Evidence map›Paper›PMID 30866798›Full record

ArticleBMC evolutionary biology2019

New insights on unspecific peroxygenases: superfamily reclassification and evolution.

Muniba Faiza, Shengfeng Huang, Dongming Lan, Yonghua Wang

Abstract read
In one paragraph

Article in BMC evolutionary biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

21 citing papers in PubMed.

  1. Genome-Wide Analysis ofJournal of fungi (Basel, Switzerland) · 2026
    Article
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  6. Review
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  8. Recent advances in fungal xenobiotic metabolism: enzymes and applications.World journal of microbiology & biotechnology · 2023
    Review
  9. Article
  10. Article
  11. EngineeringAntioxidants (Basel, Switzerland) · 2022
    Article
  12. Review
  13. Review
  14. Chromoselective Photocatalysis Enables Stereocomplementary Biocatalytic Pathways.Angewandte Chemie (Weinheim an der Bergstrasse, Germany) · 2021
    Article
  15. Chromoselective Photocatalysis Enables Stereocomplementary Biocatalytic Pathways*.Angewandte Chemie (International ed. in English) · 2021
    Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. An overview of microbial indigo-forming enzymes.Applied microbiology and biotechnology · 2020
    Review
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

4 authors.

Muniba FaizaSchool of Food Science and Engineering, South China University of Technology, Guangzhou, 510640, China.
Shengfeng HuangLaboratory for Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Qingdao, China. hshengf2@mail.sysu.edu.cn.
Dongming LanSchool of Food Science and Engineering, South China University of Technology, Guangzhou, 510640, China.
Yonghua WangSchool of Food Science and Engineering, South China University of Technology, Guangzhou, 510640, China. yonghw@scut.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundUnspecific peroxygenases (UPO) (EC 1.11.2.1) represent an intriguing oxidoreductase sub-subclass of heme proteins with peroxygenase and peroxidase activity. With over 300 identified substrates, UPOs catalyze numerous oxidations including 1- or 2- electron oxygenation, selective oxyfunctionalizations, which make them most significant in organic syntheses and potentially attractive as industrial biocatalysts. There are very few UPOs available with distinct properties, notably, MroUPO which shows behavior ranging between UPO and another heme-thiolate peroxidase, called Chloroperoxidase (CPO). It prompted us to search for more UPOs in fungal kingdom which led us to studying their relationship with CPO.

resultsIn this study, we searched for novel UPOs in more than 800 fungal genomes and found 113 putative UPO-encoding sequences distributed in 35 different fungal species (or strains), amongst which single sequence per species were subjected to phylogeny study along with CPOs. Our phylogenetic study show that the UPOs are distributed in Basidiomycota and Ascomycota phyla of fungi. The sequence analysis helped to classify the UPOs into five distinct subfamilies: classic AaeUPO and four new subfamilies with potential new traits. We have also shown that each of these five subfamilies (supported by) have their own signature motifs. Surprisingly, some of the CPOs appeared to be a type of UPOs indicating that they were previously identified incorrectly. Selection pressure was observed on important motifs in UPOs which could have driven their functional divergence. Furthermore, the sites having different evolutionary rates caused by the functional divergence were also identified on some motifs along with the other relevant amino acid residues. Finally, we predicted critical amino acids responsible for the functional divergence in the UPOs and identified some sequence differences among UPOs, CPOs, and MroUPO to predict it's ranging behavior.

conclusionThis study discovers new UPOs, provides a glimpse of their evolution from CPOs, and presents new insight on their functional divergence. We present a new classification of UPOs and shed new light on its phylogenetics. These different UPOs may exhibit a wide range of characteristics and specificities which may help in various fields of synthetic chemistry and industrial biocatalysts, and may as well lead to an advancement towards the understanding of physiological role of UPOs in fungi.

Indexed as

Evolution, MolecularMultigene FamilyAmino Acid MotifsAmino Acid SequenceAscomycotaBasidiomycotaConserved SequenceGenetic VariationLikelihood FunctionsMixed Function OxygenasesPhylogenySelection, GeneticMixed Function OxygenasesperoxygenaseAgrocybe aegeritaChloroperoxidaseFunctional divergenceFungal genomesPhylogenySelection pressureSubfamiliesSuperfamilyUnspecific peroxygenases

Identifiers

PMID30866798
PMCPMC6417270

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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.