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Plant Molecular Biology

, Volume 98, Issue 4–5, pp 319–331 | Cite as

Frond transformation system mediated by Agrobacterium tumefaciens for Lemna minor

  • Gui-Li Yang
  • Yang Fang
  • Ya-Liang Xu
  • Li Tan
  • Qi Li
  • Yang Liu
  • Fan Lai
  • Yan-Ling Jin
  • An-Ping Du
  • Kai-Ze He
  • Xin-Rong Ma
  • Hai Zhao
Article
  • 225 Downloads

Abstract

The Lemnaceae, known as duckweed, the smallest flowering aquatic plant, shows promise as a plant bioreactor. For applying this potential plant bioreactor, establishing a stable and efficient genetic transformation system is necessary. The currently favored callus-based method for duckweed transformation is time consuming and genotype limited, as it requires callus culture and regeneration, which is inapplicable to many elite duckweed strains suitable for bioreactor exploitation. In this study, we attempted to establish a simple frond transformation system mediated by Agrobacterium tumefaciens for Lemna minor, one of the most widespread duckweed species in the world. To evaluate the feasibility of the new transformation system, the gene CYP710A11 was overexpressed to improve the yield of stigmasterol, which has multiple medicinal purposes. Three L. minor strains, ZH0055, D0158 and M0165, were transformed by both a conventional callus transformation system (CTS) and the simple frond transformation system (FTS). GUS staining, PCR, quantitative PCR and stigmasterol content detection showed that FTS can produce stable transgenic lines as well as CTS. Moreover, compared to CTS, FTS can avoid the genotype constraints of callus induction, thus saving at least half of the required processing time (CTS took 8–9 months while FTS took approximately 3 months in this study). Therefore, this transformation system is feasible in producing stable transgenic lines for a wide range of L. minor genotypes.

Keywords

Duckweed Lemna minor Frond transformation system Agrobacterium tumefaciens Plant bioreactor Stigmasterol 

Notes

Acknowledgements

This study was supported by the National Key Technology R&D Program of China (2015BAD15B01), the National Natural Science for General Foundation of China (31770395), Key deployment projects of Chinese Academy of Sciences (ZDRW-ZS-2017-2-1), Science and Technology Service Network Initiative of Chinese Academy of Sciences (KFJ-STS-ZDTP-008); Science & Technology Program of Sichuan Province (2017NZ0018 and 2017HH0077), and the Key and Open Fund of Key Laboratory of Environmental and Applied Microbiology, Chinese Academy of Sciences (KLEAMCAS201501, KLCAS-2014-05 and KLCAS-2016-02).

Author contributions

HZ, XRM, GLY and YF conceived the research. GLY and XRM performed experiments. GLY and XRM analyzed the data and wrote the manuscript. YLX, LT, QL, YL, FL, YLJ, APD, and KZH contributed partial experiments.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest.

Supplementary material

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Supplementary material 1 (TIF 6160 KB)
11103_2018_778_MOESM2_ESM.tif (26.9 mb)
Supplementary material 2 (TIF 27513 KB)
11103_2018_778_MOESM3_ESM.docx (14 kb)
Supplementary material 3 (DOCX 13 KB)

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Copyright information

© Springer Nature B.V. 2018

Authors and Affiliations

  1. 1.Key Laboratory of Environmental and Applied Microbiology, Chengdu Institute of BiologyChinese Academy of SciencesChengduChina
  2. 2.Environmental Microbiology Key Laboratory of Sichuan ProvinceChengduChina
  3. 3.University of Chinese Academy of SciencesBeijingChina

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