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April 10, 2026Journal of Eukaryotic Microbiology0 citations

Elucidation of Enzymatic Routes Underlying Odd‐Chain Fatty Acid Synthesis and Propionate Assimilation in Euglena gracilis

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RKRyunosuke KatayamaRHRyuta HayashiMUMitsuhiro Ueda

Key Points

  • The research aims to clarify the enzymatic pathways involved in odd-chain fatty acid synthesis and propionate assimilation in Euglena gracilis.
  • Generated knockout (KO) mutants of candidate enzymes using CRISPR/Cas9.
  • Examined roles of succinyl-CoA synthetase, methylmalonyl-CoA mutase, methylmalonyl-CoA epimerase, and propionyl-CoA carboxylase in lipid biosynthesis.
  • Analyzed the effects of enzyme knockouts on odd-chain wax ester synthesis and propionate assimilation.
  • KO of methylmalonyl-CoA epimerase and propionyl-CoA carboxylase did not affect odd-chain wax ester synthesis.
  • Succinyl-CoA synthetase β1 is necessary for odd-chain wax ester synthesis while β2 is crucial for propionate assimilation.
  • Partial impairment of propionate assimilation was observed in certain knockout strains, suggesting alternative pathways.

Abstract

Wax esters (WEs) produced by Euglena gracilis under anaerobic conditions contain significant proportions of odd-chain fatty acids and fatty alcohols (30%-40%). Propionyl-CoA, the primer for odd-chain fatty acid synthesis, is generally thought to be generated via the methylmalonyl-CoA pathway; however, the enzymatic basis of this pathway in E. gracilis remains unclear. Here, we generated knockout (KO) mutants of candidate enzymes in the methylmalonyl-CoA pathway-succinyl-CoA synthetase (SCS), methylmalonyl-CoA mutase (MCM), methylmalonyl-CoA epimerase (MCE), and propionyl-CoA carboxylase (PCC)-using the CRISPR/Cas9 system and examined their roles in odd-chain fatty acid synthesis and propionate assimilation. The methylmalonyl-CoA pathway exhibited direction-dependent functions. KO of MCE and PCC did not affect the proportion of odd-chain WEs, indicating that these enzymes are not required for odd-chain WE synthesis and suggesting an alternative route converting methylmalonyl-CoA to propionyl-CoA. In contrast, both enzymes were required for propionate assimilation. Functional differentiation was observed between SCSβ isozymes: SCSβ1 contributed to odd-chain WE synthesis, whereas SCSβ2 primarily functioned in propionate assimilation. Partial impairment of propionate assimilation in SCSα or SCSβ2 KO strains suggests involvement of additional routes. These findings improve our understanding of direction-dependent roles in the methylmalonyl-CoA pathway in E. gracilis and support further studies of odd-chain lipid biosynthesis.

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Cite This Study

Katayama et al. (2026) studied this question.

synapsesocial.com/papers/69d893c96c1944d70ce04cf2https://doi.org/10.1111/jeu.70078
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