Evidence map›Paper›PMID 41855221›Full record

ArticlePLoS computational biology2026

PHA synthase variant design using a conditional variational autoencoder.

Tuula Tenkanen, Anna Ylinen, Paula Jouhten, Merja Penttilä, Sandra Castillo

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Article in PLoS computational biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Tuula TenkanenVTT Technical Research Centre of Finland Ltd., Espoo, Finland.ORCID https://orcid.org/0009-0003-7311-1975
Anna YlinenVTT Technical Research Centre of Finland Ltd., Espoo, Finland.
Paula JouhtenDepartment of Bioproducts and Biosystems, Aalto University, Espoo, Finland.ORCID https://orcid.org/0000-0003-1075-7448
Merja PenttiläVTT Technical Research Centre of Finland Ltd., Espoo, Finland.
Sandra CastilloVTT Technical Research Centre of Finland Ltd., Espoo, Finland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polyhydroxyalkanoate (PHA) synthases are a group of complex, dimeric enzymes which catalyze polymerization of R-hydroxyacids into PHAs. PHA properties depend on their monomer composition but enzymes found in nature have limited specificities to certain R-hydroxyacids only. In this study, a conditional variational autoencoder was used for the first time to design novel PHA synthases. The model was trained with native protein sequences obtained from Uniprot and was used for the creation of approximately 10 000 new PHA synthase enzymes. Out of these, 16 sequences were selected for in vivo validation. The selection criteria included the presence of conserved residues such as catalytic amino acids and amino acids in the dimer interface and structural features like the number of [Formula: see text]-helices in the N-terminal part of the enzyme. Two of the 16 novel PHA synthases that had substantial numbers of amino acid substitutions (87 and 98) with respect to the most similar native enzymes were confirmed active and produced poly(hydroxybutyrate) (PHB) when expressed in yeast S. cerevisiae. The results show the power of AI based methods to create active variants of highly complex dimer enzymes.

Indexed as

AcyltransferasesProtein EngineeringAmino Acid SequenceAutoencoderComputational BiologyModels, MolecularSaccharomyces cerevisiaeAcyltransferasespoly(3-hydroxyalkanoic acid) synthase

Identifiers

PMID41855221
PMCPMC13020758

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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.