Evidence map›Paper›PMID 29111967›Full record

ArticleMicrobiology (Reading, England)2018

Recombinant expression and characterisation of the oxygen-sensitive 2-enoate reductase from Clostridium sporogenes.

Pawel M Mordaka, Stephen J Hall, Nigel Minton, Gill Stephens

Open access · hybridAbstract read
In one paragraph

Article in Microbiology (Reading, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Pawel M MordakaBioprocess, Environmental and Chemical Technologies Research Group, Faculty of Engineering, University of Nottingham, University Park, Nottingham NG7 2RD, UK.
Stephen J HallBioprocess, Environmental and Chemical Technologies Research Group, Faculty of Engineering, University of Nottingham, University Park, Nottingham NG7 2RD, UK.
Nigel MintonClostridia Research Group, BBSRC/EPSRC Synthetic Biology Research Centre (SBRC), School of Life Sciences, University of Nottingham, University Park, Nottingham NG7 2RD, UK.
Gill StephensBioprocess, Environmental and Chemical Technologies Research Group, Faculty of Engineering, University of Nottingham, University Park, Nottingham NG7 2RD, UK.
University of Nottingham · GBEngineering and Physical Sciences Research Council · GB

Funding

Biotechnology and Biological Sciences Research Council BB/D002826/1Biotechnology and Biological Sciences Research Council BB/G023581/1Biotechnology and Biological Sciences Research Council BB/G023581/2
6 · The paper itself

Abstract

'Ene'-reductases have attracted significant attention for the preparation of chemical intermediates and biologically active products. To date, research has been focussed primarily on Old Yellow Enzyme-like proteins, due to their ease of handling, whereas 2-enoate reductases from clostridia have received much less attention, because of their oxygen sensitivity and a lack of suitable expression systems. A hypothetical 2-enoate reductase gene, fldZ, was identified in Clostridium sporogenes DSM 795. The encoded protein shares a high degree of homology to clostridial FMN- and FAD-dependent 2-enoate reductases, including the cinnamic acid reductase proposed to be involved in amino acid metabolism in proteolytic clostridia. The gene was cloned and overexpressed in Escherichia coli. Successful expression depended on the use of strictly anaerobic conditions for both growth and enzyme preparation, since FldZ was oxygen-sensitive. The enzyme reduced aromatic enoates, such as cinnamic acid or p-coumaric acid, but not short chain unsaturated aliphatic acids. The β,β-disubstituted nitroalkene, (E)-1-nitro-2-phenylpropene, was reduced to enantiopure (R)-1-nitro-2-phenylpropane with a yield of 90 %. By contrast, the α,β-disubstituted nitroalkene, (E)-2-nitro-1-phenylpropene, was reduced with a moderate yield of 56 % and poor enantioselectivity (16 % ee for (S)-2-nitro-1-phenylpropane). The availability of an expression system for this recombinant clostridial 2-enoate reductase will facilitate future characterisation of this unusual class of 'ene'-reductases, and expand the biocatalytic toolbox available for enantioselective hydrogenation of carbon-carbon double bonds.

Indexed as

AnaerobiosisBacterial ProteinsBiocatalysisCloning, MolecularClostridiumEscherichia coliGene ExpressionGenes, BacterialOxidation-ReductionOxidoreductases Acting on CH-CH Group DonorsRecombinant Proteins2-enoate reductaseBacterial ProteinsOxidoreductases Acting on CH-CH Group DonorsRecombinant Proteins2-enoate reductasebioreductionClostridium sporogenes'ene'-reductasehydrogenation of carbon-carbon double bondsnitroalkene reduction

Identifiers

PMID29111967
PMCPMC5882074
OpenAlexW2768068800

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.