High-yield production of vanillin from ferulic acid by a coenzyme-independent decarboxylase/oxygenase two-stage process - PubMed (original) (raw)
. 2015 May 25;32(3):335-9.
doi: 10.1016/j.nbt.2015.03.002. Epub 2015 Mar 9.
Affiliations
- PMID: 25765579
- DOI: 10.1016/j.nbt.2015.03.002
High-yield production of vanillin from ferulic acid by a coenzyme-independent decarboxylase/oxygenase two-stage process
Toshiki Furuya et al. N Biotechnol. 2015.
Abstract
Vanillin is one of the world's most important flavor and fragrance compounds in foods and cosmetics. Recently, we demonstrated that vanillin could be produced from ferulic acid via 4-vinylguaiacol in a coenzyme-independent manner using the decarboxylase Fdc and the oxygenase Cso2. In this study, we investigated a new two-pot bioprocess for vanillin production using the whole-cell catalyst of Escherichia coli expressing Fdc in the first stage and that of E. coli expressing Cso2 in the second stage. We first optimized the second-step Cso2 reaction from 4-vinylguaiacol to vanillin, a rate-determining step for the production of vanillin. Addition of FeCl2 to the cultivation medium enhanced the activity of the resulting E. coli cells expressing Cso2, an iron protein belonging to the carotenoid cleavage oxygenase family. Furthermore, a butyl acetate-water biphasic system was effective in improving the production of vanillin. Under the optimized conditions, we attempted to produce vanillin from ferulic acid by a two-pot bioprocess on a flask scale. In the first stage, E. coli cells expressing Fdc rapidly decarboxylated ferulic acid and completely converted 75 mM of this substrate to 4-vinylguaiacol within 2 h at pH 9.0. After the first-stage reaction, cells were removed from the reaction mixture by centrifugation, and the pH of the resulting supernatant was adjusted to 10.5, the optimal pH for Cso2. This solution was subjected to the second-stage reaction. In the second stage, E. coli cells expressing Cso2 efficiently oxidized 4-vinylguaiacol to vanillin. The concentration of vanillin reached 52 mM (7.8 g L(-1)) in 24 h, which is the highest level attained to date for the biotechnological production of vanillin using recombinant cells.
Copyright © 2015 Elsevier B.V. All rights reserved.
Similar articles
- Biotechnological production of vanillin using immobilized enzymes.
Furuya T, Kuroiwa M, Kino K. Furuya T, et al. J Biotechnol. 2017 Feb 10;243:25-28. doi: 10.1016/j.jbiotec.2016.12.021. Epub 2016 Dec 29. J Biotechnol. 2017. PMID: 28042012 - A coenzyme-independent decarboxylase/oxygenase cascade for the efficient synthesis of vanillin.
Furuya T, Miura M, Kino K. Furuya T, et al. Chembiochem. 2014 Oct 13;15(15):2248-54. doi: 10.1002/cbic.201402215. Epub 2014 Aug 27. Chembiochem. 2014. PMID: 25164030 - Site-directed mutagenesis of coenzyme-independent carotenoid oxygenase CSO2 to enhance the enzymatic synthesis of vanillin.
Yao X, Lv Y, Yu H, Cao H, Wang L, Wen B, Gu T, Wang F, Sun L, Xin F. Yao X, et al. Appl Microbiol Biotechnol. 2020 May;104(9):3897-3907. doi: 10.1007/s00253-020-10433-1. Epub 2020 Mar 4. Appl Microbiol Biotechnol. 2020. PMID: 32130469 - Vanillin biotechnology: the perspectives and future.
Banerjee G, Chattopadhyay P. Banerjee G, et al. J Sci Food Agric. 2019 Jan 30;99(2):499-506. doi: 10.1002/jsfa.9303. Epub 2018 Sep 27. J Sci Food Agric. 2019. PMID: 30094833 Review. - Challenges and advances in biotechnological approaches for the synthesis of canolol and other vinylphenols from biobased p-hydroxycinnamic acids: a review.
Lomascolo A, Odinot E, Villeneuve P, Lecomte J. Lomascolo A, et al. Biotechnol Biofuels Bioprod. 2023 Nov 14;16(1):173. doi: 10.1186/s13068-023-02425-w. Biotechnol Biofuels Bioprod. 2023. PMID: 37964324 Free PMC article. Review.
Cited by
- Engineering a coenzyme-independent dioxygenase for one-step production of vanillin from ferulic acid.
Fujimaki S, Sakamoto S, Shimada S, Kino K, Furuya T. Fujimaki S, et al. Appl Environ Microbiol. 2024 Jun 18;90(6):e0023324. doi: 10.1128/aem.00233-24. Epub 2024 May 10. Appl Environ Microbiol. 2024. PMID: 38727223 Free PMC article. - A comprehensive review of eclectic approaches to the biological synthesis of vanillin and their application towards the food sector.
Venkataraman S, Athilakshmi JK, Rajendran DS, Bharathi P, Kumar VV. Venkataraman S, et al. Food Sci Biotechnol. 2024 Jan 3;33(5):1019-1036. doi: 10.1007/s10068-023-01484-x. eCollection 2024 Apr. Food Sci Biotechnol. 2024. PMID: 38440686 Review. - Nature stays natural: two novel chemo-enzymatic one-pot cascades for the synthesis of fragrance and flavor aldehydes.
Giparakis S, Winkler M, Rudroff F. Giparakis S, et al. Green Chem. 2023 Dec 22;26(3):1338-1344. doi: 10.1039/d3gc04191c. eCollection 2024 Feb 5. Green Chem. 2023. PMID: 38323304 Free PMC article. - Strategies for improving the production of bio-based vanillin.
Liu Y, Sun L, Huo YX, Guo S. Liu Y, et al. Microb Cell Fact. 2023 Aug 5;22(1):147. doi: 10.1186/s12934-023-02144-9. Microb Cell Fact. 2023. PMID: 37543600 Free PMC article. Review. - Rationally Guided Improvement of NOV1 Dioxygenase for the Conversion of Lignin-Derived Isoeugenol to Vanillin.
De Simone M, Alvigini L, Alonso-Cotchico L, Brissos V, Caroli J, Lucas MF, Monza E, Melo EP, Mattevi A, Martins LO. De Simone M, et al. Biochemistry. 2023 Jan 17;62(2):419-428. doi: 10.1021/acs.biochem.2c00168. Epub 2022 Jun 10. Biochemistry. 2023. PMID: 35687874 Free PMC article.