Journals / Turkish Journal of Botany / 2011 / Cilt: 35 - Sayı: 1

In vitro propagation of endemic and endangered Muscari mirum from different explant types

Pages
37–43
Publication Date
2011-01-01
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The chromosome number of the root cells of in vitro induced bulblets was diploid 2n = 18.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:A protocol for in vitro propagation of Muscari mirum Speta, an endangered geophyte of the family Hyacinthaceae, was developed.
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Key Findings & Data:Bulb scale, scape, leaf, and immature embryo explants were cultured on different nutrient media compositions supplemented with various concentrations of plant growth regulators (BAP, NAA, TDZ, Picloram, 2,4-D).
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Conclusion & Impact:The chromosome number of the root cells of in vitro induced bulblets was diploid 2n = 18.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Key words: Muscari mirum · in vitro propagation · bulb scale

Abstract

A protocol for in vitro propagation of Muscari mirum Speta, an endangered geophyte of the family Hyacinthaceae, was developed. Bulb scale, scape, leaf, and immature embryo explants were cultured on different nutrient media compositions supplemented with various concentrations of plant growth regulators (BAP, NAA, TDZ, Picloram, 2,4-D). Scape explants produced callus only. Higher numbers of bulblets were obtained from bulb scale explants than embryo explants. The highest percentage of the bulb formation (23.50 per explant) were obtained from bulb scale explants consisting of 4 scale segments cultured on Murashige and Skoog (MS) medium supplemented with 4 mg L-1 6-benzylaminopurine (BAP) and 0.25 mg L-1 a- naphthaleneacetic acid (NAA) after 5 months of culture initiation. Rooted bulblets which were more than 5 mm in diameter were transplanted into potting mixture of soil, vermiculite and perlite (1:1:1). The chromosome number of the root cells of in vitro induced bulblets was diploid 2n = 18.

Özet

A protocol for in vitro propagation of Muscari mirum Speta, an endangered geophyte of the family Hyacinthaceae, was developed. Bulb scale, scape, leaf, and immature embryo explants were cultured on different nutrient media compositions supplemented with various concentrations of plant growth regulators (BAP, NAA, TDZ, Picloram, 2,4-D). Scape explants produced callus only. Higher numbers of bulblets were obtained from bulb scale explants than embryo explants. The highest percentage of the bulb formation (23.50 per explant) were obtained from bulb scale explants consisting of 4 scale segments cultured on Murashige and Skoog (MS) medium supplemented with 4 mg L-1 6-benzylaminopurine (BAP) and 0.25 mg L-1 a- naphthaleneacetic acid (NAA) after 5 months of culture initiation. Rooted bulblets which were more than 5 mm in diameter were transplanted into potting mixture of soil, vermiculite and perlite (1:1:1). The chromosome number of the root cells of in vitro induced bulblets was diploid 2n = 18.

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Cite This Article

NASIRCILAR, A. G., MİRİCİ, S., KARAGÜZEL, Ö., EREN, Ö., BAKTIR, İ. (2011). In vitro propagation of endemic and endangered Muscari mirum from different explant types. Turkish Journal of Botany, Cilt: 35 - Sayı: 1, 37–43. https://ajindex.com/articles/183454

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References (10)

  1. Arslan N, Gürbüz B, Gümüşçü A, Özcan S, Mirici S & Khawar KM (2002). Cultivation of Sternbergia fisheriana (Herbert) Rupr. and a study on its morphological charecteristics. Pak J Bot 34: 411- 418. Atay S (1996). Soğanlı Bitkiler. Türkiye’den İhracatı Yapılan Türlerin Tanıtım ve Üretim Rehberi. İstanbul.
  2. Cha HC, Park HJ & Min BM (2002). Plant regeneration and morphology during in vitro organogenesis from Heloniopsis orientalis (Thunb.) C. Tanaka. J Plant Biol 45: 56-61.
  3. Dirmenci T, Dündar E, Deniz G, Arabacı T, Martin E, Jamzad Z (2010). evaluation of Cyclotrichium: a piece in the tribe Mentheae puzzle. Turk J Bot 34: 59-70. Doğu S & Bağcı Y (2009). Muscari vuralii sp. nov. (Liliaceae/Hyacinthaceae) from South Anatolia, Turkey. Nord J Bot 27: 243-246. Eker İ & Koyuncu M (2008). Muscari babachii sp. nov. (Hyacinthaceae) from South Anatolia. Nord J Bot 26: 49-52.
  4. Ekim T, Koyuncu M, Vural M, Duman H, Aytaç Z & Adıgüzel N (2000). Pteriophyta and Spermatophyta. Red Data Book of Turkish Plants. Barışcan Ofset. Ankara.
  5. Elçi Ş (1994). Sitogenetikte Araştırma Yöntemleri ve Gözlemler. Yüzüncü Yıl Üniversitesi Yayınları, No: 18, pp. 68-69, Van. Huetteman CA & Preece JE (1993). Thidiazuron: a potent cytokinin for woody plant tissue culture. Plant Cell Tiss Org 33: 105-119. Jha S & Sen S (1985). In vitro regeneration of Ruscus hypophyllum L. plants. Plant Cell Tiss Org 5: 79-87.
  6. Kalyoncu DD, İpek A, Parmaksız İ, Arslan N, Sancak C & Özcan S (2006). In vitro bulblet production in wild Tulipa species. Agricultural Constraints in the Soil-Plant Atmosphere Continuum Proceedings of the International Symposium, pp. 289-292.
  7. Ghent, Belgium. McCarton SA & Staden V (1998). Micropropagation of the medicinal plant, Scilla natalensis Planch. Plant Growth Regul 25: 177-180.
  8. Miadokova E, Masterova I, Vlckova V, Duhova V & Toth J (2002). Antimutagenic potential of homoisoflavonoids from Muscari racemosum. J. Ethnopharmacol 81: 381-386.
  9. Mirici S, Parmaksiz İ, Özcan S, Sancak C, Uranbey S, Sarıhan EO, Gümüscü A, Gürbüz B & Arslan A (2005). Efficient in vitro bulblet regeneration from immature embryos of endangered Sternbergia fischeriana. Plant Cell Tiss Org 80: 239-246. Mori S & Nakano M (2004). Somatic embryo induction from leaf-and flower bud-derivied calli in several Muscari species and cultivars. Propag Ornamen Plants 4: 58-62.
  10. Mujlib A, Banerjee S & Ghosh PD (2005). Origin, development and structure of somatic embryos in selected bulbous ornamentals: BAP as inducer. Plant Cell Mon