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Bioprospecting for polyesterase activity relevant for PET degradation in marine Enterobacterales isolates

Plastics have quickly become an integral part of modern life. Due to excessive production and improper waste disposal, they are recognized as contaminants present in practically all habitat types. Although there are several polymers, polyethylene terephthalate (PET) is of particular concern due to i...

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Autores principales: Galarza–Verkovitch, Denisse, Turak, Onur, Wiese, Jutta, Rahn, Tanja, Hentschel, Ute, Borchert, Erik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AIMS Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10462454/
https://www.ncbi.nlm.nih.gov/pubmed/37649797
http://dx.doi.org/10.3934/microbiol.2023027
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author Galarza–Verkovitch, Denisse
Turak, Onur
Wiese, Jutta
Rahn, Tanja
Hentschel, Ute
Borchert, Erik
author_facet Galarza–Verkovitch, Denisse
Turak, Onur
Wiese, Jutta
Rahn, Tanja
Hentschel, Ute
Borchert, Erik
author_sort Galarza–Verkovitch, Denisse
collection PubMed
description Plastics have quickly become an integral part of modern life. Due to excessive production and improper waste disposal, they are recognized as contaminants present in practically all habitat types. Although there are several polymers, polyethylene terephthalate (PET) is of particular concern due to its abundance in the environment. There is a need for a solution that is both cost-effective and ecologically friendly to address this pollutant. The use of microbial depolymerizing enzymes could offer a biological avenue for plastic degradation, though the full potential of these enzymes is yet to be uncovered. The purpose of this study was to use (1) plate-based screening methods to investigate the plastic degradation potential of marine bacteria from the order Enterobacterales collected from various organismal and environmental sources, and (2) perform genome-based analysis to identify polyesterases potentially related to PET degradation. 126 bacterial isolates were obtained from the strain collection of RD3, Research Unit Marine Symbioses-GEOMAR-and sequentially tested for esterase and polyesterase activity, in combination here referred to as PETase–like activity. The results show that members of the microbial families Alteromonadaceae, Shewanellaceae, and Vibrionaceae, derived from marine sponges and bryozoans, are the most promising candidates within the order Enterobacterales. Furthermore, 389 putative hydrolases from the α/β superfamily were identified in 23 analyzed genomes, of which 22 were sequenced for this study. Several candidates showed similarities with known PETases, indicating underlying enzymatic potential within the order Enterobacterales for PET degradation.
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spelling pubmed-104624542023-08-30 Bioprospecting for polyesterase activity relevant for PET degradation in marine Enterobacterales isolates Galarza–Verkovitch, Denisse Turak, Onur Wiese, Jutta Rahn, Tanja Hentschel, Ute Borchert, Erik AIMS Microbiol Research Article Plastics have quickly become an integral part of modern life. Due to excessive production and improper waste disposal, they are recognized as contaminants present in practically all habitat types. Although there are several polymers, polyethylene terephthalate (PET) is of particular concern due to its abundance in the environment. There is a need for a solution that is both cost-effective and ecologically friendly to address this pollutant. The use of microbial depolymerizing enzymes could offer a biological avenue for plastic degradation, though the full potential of these enzymes is yet to be uncovered. The purpose of this study was to use (1) plate-based screening methods to investigate the plastic degradation potential of marine bacteria from the order Enterobacterales collected from various organismal and environmental sources, and (2) perform genome-based analysis to identify polyesterases potentially related to PET degradation. 126 bacterial isolates were obtained from the strain collection of RD3, Research Unit Marine Symbioses-GEOMAR-and sequentially tested for esterase and polyesterase activity, in combination here referred to as PETase–like activity. The results show that members of the microbial families Alteromonadaceae, Shewanellaceae, and Vibrionaceae, derived from marine sponges and bryozoans, are the most promising candidates within the order Enterobacterales. Furthermore, 389 putative hydrolases from the α/β superfamily were identified in 23 analyzed genomes, of which 22 were sequenced for this study. Several candidates showed similarities with known PETases, indicating underlying enzymatic potential within the order Enterobacterales for PET degradation. AIMS Press 2023-06-15 /pmc/articles/PMC10462454/ /pubmed/37649797 http://dx.doi.org/10.3934/microbiol.2023027 Text en © 2023 the Author(s), licensee AIMS Press https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) )
spellingShingle Research Article
Galarza–Verkovitch, Denisse
Turak, Onur
Wiese, Jutta
Rahn, Tanja
Hentschel, Ute
Borchert, Erik
Bioprospecting for polyesterase activity relevant for PET degradation in marine Enterobacterales isolates
title Bioprospecting for polyesterase activity relevant for PET degradation in marine Enterobacterales isolates
title_full Bioprospecting for polyesterase activity relevant for PET degradation in marine Enterobacterales isolates
title_fullStr Bioprospecting for polyesterase activity relevant for PET degradation in marine Enterobacterales isolates
title_full_unstemmed Bioprospecting for polyesterase activity relevant for PET degradation in marine Enterobacterales isolates
title_short Bioprospecting for polyesterase activity relevant for PET degradation in marine Enterobacterales isolates
title_sort bioprospecting for polyesterase activity relevant for pet degradation in marine enterobacterales isolates
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10462454/
https://www.ncbi.nlm.nih.gov/pubmed/37649797
http://dx.doi.org/10.3934/microbiol.2023027
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