PreprintCited by 5Machine Learning in BioinformaticsEnzyme Catalysis and ImmobilizationEnzyme Production and Characterization

EP-pred: A Machine Learning Tool for Bioprospecting Promiscuous Ester Hydrolases

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Xiang, Ruite, Fernandez-Lopez, Laura, Robles-Martin, Ana, Ferrer, Manuel, Guallar, Victor·2022·Preprints.org

Preprint — published as 10.3390/biom12101529 · Paper page

Abstract

When bioprospecting for novel industrial enzymes, substrate promiscuity is a desirable property that increases the reusability of the enzyme. Among industrial enzymes, ester hydrolases have great relevance for which the demand has not ceased to increase. However, the search for new substrate promiscuous ester hydrolases is not trivial since the mechanism behind this property is greatly influenced by the active site's structural and physicochemical characteristics. These characteristics must be computed from the 3D structure, which is rarely available, and expensive to measure, hence the need for a method that can predict promiscuity from a sequence alone. Here we report such a method called EP-pred, an ensemble binary classifier, that combines three machine learning algorithms: SVM, KNN, and a Linear model. EP-pred has been evaluated against the Lipase Engineering Database together with a hidden Markov approach leading to a final set of 10 sequences predicted to encode promiscuous esterases. Experimental results confirmed the validity of our method since all ten proteins were found to exhibit a broad substrate ambiguity.

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Authors
Xiang, R., Fernandez-Lopez, L., Robles-Martin, A., Ferrer, M., & Guallar, V.
Affiliations
  • Barcelona Supercomputing Center (ES)
  • Consejo Superior de Investigaciones Científicas (ES)
Venue
Preprints.org
Publisher
MDPI AG
Published
2022-09-07
OpenAlex
W4297825892
Cited by
5
References
2
Citations by year
2026: 2 · 2024: 1 · 2023: 1 · 2022: 1
Type
posted content
Language
en
Open access
Locations
  • Preprints.org (acceptedVersion, cc-by)
  • Zenodo (CERN European Organization for Nuclear Research) (submittedVersion, cc-by)
Funders
  • European Commission (10.13039/501100011033, 101000607, 13039/501100011033, 501100011033, HORIZON2020, /AEI/10.13039/501100011033, 101000327)
  • Ministerio de Ciencia e Innovación (PDC2021-121534-I00, .13039/501100011033, 10.13039, / AEI/10, PID2020-112758RB-I00, PID2019, 10.13039/501100011033/, PID2019-106370RB-I00/AEI/10.13039/501100011033, 501100011033, PID2020, I00/AEI/10.13039, PID2019-106370RB-I00, /AEI/10.13039/ 501100011033)
  • European Regional Development Fund (10.13039/501100011033, 13039/501100011033, AEI/10.13039/501100011033, 501100011033)
  • Agencia Estatal de Investigación (AEI//10.13039/501100011033/, PDC2021-121534-I00, 501100011033, 10.13039/501100011033, 13039, .13039/501100011033, 10.13039, PID2020-112758RB-I00, AEI/10, PID2019-106370RB-I00, I00/AEI/10.13039/501100011033, PID2019)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Machine Learning in Bioinformatics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Enzyme Catalysis and Immobilization
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Biotechnology › Enzyme Production and Characterization
Keywords
ester hydrolase, substrate promiscuity, support vector machine, k-nearest neighbors, industrial enzymes

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