Biocatalytic synthesis of dihydroxy fatty acids as lipid mediators from polyunsaturated fatty acids by double dioxygenation of the microbial 12<i>S‐</i>lipoxygenase

Abstract

Abstract Leukotrienes (LTs) and maresins (MaRs) are human lipid mediators (LMs) involved in immune response and anti‐inflammation, respectively. These compounds and their isomers are generated in trace amounts by lipoxygenases (LOXs) in human macrophages and neutrophils. These LMs have been synthesized using nonenvironmentally benign synthetic protocols, which are expensive. 8 S ‐ and 15 S ‐LOXs with double dioxygenating activities have previously been reported, whereas 12 S‐ LOX with double dioxygenating activity have not been reported to date. Here, we discovered a wild‐type 12 S‐ LOX with double dioxygenating activity from the bacterium Endozoicomonas numazuensis , which produced dihydroxy fatty acids (DiHFAs) as LMs from polyunsaturated fatty acids via double dioxygenation. The enzyme activity for producing DiHFA was approximately 550‐fold higher than that of mammalian LOX with double dioxygenating activity. The microbial 12 S ‐LOX converted 3.00 mM of arachidonic acid, eicosapentaenoic acid, docosapentaenoic acid, and docosahexaenoic acid to 2.37 mM (797 mg/L) 6‐ trans ‐8‐ cis ‐12 S ‐epimer of LTB4, 1.59 mM (532 mg/L) 6‐ trans ‐8‐ cis ‐12 S ‐epimer of LTB5, 1.35 mM (498 mg/L) 10‐ cis ‐12‐ trans ‐7 S ‐epimer of MaR1 n‐3 DPA , and 1.54 mM (555 mg/L) 10‐ cis ‐12‐ trans ‐7 S ‐epimer of MaR1 within 2 h, which were 5.3‐, 7.6‐, 3.1‐, and 5.5‐fold higher than those biosynthesized by the previously reported microbial engineered 12 S ‐LOX with double dioxygenating activity, respectively. These findings contribute to the efficient and environmentally friendly biosynthesis of LMs and stimulate physiological study on LMs.

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