Evidence map›Paper›PMID 40235172›Full record

ArticleBiotechnology and bioengineering2025

Efficient One-Step Production of 7S,17S- and 10S,17S-Dihydroxydocosahexaenoic Acids by a Double-Oxygenating 15S-Lipoxygenase From Chlamydomonas incerta.

Hyun-Ah Park, Jin Lee, Deok-Kun Oh

Abstract read
In one paragraph

Article in Biotechnology and bioengineering, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Hyun-Ah ParkDepartment of Bioscience and Biotechnology, Konkuk University, Seoul, Republic of Korea.
Jin LeeDepartment of Bioscience and Biotechnology, Konkuk University, Seoul, Republic of Korea.
Deok-Kun OhDepartment of Bioscience and Biotechnology, Konkuk University, Seoul, Republic of Korea.ORCID 0000-0002-6886-7589

Funding

This study was supported by the Mid-Career Researcher Program through the National Research Foundation grant (Grant No. RS-2024-00340835) funded by the Ministry of Science and ICT and the Korea Institute of Planning and Evaluation for Technology in Food, Agriculture, and Forestry (Grant No. RS-2024-00398879) of the Ministry of Agriculture, Food, and Rural Affairs, Republic of Korea. This paper resulted from the Konkuk University research support program in 2024.
6 · The paper itself

Abstract

Specialized pro-resolving mediators (SPMs), such as resolvin D5 (7S,17S-dihydroxydocosahexaenoic acid, 7S,17S-DiHDHA; RvD5) and protectin DX (10S,17S-DiHDHA; PDX), are critical in resolving inflammation in humans. In this study, a unique double-oxygenating 15S-lipoxygenase (15S-LOX) from the alga Chlamydomonas incerta was identified and characterized for its ability to simultaneously produce RvD5 and PDX from docosahexaenoic acid (DHA). Recombinant Escherichia coli expressing the C. incerta 15S-LOX demonstrated enhanced RvD5 and PDX production under the following optimized reaction conditions: pH 8.0, 25°C, 0.5 g dry cells/L, 7.0 mM DHA, 2.0% (w/v) PVP, 2.0% (v/v) DMSO, and 200 mM cysteine used as a reductant. This one-step biocatalytic process produced 2.91 mM (1.05 g/L) RvD5 and 2.18 mM (0.78 g/L) PDX in 90 min, with a total of 5.09 mM (1.83 g/L) and a total conversion yield of 79.6% (w/w). Compared to previously reported two-step biocatalytic processes, this one-step process significantly enhanced the production of particular PDX with improved productivity and simplicity. Structural analysis identified residues Phe667, Ile705, and Leu713 as regioselectivity modulators for the second oxygenation step. This study demonstrates the efficiency and industrial potential of the double-oxygenating LOX as a biocatalyst for simultaneously producing RvD5 and PDX.

Indexed as

Arachidonate 15-LipoxygenaseChlamydomonasDocosahexaenoic AcidsEscherichia coliRecombinant ProteinsArachidonate 15-LipoxygenaseDocosahexaenoic AcidsRecombinant Proteinsarachidonate 15S‐lipoxygenaseChlamydomonas incertadihydroxy fatty acidsprotectin DXresolvin D5

Identifiers

PMID40235172
PMCPMC12152530

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.