Cargando…

Bioconversion of Terephthalic Acid and Ethylene Glycol Into Bacterial Cellulose by Komagataeibacter xylinus DSM 2004 and DSM 46604

Komagataeibacter xylinus strains DSM 2004 and DSM 46604 were evaluated for their ability to grow and produce bacterial cellulose (BC) upon cultivation on terephthalic acid (TA) and ethylene glycol (EG), which are monomers of the petrochemical-derived plastic polyethylene terephthalate (PET). Both st...

Descripción completa

Detalles Bibliográficos
Autores principales: Esmail, Asiyah, Rebocho, Ana T., Marques, Ana C., Silvestre, Sara, Gonçalves, Alexandra, Fortunato, Elvira, Torres, Cristiana A. V., Reis, Maria A. M., Freitas, Filomena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036990/
https://www.ncbi.nlm.nih.gov/pubmed/35480983
http://dx.doi.org/10.3389/fbioe.2022.853322
_version_ 1784693633776091136
author Esmail, Asiyah
Rebocho, Ana T.
Marques, Ana C.
Silvestre, Sara
Gonçalves, Alexandra
Fortunato, Elvira
Torres, Cristiana A. V.
Reis, Maria A. M.
Freitas, Filomena
author_facet Esmail, Asiyah
Rebocho, Ana T.
Marques, Ana C.
Silvestre, Sara
Gonçalves, Alexandra
Fortunato, Elvira
Torres, Cristiana A. V.
Reis, Maria A. M.
Freitas, Filomena
author_sort Esmail, Asiyah
collection PubMed
description Komagataeibacter xylinus strains DSM 2004 and DSM 46604 were evaluated for their ability to grow and produce bacterial cellulose (BC) upon cultivation on terephthalic acid (TA) and ethylene glycol (EG), which are monomers of the petrochemical-derived plastic polyethylene terephthalate (PET). Both strains were able to utilize TA, EG, and their mixtures for BC synthesis, with different performances. K. xylinus DSM 2004 achieved higher BC production from TA (0.81 ± 0.01 g/L), EG (0.64 ± 0.02 g/L), and TA + EG mixtures (0.6 ± 0.1 g/L) than strain DSM 46604. The latter was unable to utilize EG as the sole carbon source and reached a BC production of 0.16 ± 0.01 g/L and 0.23 ± 0.1 g/L from TA alone or TA + EG mixtures, respectively. Further supplementing the media with glucose enhanced BC production by both strains. During cultivation on media containing TA and EG, rapid pH drop due to metabolization of EG into acidic compounds led to some precipitation of TA that was impregnated into the BC pellicles. An adaptation of the downstream procedure involving BC dissolution in NaOH was used for the recovery of pure BC. The different medium composition tested, as well as the downstream procedure, impacted the BC pellicles’ physical properties. Although no variation in terms of the chemical structure were observed, differences in crystallinity degree and microstructure of the produced BC were observed. The BC produced by K. xylinus DSM 2004 had a higher crystallinity (19–64%) than that of the strain DSM 46604 (17–53%). Moreover, the scanning electron microscopy analysis showed a higher fiber diameter for K. xylinus DSM 2004 BC (46–56 nm) than for K. xylinus DSM 46604 (37–49 nm). Dissolution of BC in NaOH did not influence the chemical structure; however, it led to BC conversion from type I to type II, as well as a decrease in crystallinity. These results demonstrate that PET monomers, TA and EG, can be upcycled into a value-added product, BC, presenting an approach that will contribute to lessening the environmental burden caused by plastic disposal in the environment.
format Online
Article
Text
id pubmed-9036990
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-90369902022-04-26 Bioconversion of Terephthalic Acid and Ethylene Glycol Into Bacterial Cellulose by Komagataeibacter xylinus DSM 2004 and DSM 46604 Esmail, Asiyah Rebocho, Ana T. Marques, Ana C. Silvestre, Sara Gonçalves, Alexandra Fortunato, Elvira Torres, Cristiana A. V. Reis, Maria A. M. Freitas, Filomena Front Bioeng Biotechnol Bioengineering and Biotechnology Komagataeibacter xylinus strains DSM 2004 and DSM 46604 were evaluated for their ability to grow and produce bacterial cellulose (BC) upon cultivation on terephthalic acid (TA) and ethylene glycol (EG), which are monomers of the petrochemical-derived plastic polyethylene terephthalate (PET). Both strains were able to utilize TA, EG, and their mixtures for BC synthesis, with different performances. K. xylinus DSM 2004 achieved higher BC production from TA (0.81 ± 0.01 g/L), EG (0.64 ± 0.02 g/L), and TA + EG mixtures (0.6 ± 0.1 g/L) than strain DSM 46604. The latter was unable to utilize EG as the sole carbon source and reached a BC production of 0.16 ± 0.01 g/L and 0.23 ± 0.1 g/L from TA alone or TA + EG mixtures, respectively. Further supplementing the media with glucose enhanced BC production by both strains. During cultivation on media containing TA and EG, rapid pH drop due to metabolization of EG into acidic compounds led to some precipitation of TA that was impregnated into the BC pellicles. An adaptation of the downstream procedure involving BC dissolution in NaOH was used for the recovery of pure BC. The different medium composition tested, as well as the downstream procedure, impacted the BC pellicles’ physical properties. Although no variation in terms of the chemical structure were observed, differences in crystallinity degree and microstructure of the produced BC were observed. The BC produced by K. xylinus DSM 2004 had a higher crystallinity (19–64%) than that of the strain DSM 46604 (17–53%). Moreover, the scanning electron microscopy analysis showed a higher fiber diameter for K. xylinus DSM 2004 BC (46–56 nm) than for K. xylinus DSM 46604 (37–49 nm). Dissolution of BC in NaOH did not influence the chemical structure; however, it led to BC conversion from type I to type II, as well as a decrease in crystallinity. These results demonstrate that PET monomers, TA and EG, can be upcycled into a value-added product, BC, presenting an approach that will contribute to lessening the environmental burden caused by plastic disposal in the environment. Frontiers Media S.A. 2022-04-05 /pmc/articles/PMC9036990/ /pubmed/35480983 http://dx.doi.org/10.3389/fbioe.2022.853322 Text en Copyright © 2022 Esmail, Rebocho, Marques, Silvestre, Gonçalves, Fortunato, Torres, Reis and Freitas. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Esmail, Asiyah
Rebocho, Ana T.
Marques, Ana C.
Silvestre, Sara
Gonçalves, Alexandra
Fortunato, Elvira
Torres, Cristiana A. V.
Reis, Maria A. M.
Freitas, Filomena
Bioconversion of Terephthalic Acid and Ethylene Glycol Into Bacterial Cellulose by Komagataeibacter xylinus DSM 2004 and DSM 46604
title Bioconversion of Terephthalic Acid and Ethylene Glycol Into Bacterial Cellulose by Komagataeibacter xylinus DSM 2004 and DSM 46604
title_full Bioconversion of Terephthalic Acid and Ethylene Glycol Into Bacterial Cellulose by Komagataeibacter xylinus DSM 2004 and DSM 46604
title_fullStr Bioconversion of Terephthalic Acid and Ethylene Glycol Into Bacterial Cellulose by Komagataeibacter xylinus DSM 2004 and DSM 46604
title_full_unstemmed Bioconversion of Terephthalic Acid and Ethylene Glycol Into Bacterial Cellulose by Komagataeibacter xylinus DSM 2004 and DSM 46604
title_short Bioconversion of Terephthalic Acid and Ethylene Glycol Into Bacterial Cellulose by Komagataeibacter xylinus DSM 2004 and DSM 46604
title_sort bioconversion of terephthalic acid and ethylene glycol into bacterial cellulose by komagataeibacter xylinus dsm 2004 and dsm 46604
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036990/
https://www.ncbi.nlm.nih.gov/pubmed/35480983
http://dx.doi.org/10.3389/fbioe.2022.853322
work_keys_str_mv AT esmailasiyah bioconversionofterephthalicacidandethyleneglycolintobacterialcellulosebykomagataeibacterxylinusdsm2004anddsm46604
AT rebochoanat bioconversionofterephthalicacidandethyleneglycolintobacterialcellulosebykomagataeibacterxylinusdsm2004anddsm46604
AT marquesanac bioconversionofterephthalicacidandethyleneglycolintobacterialcellulosebykomagataeibacterxylinusdsm2004anddsm46604
AT silvestresara bioconversionofterephthalicacidandethyleneglycolintobacterialcellulosebykomagataeibacterxylinusdsm2004anddsm46604
AT goncalvesalexandra bioconversionofterephthalicacidandethyleneglycolintobacterialcellulosebykomagataeibacterxylinusdsm2004anddsm46604
AT fortunatoelvira bioconversionofterephthalicacidandethyleneglycolintobacterialcellulosebykomagataeibacterxylinusdsm2004anddsm46604
AT torrescristianaav bioconversionofterephthalicacidandethyleneglycolintobacterialcellulosebykomagataeibacterxylinusdsm2004anddsm46604
AT reismariaam bioconversionofterephthalicacidandethyleneglycolintobacterialcellulosebykomagataeibacterxylinusdsm2004anddsm46604
AT freitasfilomena bioconversionofterephthalicacidandethyleneglycolintobacterialcellulosebykomagataeibacterxylinusdsm2004anddsm46604