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Integrating structure-based machine learning and co-evolution to investigate specificity in plant sesquiterpene synthases

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  • Janani Durairaj
  • Elena Melillo
  • Harro J Bouwmeester
  • Jules Beekwilder
  • Dick de Ridder
  • Aalt D J van Dijk

Abstract

Sesquiterpene synthases (STSs) catalyze the formation of a large class of plant volatiles called sesquiterpenes. While thousands of putative STS sequences from diverse plant species are available, only a small number of them have been functionally characterized. Sequence identity-based screening for desired enzymes, often used in biotechnological applications, is difficult to apply here as STS sequence similarity is strongly affected by species. This calls for more sophisticated computational methods for functionality prediction. We investigate the specificity of precursor cation formation in these elusive enzymes. By inspecting multi-product STSs, we demonstrate that STSs have a strong selectivity towards one precursor cation. We use a machine learning approach combining sequence and structure information to accurately predict precursor cation specificity for STSs across all plant species. We combine this with a co-evolutionary analysis on the wealth of uncharacterized putative STS sequences, to pinpoint residues and distant functional contacts influencing cation formation and reaction pathway selection. These structural factors can be used to predict and engineer enzymes with specific functions, as we demonstrate by predicting and characterizing two novel STSs from Citrus bergamia.Author summary: Predicting enzyme function is a popular problem in the bioinformatics field that grows more pressing with the increase in protein sequences, and more attainable with the increase in experimentally characterized enzymes. Terpenes and terpenoids form the largest classes of natural products and find use in many drugs, flavouring agents, and perfumes. Terpene synthases catalyze the biosynthesis of terpenes via multiple cyclizations and carbocation rearrangements, generating a vast array of product skeletons. In this work, we present a three-pronged computational approach to predict carbocation specificity in sesquiterpene synthases, a subset of terpene synthases with one of the highest diversities of products. Using homology modelling, machine learning and co-evolutionary analysis, our approach combines sparse structural data, large amounts of uncharacterized sequence data, and the current set of experimentally characterized enzymes to provide insight into residues and structural regions that likely play a role in determining product specificity. Similar techniques can be re-purposed for function prediction and enzyme engineering in many other classes of enzymes.

Suggested Citation

  • Janani Durairaj & Elena Melillo & Harro J Bouwmeester & Jules Beekwilder & Dick de Ridder & Aalt D J van Dijk, 2021. "Integrating structure-based machine learning and co-evolution to investigate specificity in plant sesquiterpene synthases," PLOS Computational Biology, Public Library of Science, vol. 17(3), pages 1-21, March.
  • Handle: RePEc:plo:pcbi00:1008197
    DOI: 10.1371/journal.pcbi.1008197
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    References listed on IDEAS

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    1. Yasuo Yoshikuni & Thomas E. Ferrin & Jay D. Keasling, 2006. "Designed divergent evolution of enzyme function," Nature, Nature, vol. 440(7087), pages 1078-1082, April.
    2. Melissa Salmon & Caroline Laurendon & Maria Vardakou & Jitender Cheema & Marianne Defernez & Sol Green & Juan A. Faraldos & Paul E. O’Maille, 2015. "Emergence of terpene cyclization in Artemisia annua," Nature Communications, Nature, vol. 6(1), pages 1-10, May.
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