Estudios en la germinación y propagación in vitro de tres especies de Leguminosae: Calopogonium sp.,Stylosantes capitata Y Cassia moschata.

Melvin Maiquetía, Edith Teresa Vargas, Marcia Josefina Toro García, E. D. García
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Abstract

Calopogonium sp., Stylosanthes capitata and Cassia moschata, are important legumes in savanna ecosystems that present limitations in their crop production, due to the dormancy of their seeds. In this investigation, we analyzed the seeds germination, in a humid chamber, and in vitro conditions in Murashige and Skoog (1962) medium. The seeds were previously subjected to scarification with ethanol (Calopogonium sp.), and immersion in sulfuric acid (C. moschata and S. capitata). In the humid chamber, the germination values were 60%, Calopogonium sp., 40%, C. moschata and 8% S. capitata. Germination in vitro, at 21 days of culture for Calopogonium sp., was 100%, for S. capitata 85% and for C. moschata 65%. To establish a massive propagation, isolated micro-cuttings of seedlings obtained by germination were cultivated in vitro. Three multiplication media consisting of MS media (1962) supplemented with benzyladenine (0.5; 1; 1.5 mg L), named MS1, MS2 and MS3, respectively, were tested. Calopogonium sp., growing in MS2 and MS3 media showed formation and multiplication of shoots. The highest value was obtained in MS3 (5 shoots / explant). C. moschata formed shoots in MS3 (1.66 shoots/explant). S. capitata formed shoots in all three media, reaching 7.5 shoots/explants in MS3 medium.
豆科植物Calopogonium sp.、Stylosantes capitata和Cassia moschata的萌发和离体繁殖研究。
Calopogonium sp., Stylosanthes capitata和Cassia moschata是稀树草原生态系统中重要的豆科植物,由于其种子的休眠,其作物产量受到限制。在这项调查中,我们分析了种子在潮湿室中的萌发情况,以及在Murashige和Skoog(1962)培养基中的离体条件。先用乙醇(Calopogonium sp.)对种子进行刻蚀,然后用硫酸(C. moschata和S. capitata)浸泡。在潮湿室内,萌发率分别为60%、卡罗波果、40%、莫沙塔和8%。在体外培养21 d时,Calopogonium sp.的萌发率为100%,S. capitata为85%,C. moschata为65%。为了建立大规模繁殖,对萌发获得的幼苗进行了离体培养。三种增殖培养基,由MS培养基(1962)添加苄腺嘌呤(0.5;1;分别命名为MS1、MS2和MS3,分别为1.5 mg L。在MS2和MS3培养基上生长的卡洛波根属植物均有芽的形成和增殖。以MS3最高(5芽/外植体)。柽柳在MS3中形成芽(1.66个芽/外植体)。三种培养基均能形成新芽,在MS3培养基上可达7.5枝/外植体。
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