Cargando…

Transcriptome analysis and cytochrome P450 monooxygenase reveal the molecular mechanism of Bisphenol A degradation by Pseudomonas putida strain YC-AE1

BACKGROUND: Bisphenol A (BPA) is a rapid spreading organic pollutant that widely used in many industries especially as a plasticizer in polycarbonate plastic and epoxy resins. BPA reported as a prominent endocrine disruptor compound that possesses estrogenic activity and fulminant toxicity. Pseudomo...

Descripción completa

Detalles Bibliográficos
Autores principales: Eltoukhy, Adel, Jia, Yang, Lamraoui, Imane, Abo-Kadoum, M. A., Atta, Omar Mohammad, Nahurira, Ruth, Wang, Junhuan, Yan, Yanchun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9733184/
https://www.ncbi.nlm.nih.gov/pubmed/36482332
http://dx.doi.org/10.1186/s12866-022-02689-6
_version_ 1784846309091442688
author Eltoukhy, Adel
Jia, Yang
Lamraoui, Imane
Abo-Kadoum, M. A.
Atta, Omar Mohammad
Nahurira, Ruth
Wang, Junhuan
Yan, Yanchun
author_facet Eltoukhy, Adel
Jia, Yang
Lamraoui, Imane
Abo-Kadoum, M. A.
Atta, Omar Mohammad
Nahurira, Ruth
Wang, Junhuan
Yan, Yanchun
author_sort Eltoukhy, Adel
collection PubMed
description BACKGROUND: Bisphenol A (BPA) is a rapid spreading organic pollutant that widely used in many industries especially as a plasticizer in polycarbonate plastic and epoxy resins. BPA reported as a prominent endocrine disruptor compound that possesses estrogenic activity and fulminant toxicity. Pseudomonas putida YC-AE1 was isolated in our previous study and exerted a strong degradation capacity toward BPA at high concentrations; however, the molecular degradation mechanism is still enigmatic. RESULTS: We employed RNA sequencing to analyze the differentially expressed genes (DEGs) in the YC-AE1 strain upon BPA induction. Out of 1229 differentially expressed genes, 725 genes were positively regulated, and 504 genes were down-regulated. The pathways of microbial metabolism in diverse environments were significantly enriched among DEGs based on KEGG enrichment analysis. qRT-PCR confirm the involvement of BPA degradation relevant genes in accordance with RNA Seq data. The degradation pathway of BPA in YC-AE1 was proposed with specific enzymes and encoded genes. The role of cytochrome P450 (CYP450) in BPA degradation was further verified. Sever decrease in BPA degradation was recorded by YC-AE1 in the presence of CYP450 inhibitor. Subsequently, CYP450bisdB deficient YC-AE1 strain △ bisdB lost its ability toward BPA transformation comparing with the wild type. Furthermore, Transformation of E. coli with pET-32a-bisdAB empowers it to degrade 66 mg l(−1) of BPA after 24 h. Altogether, the results showed the role of CYP450 in biodegradation of BPA by YC-AE1. CONCLUSION: In this study we propose the molecular basis and the potential role of YC-AE1cytochrome P450 monooxygenase in BPA catabolism. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-022-02689-6.
format Online
Article
Text
id pubmed-9733184
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-97331842022-12-10 Transcriptome analysis and cytochrome P450 monooxygenase reveal the molecular mechanism of Bisphenol A degradation by Pseudomonas putida strain YC-AE1 Eltoukhy, Adel Jia, Yang Lamraoui, Imane Abo-Kadoum, M. A. Atta, Omar Mohammad Nahurira, Ruth Wang, Junhuan Yan, Yanchun BMC Microbiol Research BACKGROUND: Bisphenol A (BPA) is a rapid spreading organic pollutant that widely used in many industries especially as a plasticizer in polycarbonate plastic and epoxy resins. BPA reported as a prominent endocrine disruptor compound that possesses estrogenic activity and fulminant toxicity. Pseudomonas putida YC-AE1 was isolated in our previous study and exerted a strong degradation capacity toward BPA at high concentrations; however, the molecular degradation mechanism is still enigmatic. RESULTS: We employed RNA sequencing to analyze the differentially expressed genes (DEGs) in the YC-AE1 strain upon BPA induction. Out of 1229 differentially expressed genes, 725 genes were positively regulated, and 504 genes were down-regulated. The pathways of microbial metabolism in diverse environments were significantly enriched among DEGs based on KEGG enrichment analysis. qRT-PCR confirm the involvement of BPA degradation relevant genes in accordance with RNA Seq data. The degradation pathway of BPA in YC-AE1 was proposed with specific enzymes and encoded genes. The role of cytochrome P450 (CYP450) in BPA degradation was further verified. Sever decrease in BPA degradation was recorded by YC-AE1 in the presence of CYP450 inhibitor. Subsequently, CYP450bisdB deficient YC-AE1 strain △ bisdB lost its ability toward BPA transformation comparing with the wild type. Furthermore, Transformation of E. coli with pET-32a-bisdAB empowers it to degrade 66 mg l(−1) of BPA after 24 h. Altogether, the results showed the role of CYP450 in biodegradation of BPA by YC-AE1. CONCLUSION: In this study we propose the molecular basis and the potential role of YC-AE1cytochrome P450 monooxygenase in BPA catabolism. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-022-02689-6. BioMed Central 2022-12-09 /pmc/articles/PMC9733184/ /pubmed/36482332 http://dx.doi.org/10.1186/s12866-022-02689-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Eltoukhy, Adel
Jia, Yang
Lamraoui, Imane
Abo-Kadoum, M. A.
Atta, Omar Mohammad
Nahurira, Ruth
Wang, Junhuan
Yan, Yanchun
Transcriptome analysis and cytochrome P450 monooxygenase reveal the molecular mechanism of Bisphenol A degradation by Pseudomonas putida strain YC-AE1
title Transcriptome analysis and cytochrome P450 monooxygenase reveal the molecular mechanism of Bisphenol A degradation by Pseudomonas putida strain YC-AE1
title_full Transcriptome analysis and cytochrome P450 monooxygenase reveal the molecular mechanism of Bisphenol A degradation by Pseudomonas putida strain YC-AE1
title_fullStr Transcriptome analysis and cytochrome P450 monooxygenase reveal the molecular mechanism of Bisphenol A degradation by Pseudomonas putida strain YC-AE1
title_full_unstemmed Transcriptome analysis and cytochrome P450 monooxygenase reveal the molecular mechanism of Bisphenol A degradation by Pseudomonas putida strain YC-AE1
title_short Transcriptome analysis and cytochrome P450 monooxygenase reveal the molecular mechanism of Bisphenol A degradation by Pseudomonas putida strain YC-AE1
title_sort transcriptome analysis and cytochrome p450 monooxygenase reveal the molecular mechanism of bisphenol a degradation by pseudomonas putida strain yc-ae1
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9733184/
https://www.ncbi.nlm.nih.gov/pubmed/36482332
http://dx.doi.org/10.1186/s12866-022-02689-6
work_keys_str_mv AT eltoukhyadel transcriptomeanalysisandcytochromep450monooxygenaserevealthemolecularmechanismofbisphenoladegradationbypseudomonasputidastrainycae1
AT jiayang transcriptomeanalysisandcytochromep450monooxygenaserevealthemolecularmechanismofbisphenoladegradationbypseudomonasputidastrainycae1
AT lamraouiimane transcriptomeanalysisandcytochromep450monooxygenaserevealthemolecularmechanismofbisphenoladegradationbypseudomonasputidastrainycae1
AT abokadoumma transcriptomeanalysisandcytochromep450monooxygenaserevealthemolecularmechanismofbisphenoladegradationbypseudomonasputidastrainycae1
AT attaomarmohammad transcriptomeanalysisandcytochromep450monooxygenaserevealthemolecularmechanismofbisphenoladegradationbypseudomonasputidastrainycae1
AT nahuriraruth transcriptomeanalysisandcytochromep450monooxygenaserevealthemolecularmechanismofbisphenoladegradationbypseudomonasputidastrainycae1
AT wangjunhuan transcriptomeanalysisandcytochromep450monooxygenaserevealthemolecularmechanismofbisphenoladegradationbypseudomonasputidastrainycae1
AT yanyanchun transcriptomeanalysisandcytochromep450monooxygenaserevealthemolecularmechanismofbisphenoladegradationbypseudomonasputidastrainycae1