Evidence map›Paper›PMID 28935878›Full record

ArticleScientific reports2017

Old Yellow Enzyme homologues in Mucor circinelloides: expression profile and biotransformation.

Alice Romagnolo, Federica Spina, Anna Poli, Sara Risso, Bianca Serito, Michele Crotti, Daniela Monti, Elisabetta Brenna, Luisa Lanfranco, Giovanna Cristina Varese

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 36% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. A novel ene-reductase fromRSC advances · 2025
    Article
  2. The Family Keeps on Growing: Four Novel Fungal OYEs Characterized.International journal of molecular sciences · 2022
    Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Alice RomagnoloDepartment of Life Sciences and Systems Biology, University of Turin, viale P. A. Mattioli 25, 10125, Turin, Italy.ORCID 0000-0002-8502-0873
Federica SpinaDepartment of Life Sciences and Systems Biology, University of Turin, viale P. A. Mattioli 25, 10125, Turin, Italy.
Anna PoliDepartment of Life Sciences and Systems Biology, University of Turin, viale P. A. Mattioli 25, 10125, Turin, Italy.
Sara RissoDepartment of Life Sciences and Systems Biology, University of Turin, viale P. A. Mattioli 25, 10125, Turin, Italy.
Bianca SeritoDepartment of Life Sciences and Systems Biology, University of Turin, viale P. A. Mattioli 25, 10125, Turin, Italy.
Michele CrottiDepartment of Chemistry, Materials and Chemical Engineering "G. Natta", Politecnico di Milano, via L. Mancinelli 7, 20131, Milan, Italy.
Daniela MontiIstituto di Chimica del Riconoscimento Molecolare, CNR, Via M. Bianco 9, 20131, Milan, Italy.
Elisabetta BrennaDepartment of Chemistry, Materials and Chemical Engineering "G. Natta", Politecnico di Milano, via L. Mancinelli 7, 20131, Milan, Italy.
Luisa LanfrancoDepartment of Life Sciences and Systems Biology, University of Turin, viale P. A. Mattioli 25, 10125, Turin, Italy.
Giovanna Cristina VareseDepartment of Life Sciences and Systems Biology, University of Turin, viale P. A. Mattioli 25, 10125, Turin, Italy. cristina.varese@unito.it.
University of Turin · ITPolitecnico di Milano · ITInstitute of Chemistry of Molecular Recognition · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The reduction of C=C double bond, a key reaction in organic synthesis, is mostly achieved by traditional chemical methods. Therefore, the search for enzymes capable of performing this reaction is rapidly increasing. Old Yellow Enzymes (OYEs) are flavin-dependent oxidoreductases, initially isolated from Saccharomyces pastorianus. In this study, the presence and activation of putative OYE enzymes was investigated in the filamentous fungus Mucor circinelloides, which was previously found to mediate C=C reduction. Following an in silico approach, using S. pastorianus OYE1 amminoacidic sequence as template, ten putative genes were identified in the genome of M. circinelloides. A phylogenetic analysis revealed a high homology of McOYE1-9 with OYE1-like proteins while McOYE10 showed similarity with thermophilic-like OYEs. The activation of mcoyes was evaluated during the transformation of three different model substrates. Cyclohexenone, α-methylcinnamaldehyde and methyl cinnamate were completely reduced in few hours and the induction of gene expression, assessed by qRT-PCR, was generally fast, suggesting a substrate-dependent activation. Eight genes were activated in the tested conditions suggesting that they may encode for active OYEs. Their expression over time correlated with C=C double bond reduction.

Indexed as

Gene Expression ProfilingGene Expression Regulation, FungalBayes TheoremBiotransformationFungal ProteinsGenome, FungalIsoenzymesMucorNADPH DehydrogenasePhylogenySubstrate SpecificityFungal ProteinsIsoenzymesNADPH Dehydrogenase

Identifiers

PMID28935878
PMCPMC5608841
OpenAlexW2754097480

What OpenQuestion holds

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Registered trials

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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.