Hydrogen supplementation improves glucose-based n-caproate production in Caproiciproducens galactitolivorans with reverse β-oxidation-associated redox remodelingopen access
- Authors
- Nair, Pranav Sasidharan; Kim, Hyunjin; Kang, Seongcheol; Jeon, Byoung Seung; Angenent, Largus T.; Sang, Byoung-In
- Issue Date
- Oct-2026
- Publisher
- ELSEVIER SCI LTD
- Keywords
- Microbial chain elongation; Sustainable bioprocessing; Multi-omics; Reducing equivalents
- Citation
- BIORESOURCE TECHNOLOGY, v.458, pp 1 - 11
- Pages
- 11
- Indexed
- SCIE
SCOPUS
- Journal Title
- BIORESOURCE TECHNOLOGY
- Volume
- 458
- Start Page
- 1
- End Page
- 11
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/218686
- DOI
- 10.1016/j.biortech.2026.135089
- ISSN
- 0960-8524
1873-2976
- Abstract
- Medium-chain carboxylic acids, such as n-caproate, are attractive sustainable platform chemicals. However, their microbial production is often limited by electron availability and low product selectivity. This study investigated the effect of hydrogen supplementation on glucose-based n-caproate production by Caproiciproducens galactitolivorans. Batch fermentation was performed under various hydrogen pressures (0 to 600 kPa). At 600 kPa hydrogen, n-caproate reached 8.0 g L−1, accompanied by a 66% increase in n-caproate selectivity and a tenfold increase in the intracellular redox-cofactor ratio, consistent with enhanced redox-cofactor turnover. Multi-omics analysis indicated metabolic remodeling under hydrogen-enriched conditions, including the increased abundance of key enzymes in the reverse β-oxidation pathway and redox-associated functions. In contrast, although fatty acid biosynthesis genes were transcriptionally induced, this transcriptional increase was not reflected at the protein level, suggesting a metabolic response more consistent with reverse β-oxidation-supported n-caproate synthesis than with fatty acid biosynthesis. These results support the use of hydrogen as a clean external reducing agent for improving n-caproate yield and redox efficiency in defined microbial systems. This study provides mechanistic insights into redox-driven metabolic control and selective n-caproate production in a defined microbial chain elongation system.
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