In vitro propagation of Securidaca longipedunculata (Fresen) from shoot tip: an endangered medicinal plant

Abstract Background Securidaca longipedunculata Fresen is an indigenous medicinal plant in Africa that has an important place in both traditional and modern medicine. This plant is endangered because of high seed dormancy, low germination rate, and over exploitation. Therefore, micropropagation meth...

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Main Authors: Teklebrihan Lijalem, Tileye Feyissa
Format: Article
Language:English
Published: SpringerOpen 2020-01-01
Series:Journal of Genetic Engineering and Biotechnology
Subjects:
Online Access:https://doi.org/10.1186/s43141-019-0017-0
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spelling doaj-7d0d6859ffcc4ab4a54aad996e7942832021-01-24T12:42:26ZengSpringerOpenJournal of Genetic Engineering and Biotechnology2090-59202020-01-0118111010.1186/s43141-019-0017-0In vitro propagation of Securidaca longipedunculata (Fresen) from shoot tip: an endangered medicinal plantTeklebrihan Lijalem0Tileye Feyissa1Institute of Biotechnology, Addis Ababa UniversityInstitute of Biotechnology, Addis Ababa UniversityAbstract Background Securidaca longipedunculata Fresen is an indigenous medicinal plant in Africa that has an important place in both traditional and modern medicine. This plant is endangered because of high seed dormancy, low germination rate, and over exploitation. Therefore, micropropagation method is important to address these problems. The objective of this study is to develop a micropropagation protocol for S. longipedunculata from shoot tip explants. Results Among different Clorox concentrations, seeds sterilized with 10% Clorox for 10 min resulted in 85% decontamination and 80% germination. Among different media used to evaluate the rate of seed germination, seeds that were de-coated and transversally cut at the tip and cultured on basal MS medium resulted in 100% germination. The highest percentage of shoot initiation (87%) was obtained on MS medium containing 1.0 mg/l 6-Benzylaminopurine (BAP). The highest mean shoot number per explant (8.5 ± 0.69) was achieved on MS multiplication medium containing 1.5 mg/l BAP in combination with 0.1 mg/l Indole-3-butyric acid (IBA). The highest mean number of roots per explant (3.73 ± 0.69) was obtained on MS medium containing 2.0 mg/l Indole-3-acetic-acid (IAA). Among plantlets transferred to greenhouse, 60% survived after acclimatization. Conclusions This micropropagation protocol can be used for mass propagation of S. longipedunculata that contributes to its conservation and genetic improvement.https://doi.org/10.1186/s43141-019-0017-0MicropropagationPlant growth regulatorsSecuridaca longipedunculataShoot initiationShoot multiplication
collection DOAJ
language English
format Article
sources DOAJ
author Teklebrihan Lijalem
Tileye Feyissa
spellingShingle Teklebrihan Lijalem
Tileye Feyissa
In vitro propagation of Securidaca longipedunculata (Fresen) from shoot tip: an endangered medicinal plant
Journal of Genetic Engineering and Biotechnology
Micropropagation
Plant growth regulators
Securidaca longipedunculata
Shoot initiation
Shoot multiplication
author_facet Teklebrihan Lijalem
Tileye Feyissa
author_sort Teklebrihan Lijalem
title In vitro propagation of Securidaca longipedunculata (Fresen) from shoot tip: an endangered medicinal plant
title_short In vitro propagation of Securidaca longipedunculata (Fresen) from shoot tip: an endangered medicinal plant
title_full In vitro propagation of Securidaca longipedunculata (Fresen) from shoot tip: an endangered medicinal plant
title_fullStr In vitro propagation of Securidaca longipedunculata (Fresen) from shoot tip: an endangered medicinal plant
title_full_unstemmed In vitro propagation of Securidaca longipedunculata (Fresen) from shoot tip: an endangered medicinal plant
title_sort in vitro propagation of securidaca longipedunculata (fresen) from shoot tip: an endangered medicinal plant
publisher SpringerOpen
series Journal of Genetic Engineering and Biotechnology
issn 2090-5920
publishDate 2020-01-01
description Abstract Background Securidaca longipedunculata Fresen is an indigenous medicinal plant in Africa that has an important place in both traditional and modern medicine. This plant is endangered because of high seed dormancy, low germination rate, and over exploitation. Therefore, micropropagation method is important to address these problems. The objective of this study is to develop a micropropagation protocol for S. longipedunculata from shoot tip explants. Results Among different Clorox concentrations, seeds sterilized with 10% Clorox for 10 min resulted in 85% decontamination and 80% germination. Among different media used to evaluate the rate of seed germination, seeds that were de-coated and transversally cut at the tip and cultured on basal MS medium resulted in 100% germination. The highest percentage of shoot initiation (87%) was obtained on MS medium containing 1.0 mg/l 6-Benzylaminopurine (BAP). The highest mean shoot number per explant (8.5 ± 0.69) was achieved on MS multiplication medium containing 1.5 mg/l BAP in combination with 0.1 mg/l Indole-3-butyric acid (IBA). The highest mean number of roots per explant (3.73 ± 0.69) was obtained on MS medium containing 2.0 mg/l Indole-3-acetic-acid (IAA). Among plantlets transferred to greenhouse, 60% survived after acclimatization. Conclusions This micropropagation protocol can be used for mass propagation of S. longipedunculata that contributes to its conservation and genetic improvement.
topic Micropropagation
Plant growth regulators
Securidaca longipedunculata
Shoot initiation
Shoot multiplication
url https://doi.org/10.1186/s43141-019-0017-0
work_keys_str_mv AT teklebrihanlijalem invitropropagationofsecuridacalongipedunculatafresenfromshoottipanendangeredmedicinalplant
AT tileyefeyissa invitropropagationofsecuridacalongipedunculatafresenfromshoottipanendangeredmedicinalplant
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