# Metabolic engineering of Yarrowia lipolytica for enhanced microbial production of medium-chain α, ω-diols from alkanes via CRISPR-Cas9 mediated pathway optimization and P450 alkane monooxygenase overexpression

**Authors:** Ye Chan Kim, Won Yoon Hwan Choi, Eun-Jung Kim, Byung‐Gee Kim, Hyungdon Yun

PMC · DOI: 10.3389/fbioe.2025.1695661 · Frontiers in Bioengineering and Biotechnology · 2025-10-23

## TL;DR

Scientists engineered a yeast to efficiently convert alkanes into valuable diols, a key step for sustainable chemical production.

## Contribution

First successful microbial production of α, ω-diols from alkanes in yeast using CRISPR-Cas9 and pathway optimization.

## Key findings

- Engineered strain YALI17 produced 1,12-dodecanediol at 0.72 mM from n-dodecane.
- ALK1 overexpression increased production to 1.45 mM, with automated pH control reaching 3.2 mM.
- Yarrowia lipolytica is a promising cell factory for alkane-based biomanufacturing.

## Abstract

Medium- to long-chain α, ω-diols are valuable building blocks for polyesters and polyurethanes, yet their microbial synthesis from inexpensive alkane feedstocks remains largely undeveloped. The oleaginous yeast Yarrowia lipolytica offers advantages over bacterial systems such as Escherichia coli for alkane conversion due to its inherent capacity to metabolize hydrophobic substrates.

To enable de novo α, ω-diol production from alkanes, we used CRISPR-Cas9 to delete ten genes involved in fatty alcohol oxidation (including FADH, ADH1 -8, and FAO1) and four genes linked to fatty aldehyde oxidation (FALDH1 -4). This generated the strain YALI17, with reduced over-oxidation activity. Further metabolic enhancement was achieved by overexpressing alkane hydroxylase genes, particularly ALK1. Fermentation performance was evaluated under controlled pH conditions using n-dodecane as the substrate.

The engineered strain YALI17 produced 1,12-dodecanediol at 0.72 mM from 50 mM n-dodecane –a 14-fold increase relative to the parental strain. ALK1 overexpression in YALI17 further raised production to 1.45 mM, and automated pH-controlled biotransformation achieved 3.2 mM.

This study demonstrates the first successful biotransformation of medium- to long-chain α, ω-diols directly from alkanes in yeast. The rational pathway design and oxidation-pathway blocking highlight Y. lipolytica as a promising cell factory for alkane-based biomanufacturing and lay the groundwork for sustainable production of high-value diol precursors through targeted metabolic engineering.

## Linked entities

- **Genes:** fadH (NADPH dependent 2,4-dienoyl-CoA reductase FadH) [NCBI Gene 886053], ADH1A (alcohol dehydrogenase 1A (class I), alpha polypeptide) [NCBI Gene 124], ADH1B (alcohol dehydrogenase 1B (class I), beta polypeptide) [NCBI Gene 125], ADH1C (alcohol dehydrogenase 1C (class I), gamma polypeptide) [NCBI Gene 126], ADH4 (alcohol dehydrogenase 4 (class II), pi polypeptide) [NCBI Gene 127], ADH5 (alcohol dehydrogenase 5 (class III), chi polypeptide) [NCBI Gene 128], ADH6 (alcohol dehydrogenase 6 (class V)) [NCBI Gene 130], ADH7 (alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide) [NCBI Gene 131], ADHFE1 (alcohol dehydrogenase iron containing 1) [NCBI Gene 137872], FAO1 (uncharacterized protein) [NCBI Gene 4840653], ACVRL1 (activin A receptor like type 1) [NCBI Gene 94]
- **Chemicals:** n-dodecane (PubChem CID 8182), 1,12-dodecanediol (PubChem CID 79758)
- **Species:** Yarrowia lipolytica (taxon 4952), Escherichia coli (taxon 562)

## Full-text entities

- **Chemicals:** fatty alcohol (MESH:D005233), polyurethanes (MESH:D011140), diol (MESH:D011276), polyesters (MESH:D011091), fatty aldehyde (MESH:C001634), alkane (MESH:D000473), n-dodecane (MESH:C007548), 1,12-dodecanediol (-)
- **Species:** Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Escherichia coli (E. coli, species) [taxon 562], Yarrowia lipolytica (species) [taxon 4952]
- **Cell lines:** YALI17 — Homo sapiens (Human), Induced pluripotent stem cell (CVCL_8991)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12588895/full.md

## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC12588895/full.md

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Source: https://tomesphere.com/paper/PMC12588895