Evidence map›Paper›PMID 10715003›Full record

ArticleJournal of bacteriology2000

Characterization of the gene cluster involved in isoprene metabolism in Rhodococcus sp. strain AD45.

J E van Hylckama Vlieg, H Leemhuis, J H Spelberg, D B Janssen

Open access · greenAbstract read
In one paragraph

Article in Journal of bacteriology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

43 citing papers in PubMed, 95 citations in OpenAlex.

  1. Article
  2. Aerobic catabolism of isobutylene byApplied and environmental microbiology · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Analysis of Essential Isoprene Metabolic Pathway Proteins inApplied and environmental microbiology · 2023
    Article
  9. Article
  10. Article
  11. Article
  12. Microbial oxidation of atmospheric trace gases.Nature reviews. Microbiology · 2022
    Review
  13. Purification and Characterization of the Isoprene Monooxygenase fromApplied and environmental microbiology · 2022
    Article
  14. Article
  15. Article
  16. Characterization of the GlutathioneMicrobiology spectrum · 2021
    Article
  17. Synthetic Biology Approaches to Hydrocarbon Biosensors: A Review.Frontiers in bioengineering and biotechnology · 2021
    Review
  18. Microorganisms · 2020
    Article
  19. Article
  20. 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 at 1 institution in 1 country.

J E van Hylckama VliegDepartment of Biochemistry, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, NL-9747 AG Groningen, The Netherlands.
H Leemhuis
J H Spelberg
D B Janssen
University of Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The genes involved in isoprene (2-methyl-1,3-butadiene) utilization in Rhodococcus sp. strain AD45 were cloned and characterized. Sequence analysis of an 8.5-kb DNA fragment showed the presence of 10 genes of which 2 encoded enzymes which were previously found to be involved in isoprene degradation: a glutathione S-transferase with activity towards 1,2-epoxy-2-methyl-3-butene (isoI) and a 1-hydroxy-2-glutathionyl-2-methyl-3-butene dehydrogenase (isoH). Furthermore, a gene encoding a second glutathione S-transferase was identified (isoJ). The isoJ gene was overexpressed in Escherichia coli and was found to have activity with 1-chloro-2,4-dinitrobenzene and 3,4-dichloro-1-nitrobenzene but not with 1, 2-epoxy-2-methyl-3-butene. Downstream of isoJ, six genes (isoABCDEF) were found; these genes encoded a putative alkene monooxygenase that showed high similarity to components of the alkene monooxygenase from Xanthobacter sp. strain Py2 and other multicomponent monooxygenases. The deduced amino acid sequence encoded by an additional gene (isoG) showed significant similarity with that of alpha-methylacyl-coenzyme A racemase. The results are in agreement with a catabolic route for isoprene involving epoxidation by a monooxygenase, conjugation to glutathione, and oxidation of the hydroxyl group to a carboxylate. Metabolism may proceed by fatty acid oxidation after removal of glutathione by a still-unknown mechanism.

Indexed as

Genes, BacterialHemiterpenesPentanesAlkenesBacterial ProteinsButadienesCloning, MolecularDinitrochlorobenzeneEpoxy CompoundsGene DosageGene ExpressionGlutathione TransferaseMolecular Sequence DataMultigene FamilyNitrobenzenesOpen Reading Frames1,2-dichloro-4-nitrobenzene1-hydroxy-2-glutathionyl-2-methyl-3-butene dehydrogenasealkene monooxygenaseAlkenesalpha-methylacyl-CoA racemaseBacterial ProteinsButadienesDinitrochlorobenzeneEpoxy CompoundsGlutathione TransferaseHemiterpenesisopreneNitrobenzenesOxidoreductasesOxygenasesPentanespropyleneRacemases and EpimerasesRecombinant Proteins

Identifiers

PMID10715003
PMCPMC101893
OpenAlexW2149820431

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.