In-Vitro Regeneration of Interspecific F1 Hybrid (Eucalyptus citriodora and Eucalyptus torelliana) of Eucalyptus

Barkha Kamal, I. D. Arya, Sujata Gupta
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引用次数: 1

Abstract

Tissue culture technique was standardized for in vitro shoot multiplication, using nodal segments of 25- 30 years old trees i.e., promising interspecific F1 hybrid of Eucalyptus (Eucalyptus citriodora and Eucalyptus torelliana). Due to the phenolic exudation explants did not survive and eventually died without regenerating buds. The explants collected from July to September were the best for in vitro studies for icropropagation. The axillary buds were surface sterilized with 0.1% Mercuric chloride solution for 10-15 minutes, followed by 0.1% Bavistin treatment for 1 minute and subsequently washed 3-4 times with sterilized distilled water. These surface sterilized axillary buds were cultured on MS medium supplemented with cytokinin and auxin. MS medium supplemented with 1.5mg/l BAP + 0.1mg/l NAA proved to be the best hormonal combination for induction of axillary bud which resulted in the development of 1-3 axillary shoots. The proliferated shoots were cultured on MS medium with different concentration of BAP (0.1 – 3.0 mg/l) alone or in combination with NAA (0.1-1.5mg/l) and supplemented with sucrose at 3%. The aim of the paper was to obtain maximum rate of in vitro regeneration of FRI-15 by using micropropagation technique.
桉树种间F1杂种(桉树和桉树)的离体再生
采用25 ~ 30年树龄的桉树(尤加利citriodora和尤加利torelliana) F1种间杂种的节段为材料,标准化组织培养技术进行离体芽增殖。由于酚渗出,外植体不能存活,最终没有再生芽而死亡。7 ~ 9月采集的外植体最适合体外培养。腋芽表面用0.1%氯化汞溶液消毒10-15分钟,再用0.1%巴伐菌素处理1分钟,然后用消毒蒸馏水清洗3-4次。这些表面灭菌的腋芽在添加细胞分裂素和生长素的MS培养基上培养。MS培养基中添加1.5mg/l BAP + 0.1mg/l NAA是诱导腋芽的最佳激素组合,腋芽发育1-3个。在MS培养基上分别添加不同浓度的BAP (0.1 ~ 3.0 mg/l)和NAA (0.1 ~ 1.5mg/l),并添加3%的蔗糖。本文的目的是利用微繁技术获得最大的fr -15离体再生率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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