In vitro shoot propagation and regeneration of rocket (Eruca sativa Mill.) using organogenesis and somatic embryogenesis
2022
Аутори:
Vinterhalter, Branka![](/themes/MirageIBISS/images/orcid.png)
Krstić-Milošević, Dijana
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Petrović, Mirjana
Devrnja, Nina
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Banjac, Nevena
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Остала ауторства
Špela, BaeblerMarina, Dermastia
Tine, Grebenec
Eva, Praprotnik
Jaka, Razinger
Andreja, Urbanek Krajnc
Тип документа:
Конференцијски прилог (Објављена верзија)
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© 2022 by the Slovenian Society of Plant Biology
Метаподаци
Приказ свих података о документуАпстракт:
Eruca sativa (rocket, Brassicaceae), is known in traditional medicine for its therapeutic, while young plants are used as salad, vegetable, or green foods. Genetic improvement of the rocket has been limited due to the appearance of biennial plants and the requirement for isolation barriers. Plant tissue culture offers a platform to overcome existing barriers to improving this species. The present study aimed to achieve a feasible protocol for shoot regeneration and propagation of rocket cv. Domaća rukola and to evaluate the use of AgNO3 to improve regeneration efficiency. Proliferation of shoots from seedling epicotyl, shoot organogenesis from root, hypocotyl and cotyledon seedling explants, and somatic embryogenesis from immature zygotic embryos were studied. Murashige and Skoog (MS) basal medium in combination with a low KIN concentration of 0.1 mg l-1 with frequent subculture over a period of 3 weeks was found to be optimal for shoot multiplication with a multiplication index of almost 3 and only 9.3% of vitrified shoots without necrosis. Different concentrations of 2,4-D, BA or TDZ in combination with NAA and with or without AgNO3 were tested for shoot regeneration from seedling explants. As a result, the hypocotyl explants cultured on MS with a combination of TDZ 1.0+NAA 0.1+AgNO3 5.0 mg l-1 provided healthy shoots with a satisfactory regeneration rate of 25.4% and 2.2 mean number of shoots per regenerating explant. Immature zygotic embryos cultured on MS medium containing 1.0 mg l-1 2.4-D showed the highest regeneration frequency (78.76%) as well as the number of regenerated somatic embryos per explant (5.13) with low incidence of callusing and necrosis. KIN at 0.5 mg l-1 enabled the best conversion of somatic embryos into healthy plants (22.5%). The results provide an opportunity to use established regeneration protocols in rocket breeding improvement programs.
Кључне речи:
plant tissue culture; TDZ; NAA; Eruca sativaФинансирање / пројекти:
- Министарство науке, технолошког развоја и иновација Републике Србије, институционално финансирање - 200007 (Универзитет у Београду, Институт за биолошка истраживања 'Синиша Станковић') (RS-MESTD-inst-2020-200007)
У:
- Baebler Š, Dermastia M, Grebenc T, Praprotnik E, Razinger J, Urbanek Krajnc A, editors. Book of abstracts: Plants in Changing Environment: International conference of the Slovenian Society of Plant Biology; 2022 Sep 15-16; Ljubljana, Slovenia. Ljubljana: Slovenian Society of Plant Biology; 2022. p. 18.