Conservation Potential Trough In Vitro Regeneration of Two Threatened Medicinal Plants Ungernia sewertzowii and U. victoris

Author:

Mustafina Feruza Usmanovna1ORCID,Juraeva Hanifabonu Kobul kizi1,Jamalova Dilafruz Nematilla kizi2,Hazratov Abbos Tulkin ogli1,Janabaeva Ayimxan Jalgasbaevna1,Kim Hoe Jin3,Na Chae Sun3ORCID,Lee Min Sung3,Oh Yu Jin3ORCID,Tojibaev Komiljon Sharobiddinovich2,Abdinazarov Sodikjon Kholiknazarovich1

Affiliation:

1. Tashkent Botanical Garden Named after Acad. F.N. Rusanov of the Institute of Botany of the Academy of Sciences of the Republic of Uzbekistan, Tashkent 100140, Uzbekistan

2. Institute of Botany of the Academy of Sciences of the Republic of Uzbekistan, Tashkent 100125, Uzbekistan

3. Baekdudaegan National Arboretum, Bonghwa 36209, Republic of Korea

Abstract

Ungernia sewertzowii (US) and U. victoris (UV) are medicinal plants and sources of biologically active compounds for pharmaceutical needs. The leaves of US contain 0.29–0.81% sum of alkaloids with a predominance of lycorine, which is 0.04–0.46% in leaves and 0.15–0.38% in bulbs. Lycorine is used to treat acute and chronic bronchitis. The leaves of UV contain 0.27–0.71% sum of alkaloids with a predominance of galanthamine—0.13–1.15%. Galanthamine is used to treat mild-to-moderate dementia (Alzheimer’s disease). The natural populations of US and UV are in danger as sources of income for local people. To resolve this problem, two protocols for microclonal propagation were developed to replace natural raw materials with in vitro regenerated plants. Callusogenesis of US and UV was induced on Murashige and Skoog (MS) nutrient media with 2.4D (0.5 mg/L) in combination with BAP (0.5 mg/L), Kin (0.5 mg/L), or Zea (0.5 mg/L). Direct (for US) and indirect (for US and UN) organogenesis were observed on MS with BAP (0.5 mg/L) or Kin (0.5 mg/L) in combination with IAA (0.5 mg/L) or NAA (0.5 mg/L). Direct organogenesis resulted in 3–5 bulbs of US on one explant; indirect organogenesis resulted in up to 100–150 bulbs of US and UV on one explant within 6 months, or five to six subcultures after transferring the callus to the nutrient medium. The tissue cultures of US and UV were characterized by very low data on antioxidant activity based on IC50 values for DPPH and ABTS radical scavenging activities, whereas in vitro regenerated plants (leaves and bulbs) had higher data. We concluded that in vitro regenerated plants are valuable sources of lycorine and galanthamine, which allow the protection of the natural populations of these two species from extinction.

Funder

Baekdudaegan National Arboretum

Institute of Botany of the Academy of Sciences of the Republic of Uzbekistan

Tashkent Botanical Garden

Publisher

MDPI AG

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