Evidence map›Paper›PMID 38683670›Full record

ArticleMicrobial biotechnology2024

Unravelling the role of the group 6 soluble di-iron monooxygenase (SDIMO) SmoABCD in alkane metabolism and chlorinated alkane degradation.

Eleonora Ferrari, Giulio Di Benedetto, Andrea Firrincieli, Alessandro Presentato, Dario Frascari, Martina Cappelletti

Abstract read
In one paragraph

Article in Microbial biotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

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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

6 citing papers in PubMed.

  1. Article
  2. Cell Disruption and RNA Extraction fromInternational journal of molecular sciences · 2026
    Article
  3. Article
  4. Generalization of Classification of AlkB Family Alkane Monooxygenases fromInternational journal of molecular sciences · 2025
    Article
  5. ResistantMicroorganisms · 2024
    Article
  6. 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

6 authors.

Eleonora FerrariDepartment of Pharmacy and Biotechnology (FaBit), University of Bologna, Bologna, Italy.
Giulio Di BenedettoDepartment of Pharmacy and Biotechnology (FaBit), University of Bologna, Bologna, Italy.
Andrea FirrincieliDepartment for Innovation in Biological, Agro-Food and Forest Systems, University of Tuscia, Viterbo, Italy.
Alessandro PresentatoDepartment of Biological, Chemical and Pharmaceutical Sciences and Technologies (STEBICEF), University of Palermo, Palermo, Italy.
Dario FrascariDepartment of Civil, Chemical, Environmental and Materials Engineering (DICAM), University of Bologna, Bologna, Italy.
Martina CappellettiDepartment of Pharmacy and Biotechnology (FaBit), University of Bologna, Bologna, Italy.ORCID 0000-0002-6238-8296

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Soluble di-iron monooxygenases (SDIMOs) are multi-component enzymes catalysing the oxidation of various substrates. These enzymes are characterized by high sequence and functional diversity that is still not well understood despite their key role in biotechnological processes including contaminant biodegradation. In this study, we analysed a mutant of Rhodoccocus aetherivorans BCP1 (BCP1-2.10) characterized by a transposon insertion in the gene smoA encoding the alpha subunit of the plasmid-located SDIMO SmoABCD. The mutant BCP1-2.10 showed a reduced capacity to grow on propane, lost the ability to grow on butane, pentane and n-hexane and was heavily impaired in the capacity to degrade chloroform and trichloroethane. The expression of the additional SDIMO prmABCD in BCP1-2.10 probably allowed the mutant to partially grow on propane and to degrade it, to some extent, together with the other short-chain n-alkanes. The complementation of the mutant, conducted by introducing smoABCD in the genome as a single copy under a constitutive promoter or within a plasmid under a thiostreptone-inducible promoter, allowed the recovery of the alkanotrophic phenotype as well as the capacity to degrade chlorinated n-alkanes. The heterologous expression of smoABCD allowed a non-alkanotrophic Rhodococcus strain to grow on pentane and n-hexane when the gene cluster was introduced together with the downstream genes encoding alcohol and aldehyde dehydrogenases and a GroEL chaperon. BCP1 smoA gene was shown to belong to the group 6 SDIMOs, which is a rare group of monooxygenases mostly present in Mycobacterium genus and in a few Rhodococcus strains. SmoABCD originally evolved in Mycobacterium and was then acquired by Rhodococcus through horizontal gene transfer events. This work extends the knowledge of the biotechnologically relevant SDIMOs by providing functional and evolutionary insights into a group 6 SDIMO in Rhodococcus and demonstrating its key role in the metabolism of short-chain alkanes and degradation of chlorinated n-alkanes.

Indexed as

AlkanesMixed Function OxygenasesBiotransformationDNA Transposable ElementsGenetic Complementation TestHydrocarbons, ChlorinatedMutagenesis, InsertionalAlkanesDNA Transposable ElementsHydrocarbons, ChlorinatedMixed Function Oxygenases

Identifiers

PMID38683670
PMCPMC11057499

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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.