| Literature DB >> 25860691 |
Masami Nakazawa1, Hiroko Andoh, Keiichiro Koyama, Yomi Watanabe, Takeo Nakai, Mitsuhiro Ueda, Tatsuji Sakamoto, Hiroshi Inui, Yoshihisa Nakano, Kazutaka Miyatake.
Abstract
Euglena gracilis produces wax ester under hypoxic and anaerobic culture conditions with a net synthesis of ATP. In wax ester fermentation, fatty acids are synthesized by reversing beta-oxidation in mitochondria. A major species of wax ester produced by E. gracilis is myristyl myristate (14:0-14:0Alc). Because of its shorter carbon chain length with saturated compounds, biodiesel produced from E. gracilis wax ester may have good cold flow properties with high oxidative stability. We reasoned that a slight metabolic modification would enable E. gracilis to produce a biofuel of ideal composition. In order to produce wax ester with shorter acyl chain length, we focused on isozymes of the enzyme 3-ketoacyl-CoA thiolase (KAT), a condensing enzyme of the mitochondrial fatty acid synthesis pathway in E. gracilis. We performed a gene silencing study of KAT isozymes in E. gracilis. Six KAT isozymes were identified in the E. gracilis EST database, and silencing any three of them (EgKAT1-3) altered the wax ester amount and composition. In particular, silencing EgKAT1 induced a significant compositional shift to shorter carbon chain lengths in wax ester. A model fuel mixture inferred from the composition of wax ester in EgKAT1-silenced cells showed a significant decrease in melting point compared to that of the control cells.Entities:
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Year: 2015 PMID: 25860691 DOI: 10.1007/s11745-015-4010-3
Source DB: PubMed Journal: Lipids ISSN: 0024-4201 Impact factor: 1.880