Evidence map›Paper›PMID 32683610›Full record

ArticlePlant molecular biology2020

The reconstruction and biochemical characterization of ancestral genes furnish insights into the evolution of terpene synthase function in the Poaceae.

Katrin Luck, Xinlu Chen, Ayla M Norris, Feng Chen, Jonathan Gershenzon, Tobias G Köllner

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Article in Plant molecular biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 24% of its field
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  4. Article
  5. Applications of ancestral sequence reconstruction for understanding the evolution of plant specialized metabolism.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Review
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  9. Functional Characterization of a (International journal of molecular sciences · 2023
    Article
  10. Article
  11. Article
  12. The Next Generation of Rice: Inter-SubspecificFrontiers in plant science · 2022
    Article
  13. Article
  14. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Katrin LuckDepartment of Biochemistry, Max Planck Institute for Chemical Ecology, Hans-Knöll Straße 8, 07745, Jena, Germany.
Xinlu ChenDepartment of Plant Sciences, University of Tennessee, Knoxville, TN, 37996, USA.
Ayla M NorrisGraduate School of Genome Science and Technology, University of Tennessee, Knoxville, TN, 37996, USA.
Feng ChenDepartment of Plant Sciences, University of Tennessee, Knoxville, TN, 37996, USA.
Jonathan GershenzonDepartment of Biochemistry, Max Planck Institute for Chemical Ecology, Hans-Knöll Straße 8, 07745, Jena, Germany.
Tobias G KöllnerDepartment of Biochemistry, Max Planck Institute for Chemical Ecology, Hans-Knöll Straße 8, 07745, Jena, Germany. koellner@ice.mpg.de.ORCID http://orcid.org/0000-0002-7037-904X
Max Planck Institute for Chemical Ecology · DEUniversity of Tennessee at Knoxville · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

key messageDistinct catalytic features of the Poaceae TPS-a subfamily arose early in grass evolution and the reactions catalyzed have become more complex with time. The structural diversity of terpenes found in nature is mainly determined by terpene synthases (TPS). TPS enzymes accept ubiquitous prenyl diphosphates as substrates and convert them into the various terpene skeletons by catalyzing a carbocation-driven reaction. Based on their sequence similarity, terpene synthases from land plants can be divided into different subfamilies, TPS-a to TPS-h. In this study, we aimed to understand the evolution and functional diversification of the TPS-a subfamily in the Poaceae (the grass family), a plant family that contains important crops such as maize, wheat, rice, and sorghum. Sequence comparisons showed that aside from one clade shared with other monocot plants, the Poaceae TPS-a subfamily consists of five well-defined clades I-V, the common ancestor of which probably originated very early in the evolution of the grasses. A survey of the TPS literature and the characterization of representative TPS enzymes from clades I-III revealed clade-specific substrate and product specificities. The enzymes in both clade I and II function as sesquiterpene synthases with clade I enzymes catalyzing initial C10-C1 or C11-C1 ring closures and clade II enzymes catalyzing C6-C1 closures. The enzymes of clade III mainly act as monoterpene synthases, forming cyclic and acyclic monoterpenes. The reconstruction and characterization of clade ancestors demonstrated that the differences among clades I-III were already present in their ancestors. However, the ancestors generally catalyzed simpler reactions with less double-bond isomerization and fewer cyclization steps. Overall, our data indicate an early origin of key enzymatic features of TPS-a enzymes in the Poaceae, and the development of more complex reactions over the course of evolution.

Indexed as

Alkyl and Aryl TransferasesCloning, MolecularEscherichia coliEvolution, MolecularGenes, PlantIntramolecular LyasesPlant ProteinsPoaceaeSequence AnalysisTerpenesAlkyl and Aryl TransferasesIntramolecular Lyasespinene cyclase IPlant ProteinsTerpenesterpene synthaseAncestral sequence reconstructionEvolutionGrassesMaizeTerpene synthase

Identifiers

PMID32683610
PMCPMC7417412
OpenAlexW3043660882

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.