RNAi-based targeted gene knockdown in the model oleaginous microalgae Nannochloropsis oceanica

Overview
TitleRNAi-based targeted gene knockdown in the model oleaginous microalgae Nannochloropsis oceanica
AuthorsWei L, Xin Y, Wang Q, Yang J, Hu H, Xu J
TypeJournal Article
Journal NameThe Plant journal : for cell and molecular biology
Volume89
Issue6
Year2017
Page(s)1236-1250
CitationWei L, Xin Y, Wang Q, Yang J, Hu H, Xu J. RNAi-based targeted gene knockdown in the model oleaginous microalgae Nannochloropsis oceanica. The Plant journal : for cell and molecular biology. 2017 Mar; 89(6):1236-1250.

Abstract

Microalgae are promising feedstock for renewable fuels such as biodiesel, yet development of industrial oleaginous strains has been hindered by the paucity and inefficiency of reverse genetics tools. Here we established an efficient RNAi-based targeted gene-knockdown method for Nannochloropsis spp., which are emerging model organisms for industrial microalgal oil production. The method achieved a 40-80% success rate in Nannochloropsis oceanica strain IMET1. When transcript level of one carbonic anhydrase (CA) was inhibited by 62-83% via RNAi, mutant cells exhibited photosynthetic oxygen evolution (POE) rates that were 68-100% higher than wild-type (WT) at pH 6.0, equivalent to WT at pH 8.2, yet 39-45% lower than WT at pH 9.0. Moreover, the mutant POE rates were negatively correlated with the increase of culture pH, an exact opposite of WT. Thus, a dynamic carbon concentration mechanism (CCM) that is highly sensitive to pH homeostasis was revealed, where the CA inhibition likely partially abrogated the mechanism that normally deactivates CCM under a high level of dissolved CO

Properties
Additional details for this publication include:
Property NameValue
Journal CountryEngland
Publication TypeJournal Article
Language Abbreng
LanguageEnglish
Copyright© 2016 The Authors The Plant Journal © 2016 John Wiley & Sons Ltd.
Elocation10.1111/tpj.13411
DOI10.1111/tpj.13411
Journal AbbreviationPlant J.
Publication Date2017 Mar
eISSN1365-313X
ISSN1365-313X
Publication ModelPrint-Electronic
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PMID: PubMedPMID:28188644