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An endogenous microRNA (miRNA1166.1) can regulate photobio-H(2) production in eukaryotic green alga Chlamydomonas reinhardtii

BACKGROUND: Hydrogen photoproduction from green microalgae is regarded as a promising alternative solution for energy problems. However, the simultaneous oxygen evolution from microalgae can prevent continuous hydrogen production due to the hypersensitivity of hydrogenases to oxygen. Sulfur deprivat...

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Detalles Bibliográficos
Autores principales: Wang, Yuting, Zhuang, Xiaoshan, Chen, Meirong, Zeng, Zhiyong, Cai, Xiaoqi, Li, Hui, Hu, Zhangli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5930490/
https://www.ncbi.nlm.nih.gov/pubmed/29743954
http://dx.doi.org/10.1186/s13068-018-1126-8
Descripción
Sumario:BACKGROUND: Hydrogen photoproduction from green microalgae is regarded as a promising alternative solution for energy problems. However, the simultaneous oxygen evolution from microalgae can prevent continuous hydrogen production due to the hypersensitivity of hydrogenases to oxygen. Sulfur deprivation can extend the duration of algal hydrogen production, but it is uneconomical to alternately culture algal cells in sulfur-sufficient and sulfur-deprived media. RESULTS: In this study, we developed a novel way to simulate sulfur-deprivation treatment while constantly maintaining microalgal cells in sulfur-sufficient culture medium by overexpressing an endogenous microRNA (miR1166.1). Based on our previous RNA-seq analysis in the model green alga Chlamydomonas reinhardtii, three endogenous miRNAs responsive to sulfur deprivation (cre-miR1166.1, cre-miR1150.3, and cre-miR1158) were selected. Heat-inducible expression vectors containing the selected miRNAs were constructed and transformed into C. reinhardtii. Comparison of H(2) production following heat induction in the three transgenic strains and untransformed control group identified miR1166.1 as the best candidate for H(2) production regulation. Moreover, enhanced photobio-H(2) production was observed with repeated induction of miR1166.1 expression. CONCLUSIONS: This study is the first to identify a physiological function of endogenous miR1166.1 and to show that a natural miRNA can regulate hydrogen photoproduction in the unicellular model organism C. reinhardtii. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1126-8) contains supplementary material, which is available to authorized users.