4.8 Article

Caffeoyl Shikimate Esterase (CSE) Is an Enzyme in the Lignin Biosynthetic Pathway in Arabidopsis

Journal

SCIENCE
Volume 341, Issue 6150, Pages 1103-1106

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1241602

Keywords

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Funding

  1. European Commission [211982, 270089]
  2. Stanford University's Global Climate and Energy Project
  3. Hercules program of Ghent University for the Synapt Q-Tof [AUGE/014]
  4. Bijzonder Onderzoeksfonds-Zware Apparatuur of Ghent University [174PZA05]
  5. Ghent University [01MRB510W]
  6. Research Foundation-Flanders
  7. Agency for Innovation by Science and Technology (IWT)
  8. CAPES-Brazil [201660/2010-5]
  9. CNPq-Brazil [201998/2011-4]
  10. U.S. Department of Energy's Great Lakes Bioenergy Research Center (DOE Office of Science) [BER DE-FC02-07ER64494]
  11. Scottish Government
  12. Science Advisory Board of the NSF [DBI-0922391]
  13. BBSRC [BB/G016232/1] Funding Source: UKRI
  14. Biotechnology and Biological Sciences Research Council [BB/G016232/1] Funding Source: researchfish

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Lignin is a major component of plant secondary cell walls. Here we describe caffeoyl shikimate esterase (CSE) as an enzyme central to the lignin biosynthetic pathway. Arabidopsis thaliana cse mutants deposit less lignin than do wild-type plants, and the remaining lignin is enriched in p-hydroxyphenyl units. Phenolic metabolite profiling identified accumulation of the lignin pathway intermediate caffeoyl shikimate in cse mutants as compared to caffeoyl shikimate levels in the wild type, suggesting caffeoyl shikimate as a substrate for CSE. Accordingly, recombinant CSE hydrolyzed caffeoyl shikimate into caffeate. Associated with the changes in lignin, the conversion of cellulose to glucose in cse mutants increased up to fourfold as compared to that in the wild type upon saccharification without pretreatment. Collectively, these data necessitate the revision of currently accepted models of the lignin biosynthetic pathway.

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