Evidence map›Paper›PMID 40323932›Full record

ArticlePloS one2025

Investigating the quaternary structure of a homomultimeric catechol 1,2-dioxygenase: An integrative structural biology study.

Arisbeth Guadalupe Almeida-Juarez, Shirish Chodankar, Liliana Pardo-López, Guadalupe Zavala-Padilla, Enrique Rudiño-Piñera

Abstract read
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Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Arisbeth Guadalupe Almeida-JuarezLaboratorio de Bioquímica Estructural, Departamento de Medicina Molecular y Bioprocesos, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Cuernavaca, Morelos, México.
Shirish ChodankarNational Synchrotron Light Source II, Brookhaven National Laboratory, Upton, New York, United States of America.
Liliana Pardo-LópezLaboratorio de Biotecnología Marina, Departamento de Microbiología Molecular, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Cuernavaca, Morelos, México.
Guadalupe Zavala-PadillaUnidad de Microscopía Electrónica, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Cuernavaca, Morelos, México.
Enrique Rudiño-PiñeraLaboratorio de Bioquímica Estructural, Departamento de Medicina Molecular y Bioprocesos, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Cuernavaca, Morelos, México.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The structural analysis of catechol 1,2 dioxygenase from Stutzerimonas frequens GOM2, SfC12DO, was conducted using various structural techniques. SEC-SAXS experiments revealed that SfC12DO, after lyophilization and reconstitution processes, can form multiple enzymatically active oligomers, including dimers, tetramers, and octamers. These findings differ from previous studies, which reported active dimers in homologous counterparts with available crystallographic structures, or trimers observed exclusively in solution for SfC12DO and its homologous isoA C12DO from Acinetobacter radioresistens under low ionic strength conditions. In some cases, tetramers were also reported, such as for the Rodococcus erythropolis C12DO. The combined results of Small-Angle X-ray Scattering, Dynamic Light Scattering, and Transmission Electron Microscopy experiments provided additional insights into these active oligomers' shape and molecular organization in an aqueous solution. These results highlight the oligomeric structural plasticity of SfC12DO, proving that it can exist in different oligomeric forms depending on the physicochemical characteristics of the solutions in which the experiments were performed. Remarkably, regardless of its oligomeric state, SfC12DO maintains its enzymatic activity even after prior lyophilization. All these characteristics make SfC12DO a putative candidate for bioremediation applications in polluted soils or waters.

Indexed as

Bacterial ProteinsCatechol 1,2-DioxygenaseAcinetobacterModels, MolecularProtein MultimerizationProtein Structure, QuaternaryScattering, Small AngleX-Ray DiffractionBacterial ProteinsCatechol 1,2-Dioxygenase

Identifiers

PMID40323932
PMCPMC12052123

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