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Genome assembly of Chiococca alba uncovers key enzymes involved in the biosynthesis of unusual terpenoids.
Lau, Kin H; Bhat, Wajid Waheed; Hamilton, John P; Wood, Joshua C; Vaillancourt, Brieanne; Wiegert-Rininger, Krystle; Newton, Linsey; Hamberger, Britta; Holmes, Daniel; Hamberger, Bjoern; Buell, C Robin.
Affiliation
  • Lau KH; Department of Plant Biology.
  • Bhat WW; Department of Biochemistry and Molecular Biology.
  • Hamilton JP; Department of Plant Biology.
  • Wood JC; Department of Plant Biology.
  • Vaillancourt B; Department of Plant Biology.
  • Wiegert-Rininger K; Department of Plant Biology.
  • Newton L; Department of Plant Biology.
  • Hamberger B; Department of Biochemistry and Molecular Biology.
  • Holmes D; Department of Chemistry.
  • Hamberger B; Department of Biochemistry and Molecular Biology.
  • Buell CR; MSU AgBioResearch.
DNA Res ; 27(3)2020 Jun 01.
Article in En | MEDLINE | ID: mdl-32642754
ABSTRACT
Chiococca alba (L.) Hitchc. (snowberry), a member of the Rubiaceae, has been used as a folk remedy for a range of health issues including inflammation and rheumatism and produces a wealth of specialized metabolites including terpenes, alkaloids, and flavonoids. We generated a 558 Mb draft genome assembly for snowberry which encodes 28,707 high-confidence genes. Comparative analyses with other angiosperm genomes revealed enrichment in snowberry of lineage-specific genes involved in specialized metabolism. Synteny between snowberry and Coffea canephora Pierre ex A. Froehner (coffee) was evident, including the chromosomal region encoding caffeine biosynthesis in coffee, albeit syntelogs of N-methyltransferase were absent in snowberry. A total of 27 putative terpene synthase genes were identified, including 10 that encode diterpene synthases. Functional validation of a subset of putative terpene synthases revealed that combinations of diterpene synthases yielded access to products of both general and specialized metabolism. Specifically, we identified plausible intermediates in the biosynthesis of merilactone and ribenone, structurally unique antimicrobial diterpene natural products. Access to the C. alba genome will enable additional characterization of biosynthetic pathways responsible for health-promoting compounds in this medicinal species.
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Full text: 1 Database: MEDLINE Main subject: Terpenes / Rubiaceae Language: En Journal: DNA Res Year: 2020 Type: Article

Full text: 1 Database: MEDLINE Main subject: Terpenes / Rubiaceae Language: En Journal: DNA Res Year: 2020 Type: Article