volume 14 issue 6 pages 4130-4138

Biological Reaction Engineering for the Preparation of C9 Chemicals from Oleic Acid: 9-Aminononanoic Acid, 1,9-Nonanediol, 9-Amino-1-nonanol, and 1,9-Diaminononane

Publication typeJournal Article
Publication date2024-03-04
scimago Q1
wos Q1
SJR3.782
CiteScore19.5
Impact factor13.1
ISSN21555435
General Chemistry
Catalysis
Abstract
Engineering of native and recombinant enzyme reactions in whole-cell biocatalysis may allow the production of a variety of chemicals. In particular, fine-tuning of the reaction selectivity may enable the preparation of a desired product to a high conversion. Here, we demonstrated that various C9 chemicals such as 9-aminononanoic acid, 1,9-nonanediol, 9-amino-1-nonanol, and 1,9-diaminononane could be produced from renewable C18 oleic acid. As a representative example, activation of six recombinant enzyme reactions (e.g., fatty acid double bond hydratase, long-chain secondary alcohol dehydrogenase, Baeyer–Villiger monooxygenase, lipase, primary alcohol dehydrogenase, and ω-aminotransferases) with repression of one native enzyme reaction (i.e., aldehyde dehydrogenase) in Escherichia coli-based biocatalysis led to the formation of 9-aminononanoic acid with an isolation yield of 54% from oleic acid via 10-hydroxyoctadecanoic acid, 10-keto-octadecanoic acid, 9-(nonanoyloxy)nonanoic acid, 9-hydroxynonanoic acid, and 9-oxo-nonanoic acid. This study will contribute to biosynthesis of not only ω-aminoalkanoic acids but also ω-amino-1-alkanols and α,ω-diaminoalkanes from renewable fatty acids (e.g., oleic acid and ricinoleic acid).
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Hwang S. et al. Biological Reaction Engineering for the Preparation of C9 Chemicals from Oleic Acid: 9-Aminononanoic Acid, 1,9-Nonanediol, 9-Amino-1-nonanol, and 1,9-Diaminononane // ACS Catalysis. 2024. Vol. 14. No. 6. pp. 4130-4138.
GOST all authors (up to 50) Copy
Hwang S., Woo J., Choi G. E., Choi G., OH D., Seo J., Seo J., Park J. B. Biological Reaction Engineering for the Preparation of C9 Chemicals from Oleic Acid: 9-Aminononanoic Acid, 1,9-Nonanediol, 9-Amino-1-nonanol, and 1,9-Diaminononane // ACS Catalysis. 2024. Vol. 14. No. 6. pp. 4130-4138.
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RIS Copy
TY - JOUR
DO - 10.1021/acscatal.4c00302
UR - https://pubs.acs.org/doi/10.1021/acscatal.4c00302
TI - Biological Reaction Engineering for the Preparation of C9 Chemicals from Oleic Acid: 9-Aminononanoic Acid, 1,9-Nonanediol, 9-Amino-1-nonanol, and 1,9-Diaminononane
T2 - ACS Catalysis
AU - Hwang, Se-Yeun
AU - Woo, Ji-Min
AU - Choi, Go Eun
AU - Choi, Goeun
AU - OH, DEOK-KUN
AU - Seo, Joo-Hyun
AU - Seo, Joohyun
AU - Park, Jin Byung
PY - 2024
DA - 2024/03/04
PB - American Chemical Society (ACS)
SP - 4130-4138
IS - 6
VL - 14
SN - 2155-5435
ER -
BibTex |
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BibTex (up to 50 authors) Copy
@article{2024_Hwang,
author = {Se-Yeun Hwang and Ji-Min Woo and Go Eun Choi and Goeun Choi and DEOK-KUN OH and Joo-Hyun Seo and Joohyun Seo and Jin Byung Park},
title = {Biological Reaction Engineering for the Preparation of C9 Chemicals from Oleic Acid: 9-Aminononanoic Acid, 1,9-Nonanediol, 9-Amino-1-nonanol, and 1,9-Diaminononane},
journal = {ACS Catalysis},
year = {2024},
volume = {14},
publisher = {American Chemical Society (ACS)},
month = {mar},
url = {https://pubs.acs.org/doi/10.1021/acscatal.4c00302},
number = {6},
pages = {4130--4138},
doi = {10.1021/acscatal.4c00302}
}
MLA
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MLA Copy
Hwang, Se-Yeun, et al. “Biological Reaction Engineering for the Preparation of C9 Chemicals from Oleic Acid: 9-Aminononanoic Acid, 1,9-Nonanediol, 9-Amino-1-nonanol, and 1,9-Diaminononane.” ACS Catalysis, vol. 14, no. 6, Mar. 2024, pp. 4130-4138. https://pubs.acs.org/doi/10.1021/acscatal.4c00302.
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