

Lignin is an abundant phenylpropanoid polymer produced by the oxidative polymerization of p-hydroxycinnamyl alcohols (monolignols). Lignification, i.e., deposition of lignin, is a defining feature of secondary cell wall formation in vascular plants, and provides an important mechanism for their disease resistance; however, many aspects of the cell wall lignification process remain unclear partly because of a lack of suitable imaging methods to monitor the process in vivo. In this study, a set of monolignol analogs -linked to fluorogenic aminocoumarin and nitrobenzofuran dyes were synthesized and tested as imaging probes to visualize the cell wall lignification process in Arabidopsis thaliana and Pinus radiata under various feeding regimens. In particular, we demonstrate that the fluorescence-tagged monolignol analogs can penetrate into live plant tissues and cells, and appear to be metabolically incorporated into lignifying cell walls in a highly specific manner. The localization of the fluorogenic lignins synthesized during the feeding period can be readily visualized by fluorescence microscopy and is distinguishable from the other wall components such as polysaccharides as well as the pre-existing lignin that was deposited earlier in development.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available