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Molecular Diversity of Terpene Synthases in the Liverwort Marchantia polymorpha.
Kumar, Santosh; Kempinski, Chase; Zhuang, Xun; Norris, Ayla; Mafu, Sibongile; Zi, Jiachen; Bell, Stephen A; Nybo, Stephen Eric; Kinison, Scott E; Jiang, Zuodong; Goklany, Sheba; Linscott, Kristin B; Chen, Xinlu; Jia, Qidong; Brown, Shoshana D; Bowman, John L; Babbitt, Patricia C; Peters, Reuben J; Chen, Feng; Chappell, Joe.
Affiliation
  • Kumar S; Plant Biology Program and Department of Pharmaceutical Sciences, University of Kentucky, Lexington, Kentucky 40536-0082.
  • Kempinski C; Plant Biology Program and Department of Pharmaceutical Sciences, University of Kentucky, Lexington, Kentucky 40536-0082.
  • Zhuang X; Plant Biology Program and Department of Pharmaceutical Sciences, University of Kentucky, Lexington, Kentucky 40536-0082.
  • Norris A; Gradaute School of Genome Science and Technology, University of Tennessee, Knoxville, Tennessee 37996-0840.
  • Mafu S; Roy J. Carver Department of Biochemistry, Biophysics, and Molecular Biology, Iowa State University, Ames, Iowa 50011.
  • Zi J; Roy J. Carver Department of Biochemistry, Biophysics, and Molecular Biology, Iowa State University, Ames, Iowa 50011.
  • Bell SA; Plant Biology Program and Department of Pharmaceutical Sciences, University of Kentucky, Lexington, Kentucky 40536-0082.
  • Nybo SE; Plant Biology Program and Department of Pharmaceutical Sciences, University of Kentucky, Lexington, Kentucky 40536-0082.
  • Kinison SE; Plant Biology Program and Department of Pharmaceutical Sciences, University of Kentucky, Lexington, Kentucky 40536-0082.
  • Jiang Z; Plant Biology Program and Department of Pharmaceutical Sciences, University of Kentucky, Lexington, Kentucky 40536-0082.
  • Goklany S; Plant Biology Program and Department of Pharmaceutical Sciences, University of Kentucky, Lexington, Kentucky 40536-0082.
  • Linscott KB; Plant Biology Program and Department of Pharmaceutical Sciences, University of Kentucky, Lexington, Kentucky 40536-0082.
  • Chen X; Department of Plant Sciences, University of Tennessee, Knoxville, Tennessee 37996-4561.
  • Jia Q; Gradaute School of Genome Science and Technology, University of Tennessee, Knoxville, Tennessee 37996-0840.
  • Brown SD; Departments of Bioengineering and Therapeutic Sciences and Pharmaceutical Chemistry, California Institute for Quantitative Biosciences, University of California, San Francisco, California 94158-2330.
  • Bowman JL; School of Biological Sciences, Monash University, Melbourne, VIC 3800, Australia.
  • Babbitt PC; Departments of Bioengineering and Therapeutic Sciences and Pharmaceutical Chemistry, California Institute for Quantitative Biosciences, University of California, San Francisco, California 94158-2330.
  • Peters RJ; Roy J. Carver Department of Biochemistry, Biophysics, and Molecular Biology, Iowa State University, Ames, Iowa 50011.
  • Chen F; Gradaute School of Genome Science and Technology, University of Tennessee, Knoxville, Tennessee 37996-0840.
  • Chappell J; Department of Plant Sciences, University of Tennessee, Knoxville, Tennessee 37996-4561.
Plant Cell ; 28(10): 2632-2650, 2016 10.
Article in En | MEDLINE | ID: mdl-27650333
Marchantia polymorpha is a basal terrestrial land plant, which like most liverworts accumulates structurally diverse terpenes believed to serve in deterring disease and herbivory. Previous studies have suggested that the mevalonate and methylerythritol phosphate pathways, present in evolutionarily diverged plants, are also operative in liverworts. However, the genes and enzymes responsible for the chemical diversity of terpenes have yet to be described. In this study, we resorted to a HMMER search tool to identify 17 putative terpene synthase genes from M. polymorpha transcriptomes. Functional characterization identified four diterpene synthase genes phylogenetically related to those found in diverged plants and nine rather unusual monoterpene and sesquiterpene synthase-like genes. The presence of separate monofunctional diterpene synthases for ent-copalyl diphosphate and ent-kaurene biosynthesis is similar to orthologs found in vascular plants, pushing the date of the underlying gene duplication and neofunctionalization of the ancestral diterpene synthase gene family to >400 million years ago. By contrast, the mono- and sesquiterpene synthases represent a distinct class of enzymes, not related to previously described plant terpene synthases and only distantly so to microbial-type terpene synthases. The absence of a Mg2+ binding, aspartate-rich, DDXXD motif places these enzymes in a noncanonical family of terpene synthases.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Alkyl and Aryl Transferases / Marchantia Language: En Journal: Plant Cell Journal subject: BOTANICA Year: 2016 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Alkyl and Aryl Transferases / Marchantia Language: En Journal: Plant Cell Journal subject: BOTANICA Year: 2016 Type: Article