Breeding High-Yield Ethyl Caproate-Producing <i>Saccharomyces cerevisiae</i> in Sake: Flux Regulation from Glycolytic Fermentation to the FAS Pathway and Alcohol Acyltransferase Overexpression

Ethyl caproate is the characteristic aroma compound with an apple-like scent in Ginjoka sake. However, the medium-chain acyl-CoA flux of the fatty acid synthesis (FAS) pathway originating from glycolytic fermentation and the precursor-induced alcohol acyltransferase (AAT) activity by natural yeast limits the ethyl caproate content in sake. Here, we established combinatorial strategies involving genetic engineering and adaptive laboratory evolution (ALE) to increase the ethyl caproate production by <i>Saccharomyces cerevisiae</i>. In this study, we screened <i>Saccharomyces cerevisiae</i> YH-2, which exhibited high ethanol and ester yields , achieving a trade-off between FAS flux and energy metabolism. Subsequently, the cerulenin-resistant mutant strain YH-2-34, after 15 passages of adaptive domestication, produced 4.13 times more caproic acid than the wild type. This increase is attributed to the G1250S variation in the <i>FAS2</i> sequences, which mediate acyl-CoA chain length in the FAS pathway, thereby producing more caproyl-CoA as the precursor. While AAT activity increased 2.40 times in the mutant YH-2-34, both <i>EEB1</i> and <i>EHT1</i> genes, which together encode AAT responsible for esterifying ethyl caproate, played critical roles. Although <i>pEEB1s</i> overexpression affected cell viability and ethyl caproate production, <i>pEHT1s</i> overexpression successfully increased the yield of ethyl caproate during post-fermentation. Finally, the yield of YH-2-34 with <i>EHT1</i> overexpression achieved a significant increase from 1.21 to 7.40 mg/L in sake fermentation. By regulating the flux from glycolytic fermentation to the FAS pathway and overexpressing AAT, we constructed a high-yield ethyl-caproate-producing <i>Saccharomyces cerevisiae</i> strain. This may bring practical transformations to traditional brewing industries.

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Publication Details

Journal
Journal of Agricultural and Food Chemistry
Published
2025-03-19
DOI
https://doi.org/10.1021/acs.jafc.4c11395
Citations
5
Primary Topic
Fermentation and Sensory Analysis
Type
article
Field-Weighted Citation Impact
5.81

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article

Breeding High-Yield Ethyl Caproate-Producing Saccharomyces cerevisiae in Sake: Flux Regulation from Glycolytic Fermentation to the FAS Pathway and Alcohol Acyltransferase Overexpression

Haile Ma, Ronghai He, Rong Zhang, Jing Hao et al.
5 citations
Journal of Agricultural and Food Chemistry
Fermentation and Sensory Analysis
5.81
article

Breeding High-Yield Ethyl Caproate-Producing Saccharomyces cerevisiae in Sake: Flux Regulation from Glycolytic Fermentation to the FAS Pathway and Alcohol Acyltransferase Overexpression

Haile Ma, Ronghai He, Rong Zhang, Jing Hao, Mengyuan Yang
article en
5 citations

Abstract

Ethyl caproate is the characteristic aroma compound with an apple-like scent in Ginjoka sake. However, the medium-chain acyl-CoA flux of the fatty acid synthesis (FAS) pathway originating from glycolytic fermentation and the precursor-induced alcohol acyltransferase (AAT) activity by natural yeast limits the ethyl caproate content in sake. Here, we established combinatorial strategies involving genetic engineering and adaptive laboratory evolution (ALE) to increase the ethyl caproate production by <i>Saccharomyces cerevisiae</i>. In this study, we screened <i>Saccharomyces cerevisiae</i> YH-2, which exhibited high ethanol and ester yields , achieving a trade-off between FAS flux and energy metabolism. Subsequently, the cerulenin-resistant mutant strain YH-2-34, after 15 passages of adaptive domestication, produced 4.13 times more caproic acid than the wild type. This increase is attributed to the G1250S variation in the <i>FAS2</i> sequences, which mediate acyl-CoA chain length in the FAS pathway, thereby producing more caproyl-CoA as the precursor. While AAT activity increased 2.40 times in the mutant YH-2-34, both <i>EEB1</i> and <i>EHT1</i> genes, which together encode AAT responsible for esterifying ethyl caproate, played critical roles. Although <i>pEEB1s</i> overexpression affected cell viability and ethyl caproate production, <i>pEHT1s</i> overexpression successfully increased the yield of ethyl caproate during post-fermentation. Finally, the yield of YH-2-34 with <i>EHT1</i> overexpression achieved a significant increase from 1.21 to 7.40 mg/L in sake fermentation. By regulating the flux from glycolytic fermentation to the FAS pathway and overexpressing AAT, we constructed a high-yield ethyl-caproate-producing <i>Saccharomyces cerevisiae</i> strain. This may bring practical transformations to traditional brewing industries.

Journal of Agricultural and Food ChemistryVol. 73(13)
Jiangsu University (CN)
National Natural Science Foundation of China, Jiangsu Provincial Key Research and Development Program, Senior Talent Foundation of Jiangsu University
Zero hunger
Openalex Percentile: Top 5%
Fermentation and Sensory Analysis
5.81
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