Issue 11, 2019

Enzymatic synthesis of new hepoxilins and trioxilins from polyunsaturated fatty acids

Abstract

Hepoxilins (HXs) and trioxilins (TrXs) are lipid mediators that regulate diverse physiological processes at trace amounts in humans. They have been synthesized by chemical methods, which have disadvantages such as low yield, byproduct formation, and use of toxic chemical reagents. Here, we reported the identification of ten types of HXs and TrXs synthesized by recombinant Escherichia coli expressing bacterial arachidonate 15-lipoxygenase and/or epoxide hydrolase using five polyunsaturated fatty acids (PUFAs). Of these, eight types were new. The discovery was due to the microbial enzymes with high activities for the same catalytic activities as those of human enzymes. We succeeded in the efficient, cost-effective, and environmentally friendly biotransformation of PUFAs into nine types of HXs and TrXs by cells, yielding >10 g L−1 of 14,15-HXB3 and 13,14,15-TrXB3, with conversion yields of >70%. Our study contributes to the environmentally friendly synthesis of medicinally important lipid mediators.

Graphical abstract: Enzymatic synthesis of new hepoxilins and trioxilins from polyunsaturated fatty acids

Supplementary files

Article information

Article type
Paper
Submitted
28 Mar 2019
Accepted
30 Apr 2019
First published
01 May 2019

Green Chem., 2019,21, 3172-3181

Enzymatic synthesis of new hepoxilins and trioxilins from polyunsaturated fatty acids

I. Lee, J. An, Y. Ko, J. Park and D. Oh, Green Chem., 2019, 21, 3172 DOI: 10.1039/C9GC01031A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements