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callogenesis of Cork Oak(Quercus suber L.)through In Vitro Culture of Nodes and Internodes

American Journal of Plant Sciences 2017年第8期8卷 1801-1819页

作者： Mohammed L’bachir El Kbiach Brahim El Bouzdoudi Rabah Saidi Zineb Nejjar El Ansari Safaa Rahmouni Ahmed Lamarti Laboratory of Plant Biotechnology Biology Department Faculty of Sciences Abdelmalek Essaadi University Tetouan Morocco Department of Matter and Life Sciences High Normal School Martil Morocco

The present study is about in vitro culture of cork oak, through callogenesis from nodes and internodes, withdrawn from seedlings of three months. These latter were obtained after acorns germination on peat. Nodes showed a high capacity for callogenesis and the best rate was obtained on a medium containing Woody Plant Medium (WPM) macronutrients, Murashige and Skoog (MS) micronutrients and vitamins, 4.5 μM of 6-Benzylaminopurine (BAP), 7 μM of 2-naphthalineacetic acid (NAA) and 30 g/L of Sucrose. Calluses are transplanted onto the same mineral solution, with or without growth regulators, and in the 3rd transplanting;small white embryos appear on the surface of calluses.

关键词： Cork oak Quercus suber L. Nodes Internodes callogenesis

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Micropropagation of Eucalyptus grandis×*** AEC 224 clone

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Journal of Forestry Research 2017年第1期28卷 29-39页

作者： Cassiana de Oliveira Juliana Degenhardt-Goldbach Gisela Manuela de Franca Bettencourt Erika Amano Luziane Franciscon Marguerite Quoirin Department of Plant Science Federal University of Parana1540Rua dos FuneionariosCuritibaParanaBrazil Embrapa-Forest 111Estrada da RibeiraColomboParanaBrazil Department of Technology Federal University of Parana210avenida CelFrancisco Heraiclito dos SantosCuritibaParanaBrazil Department of Botany Federal University of Parana210avenida CelFrancisco Heraiclito dos SantosCuritibaParanaBrazil

Genetic transformation systems require protocols that allow regenerating transgenic plants from transformed tissues. This study aimed to establish a protocol for indirect organogenesis in leaf explants of a Eucalyptus grandis x E. urophylla AEC 224 clone. During callogenesis stage, several concentrations of NAA and then NAA or 2,4-D combined with TDZ were tested in JADS culture medium for 30 days, followed by subculture of the explants in the regeneration medium, containing 5.0 μM BA and 0.5 μM NAA for another 30 days. In these media, the explant oxidation rate was high （95 %）. Thus, in order to reduce oxidation, different ;culture media were compared： WPM, MS, JADS and modified QL, followed by explant transfer onto regeneration medium. The highest percentage of regeneration and the lowest oxidation rate were achieved on WPM medium. Then, NAA and 2,4-D were tested in combination with TDZ and also TDZ and BA combined with NAA in WPM medium. The most efficient culture media in terms of shoot regeneration were WPM supplemented with 0.25 μM TDZ and 0.1μM NAA during 30 days for callus induction and then with 5.0 μM BA and 0.5 μM NAA for another 30 days. This protocol yielded a regeneration rate of 43 %, with a low oxidation of tissues. A rooting experiment was conducted using half strength MS medium and comparing three concentrations of IBA （2.46, 4.90 and 7.35μM）. The highest rooting percentage （35 %） was obtained on medium containing 2.46μM IBA. Once the shoots were rooted, acclimatization in a greenhouse was not challenging and plant survival reached 100 %.

关键词： callogenesis Eucalyptus urograndis Organogenesis WPM culture medium

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Plantlets Regeneration via Somatic Embryogenesis from the Nucellus Tissues of Kinnow Mandarin (Citrus reticulata L.)

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American Journal of Plant Sciences 2016年第6期7卷 798-805页

作者： Mubashir Hussain Naveed Iqbal Raja Muhammad Iqbal Anam Iftikhar Huma Mehreen Sadaf Sidra Sabir Muhammad Asim Sultan Muhammad Nasim Ashraf Faz Department of Botany PMAS Arid Agriculture University Rawalpindi Pakistan Department of Botany University of Sargodha Sargodha Pakistan Department of Botany Government College University Faisalabad Pakistan

Studies were initiated to explore the role of nucellus tissues and growth regulators in plantlets regeneration via somatic embryogenesis of Kinnow mandarin [Citrus reticulata L. (Blanco)]. Nucellus tissues were cultured on MS medium supplemented with different concentrations and combinations of auxins, cytokinins and malt extract for primary callus induction. The best response for primary callus induction (90%) was obtained when MS medium was supplemented with 5 mg/l 2,4-D and 500 mg/l malt extract. Best results for embryogenic callus induction (80%) were obtained in C8 medium. The induction of somatic embryos was highest when MS medium was supplemented with 1 mg/l BAP and maturation of somatic embryos occurred when MS medium was supplemented with 5 mg/l 2,4-D and 1 mg/l BAP. Maximum plantlets were regenerated (92%) from the somatic embryos on half strength MS medium with no hormones. The plantlets were successfully acclimatized in different potting mixtures and highest survival rate (100%) was achieved in potting mixture containing sand and peat moss (2:1).

关键词： Tissue Culture MS Media Citrus Nucellus Tissue callogenesis Somatic Embryos

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