No. 22 (2006)
Articles

Micropropagation of Rudbeckia hirta L. from seedling explants

Published May 23, 2006
Pál Szarvas
Debreceni Egyetem Agrártudományi Centrum, Zöldségtermesztési Tanszék, Orsós Ottó laboratórium, Debrecen
Anikó Zsila-André
Debreceni Egyetem Agrártudományi Centrum, Zöldségtermesztési Tanszék, Orsós Ottó laboratórium, Debrecen
Zoltán Kovács
Gyümölcs- és Dísznövénytermesztési Kutató-Fejlesztő Kht, Budatétény
Miklós Gábor Fári
Debreceni Egyetem Agrártudományi Centrum, Zöldségtermesztési Tanszék, Orsós Ottó laboratórium, Debrecen
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APA

Szarvas, P., Zsila-André, A., Kovács, Z., & Fári, M. G. (2006). Micropropagation of Rudbeckia hirta L. from seedling explants. Acta Agraria Debreceniensis, (22), 53-59. https://doi.org/10.34101/actaagrar/22/3191

We conducted experiments for developing an in vitro micropropagation protocol starting from meristems of Rudbeckia hirta L seedlings. We pre-soaked the seeds in sterile ion-exchanged water for 17 hours, and then achieved surface disinfection in two separate steps. First, we used concentrated household sodium-hypochloride solution for 20 minutes and, also for 20 minutes, we applied hydrogen peroxide of 10%, which was followed by washing with sterile ion-exchanged water three times. For the propagation of seedling meristems, the combination of half-strength solid Murashige and Skoog (1962) culture medium containing 10 mg/l of kinetin and 2 mg/l of kinetin + 0.1 mg/l of 2iP proved to be the most suitable. The average number of shoot-buds developed from the seedling axillary meristem in the best culture media varied between 5 and 17. Without separating them, we inoculated the shoot-bud clusters on MS culture medium containing 2 mg/l of IAA. After four weeks of incubation, we obtained elongated shoots, which we separated and inoculated into a new culture medium and from which we obtained elongated roots. The rooted plants were gradually acclimatised in the cultivation room, potted and carried to a greenhouse, and then planted in open field for subsequent observation. By adopting this method, our laboratory started the micropropagation of the superior and/or elite genotypes of the Rudbeckia hirta L. being of special value in respectt to breeding.

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