Characterization of 2-phenanthroate:CoA ligase from the sulfate-reducing, phenanthrene-degrading enrichment culture TRIP.
| Autor: | Kaplieva-Dudek I; Environmental Microbiology and Biotechnology (EMB), Aquatic Microbiology, Faculty of Chemistry, University of Duisburg-Essen, Essen, Germany., Samak NA; Environmental Microbiology and Biotechnology (EMB), Aquatic Microbiology, Faculty of Chemistry, University of Duisburg-Essen, Essen, Germany., Bormann J; Department of Chemical Biology, ZMB, Faculty of Biology, University of Duisburg-Essen, Essen, Germany.; Analytics Core Facility Essen, ZMB, Faculty of Biology, University of Duisburg-Essen, Essen, Germany., Kaschani F; Department of Chemical Biology, ZMB, Faculty of Biology, University of Duisburg-Essen, Essen, Germany.; Analytics Core Facility Essen, ZMB, Faculty of Biology, University of Duisburg-Essen, Essen, Germany., Kaiser M; Department of Chemical Biology, ZMB, Faculty of Biology, University of Duisburg-Essen, Essen, Germany., Meckenstock RU; Environmental Microbiology and Biotechnology (EMB), Aquatic Microbiology, Faculty of Chemistry, University of Duisburg-Essen, Essen, Germany. |
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| Jazyk: | angličtina |
| Zdroj: | Applied and environmental microbiology [Appl Environ Microbiol] 2024 Oct 23; Vol. 90 (10), pp. e0129624. Date of Electronic Publication: 2024 Sep 09. |
| DOI: | 10.1128/aem.01296-24 |
| Abstrakt: | Polycyclic aromatic hydrocarbons (PAHs) are chemically stable pollutants that are poorly degraded by microorganisms in anoxic sediments. The anaerobic degradation pathway of PAHs such as phenanthrene starts with a carboxylation reaction forming phenanthroic acid. In this study, we identified and characterized the next enzyme in the pathway, the 2-phenanthroate:CoA ligase involved in the ATP-dependent formation of 2-phenanthroyl-CoA from cell-free extracts of the sulfate-reducing enrichment culture TRIP grown anaerobically with phenanthrene. The identified gene sequence indicated that 2-phenanthroate:CoA ligase belongs to the phenylacetate:CoA ligase-like enzyme family. Based on the sequence, we predict a two-domain structure of the 2-phenanthroate:CoA ligase with a typical large N-terminal and a smaller C-terminal domain. Partial purification of 2-phenanthroate:CoA ligase allowed us to identify the coding gene in the genome. 2-Phenanthroate:CoA ligase gene was heterologously expressed in Escherichia coli . Characterization of the 2-phenanthroate:CoA ligase was performed using the partially purified enzyme from cell-free extract and the purified recombinant enzyme. Testing all possible phenanthroic acid isomers as substrate for the ligase reaction showed that 2-phenanthroic acid is the preferred substrate and only 3-phenanthroic acid can be utilized to a minor extent. This also suggests that the product of the prior carboxylase reaction is 2-phenanthroic acid. 2-Phenanthroate:CoA ligase has an optimal activity at pH 7.5 and is oxygen-insensitive, analogous to other aryl-CoA ligases. In contrast to aryl-Coenzyme A ligases reported in the literature, which need Mg 2+ as cofactor, 2-phenanthroate:CoA ligase showed greatest activity with a combination of 5 mM MgCl Importance: Polycyclic aromatic hydrocarbons (PAHs) constitute a class of very toxic and persistent pollutants in the environment. However, the anaerobic degradation of three-ring PAHs such as phenanthrene is barely investigated. The initial degradation step starts with a carboxylation followed by a CoA‑thioesterification reaction performed by an aryl-CoA ligase. The formation of a CoA-thioester is an important step in the degradation pathway of aromatic compounds because the CoA-ester is needed for all downstream biochemical reactions in the pathway. Furthermore, we provide biochemical proof for the identification of the first genes for anaerobic phenanthrene degradation. Results presented here provide information about the biochemical and structural properties of the purified 2‑phenanthroate:CoA ligase and expand our knowledge of aryl-CoA ligases. Competing Interests: The authors declare no conflict of interest. |
| Databáze: | MEDLINE |
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