Evidence map›Paper›PMID 32719558›Full record

ArticleNature chemical biology2020

Enzymatic C-H activation of aromatic compounds through CO

Godwin A Aleku, Annica Saaret, Ruth T Bradshaw-Allen, Sasha R Derrington, Gabriel R Titchiner, Irina Gostimskaya, Deepankar Gahloth, David A Parker, Sam Hay, David Leys

Abstract read
PubMed Publisher
In one paragraph

Article in Nature chemical biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Enzymatic Cascades for Stereoselective and Regioselective Amide Bond Assembly.Angewandte Chemie (International ed. in English) · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Enzymatic Conversion of COChemical reviews · 2023
    Review
  7. EnzymaticACS sustainable chemistry & engineering · 2022
    Article
  8. Immobilization of carbonic anhydrase for COApplied microbiology and biotechnology · 2022
    Review
  9. Article
  10. Article
  11. Review
  12. Structure and Mechanism ofACS catalysis · 2021
    Article
  13. Biocatalytic C-C Bond Formation for One Carbon Resource Utilization.International journal of molecular sciences · 2021
    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

10 authors.

Godwin A AlekuManchester Institute of Biotechnology, Department of Chemistry, University of Manchester, Manchester, UK.
Annica SaaretManchester Institute of Biotechnology, Department of Chemistry, University of Manchester, Manchester, UK.ORCID http://orcid.org/0000-0001-6315-6537
Ruth T Bradshaw-AllenManchester Institute of Biotechnology, Department of Chemistry, University of Manchester, Manchester, UK.
Sasha R DerringtonManchester Institute of Biotechnology, Department of Chemistry, University of Manchester, Manchester, UK.
Gabriel R TitchinerManchester Institute of Biotechnology, Department of Chemistry, University of Manchester, Manchester, UK.
Irina GostimskayaManchester Institute of Biotechnology, Department of Chemistry, University of Manchester, Manchester, UK.ORCID http://orcid.org/0000-0003-0373-6251
Deepankar GahlothManchester Institute of Biotechnology, Department of Chemistry, University of Manchester, Manchester, UK.
David A ParkerInnovation/Biodomain, Shell International Exploration and Production Inc., Westhollow Technology Center, Houston, TX, USA.
Sam HayManchester Institute of Biotechnology, Department of Chemistry, University of Manchester, Manchester, UK.ORCID http://orcid.org/0000-0003-3274-0938
David LeysManchester Institute of Biotechnology, Department of Chemistry, University of Manchester, Manchester, UK. david.leys@manchester.ac.uk.ORCID http://orcid.org/0000-0003-4845-8443

Funding

Biotechnology and Biological Sciences Research Council BB/K017802Biotechnology and Biological Sciences Research Council BB/P000622/1
6 · The paper itself

Abstract

The direct C-H carboxylation of aromatic compounds is an attractive route to the corresponding carboxylic acids, but remains challenging under mild conditions. It has been proposed that the first step in anaerobic microbial degradation of recalcitrant aromatic compounds is a UbiD-mediated carboxylation. In this study, we use the UbiD enzyme ferulic acid decarboxylase (Fdc) in combination with a carboxylic acid reductase to create aromatic degradation-inspired cascade reactions, leading to efficient functionalization of styrene through CO

Indexed as

Amino Acid SequenceBenzofuransBiocatalysisBiodegradation, EnvironmentalCarbon DioxideCarboxylic AcidsCarboxy-LyasesDecarboxylationDrug Evaluation, PreclinicalEnzyme ActivationGenomic LibraryHydrocarbons, AromaticModels, MolecularMolecular StructureMutationNaphthalenes1-naphthoic acid3-octaprenyl-4-hydroxybenzoate carboxy-lyasebenzofuranBenzofuransCarbon Dioxidecarboxylic acid reductaseCarboxylic AcidsCarboxy-LyasesHydrocarbons, AromaticNaphthalenesOxidoreductasesphenylacrylic acid decarboxylaseStyrene

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.