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Accelerated triacylglycerol production without growth inhibition by overexpression of a glycerol-3-phosphate acyltransferase in the unicellular red alga Cyanidioschyzon merolae.
Fukuda, Satoshi; Hirasawa, Eri; Takemura, Tokiaki; Takahashi, Sota; Chokshi, Kaumeel; Pancha, Imran; Tanaka, Kan; Imamura, Sousuke.
Afiliação
  • Fukuda S; School of Life Science and Technology, Tokyo Institute of Technology, Yokohama, Japan.
  • Hirasawa E; Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, Yokohama, Japan.
  • Takemura T; School of Life Science and Technology, Tokyo Institute of Technology, Yokohama, Japan.
  • Takahashi S; Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, Yokohama, Japan.
  • Chokshi K; Laboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology, Yokohama, Japan.
  • Pancha I; Laboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology, Yokohama, Japan.
  • Tanaka K; Laboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology, Yokohama, Japan.
  • Imamura S; Laboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology, Yokohama, Japan. simamura@res.titech.ac.jp.
Sci Rep ; 8(1): 12410, 2018 08 17.
Article em En | MEDLINE | ID: mdl-30120352
ABSTRACT
Microalgae accumulate triacylglycerols (TAGs), a promising feedstock for biodiesel production, under unfavorable environmental or stress conditions for their growth. Our previous analyses revealed that only transcripts of CmGPAT1 and CmGPAT2, both encoding glycerol-3-phosphate acyltransferase, were increased among fatty acid and TAG synthesis genes under TAG accumulation conditions in the red alga Cyanidioschyzon merolae. In this study, to investigate the role of these proteins in TAG accumulation in C. merolae, we constructed FLAG-fused CmGPAT1 and CmGPAT2 overexpression strains. We found that CmGPAT1 overexpression resulted in marked accumulation of TAG even under normal growth conditions, with the maximum TAG productivity increased 56.1-fold compared with the control strain, without a negative impact on algal growth. The relative fatty acid composition of 182 in the TAGs and the sn-1/sn-3 positions were significantly increased compared with the control strain, suggesting that CmGPAT1 had a substrate preference for 182. Immunoblot analysis after cell fractionation and immunostaining analysis demonstrated that CmGPAT1 localizes in the endoplasmic reticulum (ER). These results indicate that the reaction catalyzed by the ER-localized CmGPAT1 is a rate-limiting step for TAG synthesis in C. merolae, and would be a potential target for improvement of TAG productivity in microalgae.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Triglicerídeos / Expressão Gênica / Rodófitas / Glicerol-3-Fosfato O-Aciltransferase Idioma: En Revista: Sci Rep Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Triglicerídeos / Expressão Gênica / Rodófitas / Glicerol-3-Fosfato O-Aciltransferase Idioma: En Revista: Sci Rep Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Japão