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首页> 外文期刊>African Journal of Biotechnology >Micropropagation and in vitro germplasm conservation of endangered Musa balbisiana Kluai Hin (BBB group)
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Micropropagation and in vitro germplasm conservation of endangered Musa balbisiana Kluai Hin (BBB group)

机译:濒临灭绝的Musa balbisiana Kluai Hin(BBB组)的微繁殖和体外种质保护

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Multiple shoot formation of edible bananas (Musa?balbisiana, BBB group)?‘Kluai Hin’was achieved through organogenesis in bud culture. Excised apical and lateral buds were cultured on a modified?Murashige and Skoog (MS) medium supplemented with22 μM BA and 15% (v/v) coconut water (CW). For mass multiplication, the proliferated shoots were subcultured to MS media containing several concentrations of BA and TDZ. The highest shoot numbers was 21.2 shoots per explant when subcultured to MS medium supplemented with 44 μM BA. Shoot produced roots within 7 days on MS basal medium without plant growth regulator. Microshoots of?‘Kluai Hin’ were stored?in 4 different conditions and on three types of carbon sources (including, sucrose, glucose and sorbitol) at the concentrations of 1, 3 or 5%. Results revealed that sucrose was the suitable carbon source for storing microshoots of ‘Kluai Hin’ at 25°C under a 16 h photoperiod for 6 months. Alginate encapsulation of microshoots for conservation of?‘Kluai Hin’ was established as well.?Microshoots excised from multiple shoot cultures were encapsulated in 3% sodium alginate prepared in MS medium and complexed with 50 mM calcium chloride. Maximum conversion frequency of 73% was noted from encapsulated microshoots cultured on MS medium supplemented with 22 μM BA. Plantlets developed from encapsulation were successfully transferred to field conditions and all the resultant plants were shown to be morphologically normal.
机译:食用香蕉(Musa?balbisiana,BBB组)?'Kluai Hin'的多芽形成是通过芽培养中的器官发生来实现的。顶端和侧芽在改良的Murashige和Skoog(MS)培养基上培养,培养基上添加了22μMBA和15%(v / v)椰子水(CW)。为了大量繁殖,将增殖的芽继代培养至含有数个浓度的BA和TDZ的MS培养基中。当传代至补充有44μMBA的MS培养基中时,最高的芽数是每个外植体21.2芽。在没有植物生长调节剂的MS基础培养基上,芽在7天内产生了根。 “ Kluai Hin”的微缩照片在4种不同条件下以1、3或5%的浓度存储在三种碳源(包括蔗糖,葡萄糖和山梨糖醇)上。结果表明,蔗糖是用于在25°C,16 h光照周期下将'Kluai Hin'的显微照片存储6个月的合适碳源。还建立了用于保存“ Kluai Hin”的微芽的藻酸盐包囊。将从多种芽培养​​物中切下的微芽包囊在MS培养基中制备的3%海藻酸钠中,并与50 mM氯化钙复合。从在添加了22μMBA的MS培养基上培养的包囊微芽中可以看到73%的最大转化频率。从封装中培育出的小植株已成功转移到田间条件下,所有所得植株在形态上均显示正常。

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