Efficient plant regeneration from embryogenic cell suspension cultures of Euonymus alatus

Abstract To establish an efficient plant regeneration system from cell suspension cultures of Euonymus alatus, embryogenic callus formation from immature embryos was investigated. The highest frequency of embryogenic callus formation reached 50% when the immature zygotic embryos were incubated on Mu...

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Main Authors: Hyun-A Woo, Seong Sub Ku, Eun Yee Jie, HyeRan Kim, Hyun-Soon Kim, Hye Sun Cho, Won-Joong Jeong, Sang Un Park, Sung Ran Min, Suk Weon Kim
Format: Article
Language:English
Published: Nature Portfolio 2021-07-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-94597-4
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author Hyun-A Woo
Seong Sub Ku
Eun Yee Jie
HyeRan Kim
Hyun-Soon Kim
Hye Sun Cho
Won-Joong Jeong
Sang Un Park
Sung Ran Min
Suk Weon Kim
author_facet Hyun-A Woo
Seong Sub Ku
Eun Yee Jie
HyeRan Kim
Hyun-Soon Kim
Hye Sun Cho
Won-Joong Jeong
Sang Un Park
Sung Ran Min
Suk Weon Kim
author_sort Hyun-A Woo
collection DOAJ
description Abstract To establish an efficient plant regeneration system from cell suspension cultures of Euonymus alatus, embryogenic callus formation from immature embryos was investigated. The highest frequency of embryogenic callus formation reached 50% when the immature zygotic embryos were incubated on Murashige and Skoog (MS) medium supplemented with 1 mg/L 2,4-dichlorophenoxy acetic acid (2,4-D). At higher concentrations of 2,4-D (over 2 mg/L), the frequency of embryogenic callus formation declined significantly. The total number of somatic embryos development was highest with the 3% (w/v) sucrose treatment, which was found to be the optimal concentration for somatic embryo formation. Activated charcoal (AC) and 6-benzyladenine (BA) significantly increased the frequency of plantlet conversion from somatic embryos, but gibberellic acid (GA3) had a negative effect on plantlet conversion and subsequent development from somatic embryos. Even though the cell suspension cultures were maintained for more than 1 year, cell aggregates from embryogenic cell suspension cultures were successfully converted into normal somatic embryos with two cotyledons. To our knowledge, this is the first successful report of a plant regeneration system of E. alatus via somatic embryogenesis. Thus, the embryogenic cell line and plant regeneration system established in this study can be applied to mass proliferation and production of pharmaceutical metabolite in E. alatus.
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spelling doaj.art-0431f00fb2e44e1196202f15786274b22022-12-21T22:55:47ZengNature PortfolioScientific Reports2045-23222021-07-011111910.1038/s41598-021-94597-4Efficient plant regeneration from embryogenic cell suspension cultures of Euonymus alatusHyun-A Woo0Seong Sub Ku1Eun Yee Jie2HyeRan Kim3Hyun-Soon Kim4Hye Sun Cho5Won-Joong Jeong6Sang Un Park7Sung Ran Min8Suk Weon Kim9Plant Systems Engineering Research Center, Korea Research Institute of Bioscience and BiotechnologyPlant Systems Engineering Research Center, Korea Research Institute of Bioscience and BiotechnologyBiological Resource Center, Korea Research Institute of Bioscience and BiotechnologyPlant Systems Engineering Research Center, Korea Research Institute of Bioscience and BiotechnologyPlant Systems Engineering Research Center, Korea Research Institute of Bioscience and BiotechnologyPlant Systems Engineering Research Center, Korea Research Institute of Bioscience and BiotechnologyPlant Systems Engineering Research Center, Korea Research Institute of Bioscience and BiotechnologyDepartment of Crop Science, Chungnam National UniversityPlant Systems Engineering Research Center, Korea Research Institute of Bioscience and BiotechnologyBiological Resource Center, Korea Research Institute of Bioscience and BiotechnologyAbstract To establish an efficient plant regeneration system from cell suspension cultures of Euonymus alatus, embryogenic callus formation from immature embryos was investigated. The highest frequency of embryogenic callus formation reached 50% when the immature zygotic embryos were incubated on Murashige and Skoog (MS) medium supplemented with 1 mg/L 2,4-dichlorophenoxy acetic acid (2,4-D). At higher concentrations of 2,4-D (over 2 mg/L), the frequency of embryogenic callus formation declined significantly. The total number of somatic embryos development was highest with the 3% (w/v) sucrose treatment, which was found to be the optimal concentration for somatic embryo formation. Activated charcoal (AC) and 6-benzyladenine (BA) significantly increased the frequency of plantlet conversion from somatic embryos, but gibberellic acid (GA3) had a negative effect on plantlet conversion and subsequent development from somatic embryos. Even though the cell suspension cultures were maintained for more than 1 year, cell aggregates from embryogenic cell suspension cultures were successfully converted into normal somatic embryos with two cotyledons. To our knowledge, this is the first successful report of a plant regeneration system of E. alatus via somatic embryogenesis. Thus, the embryogenic cell line and plant regeneration system established in this study can be applied to mass proliferation and production of pharmaceutical metabolite in E. alatus.https://doi.org/10.1038/s41598-021-94597-4
spellingShingle Hyun-A Woo
Seong Sub Ku
Eun Yee Jie
HyeRan Kim
Hyun-Soon Kim
Hye Sun Cho
Won-Joong Jeong
Sang Un Park
Sung Ran Min
Suk Weon Kim
Efficient plant regeneration from embryogenic cell suspension cultures of Euonymus alatus
Scientific Reports
title Efficient plant regeneration from embryogenic cell suspension cultures of Euonymus alatus
title_full Efficient plant regeneration from embryogenic cell suspension cultures of Euonymus alatus
title_fullStr Efficient plant regeneration from embryogenic cell suspension cultures of Euonymus alatus
title_full_unstemmed Efficient plant regeneration from embryogenic cell suspension cultures of Euonymus alatus
title_short Efficient plant regeneration from embryogenic cell suspension cultures of Euonymus alatus
title_sort efficient plant regeneration from embryogenic cell suspension cultures of euonymus alatus
url https://doi.org/10.1038/s41598-021-94597-4
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