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首页> 外文期刊>Indian Journal of Biotechnology >Germination of immature embryos and multiplication of Malaxis acuminata D. Don, an endangered therapeutically important orchid, by asymbiotic culture in vitro
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Germination of immature embryos and multiplication of Malaxis acuminata D. Don, an endangered therapeutically important orchid, by asymbiotic culture in vitro

机译:未成熟胚胎的萌发和Malaxis Acuminata D. Day的繁殖,濒危治疗重要兰花,在体外呈偶联培养

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摘要

The effect of culture conditions and developmental stages of embryos on asymbiotic germination of immature seeds of Malaxis acuminata D. Don, an endangered therapeutically important terrestrial orchid, was investigated. Immature seeds of similar to 7-8 wk after pollination (WAP) were germinated on MS medium containing sucrose (3%, w/v) and alpha-naphthalene acetic acid (NAA; 4 mu M) under diffused light condition (20 mu mol m(-2) s(-1)), where about 85% seeds germinated after 135 d of culture. The full light condition (40 mu mol m(-2) s(-1)) did not support healthy germination. The germinated seeds converted into protocorm-like bodies (PLBs) and further differentiated into young plantlets on the same germination medium. The rooted plantlets with well expanded leaves and distinct pseudobulb were achieved on MS medium containing sucrose (3%), activated charcoal (AC; 0.3%, w/v), and NAA and benzyl adenine (BA) (3 mu M each in combination), where as many as 18 shoot buds/PLBs developed per subculture. Amongst the three different organic carbon sources and two basal media tested, only sucrose supported the optimum plant growth and culture proliferation when maintained on MS medium. Incorporation of AC (0.3%) in the regeneration medim accelerated the culture proliferation and distinct pseudobulb formation. The hardened plants transferred to potting mix and maintained in the polyhouse (75% shade) before transferring to the wild, where similar to 75% transplants survived after 2 months of transfer.
机译:研究了培养条件和胚胎发育阶段对Malaxis Acuminata D. Duation植物未成熟种子的脱盐萌发的影响。研究了濒危治疗重要的陆地兰花。在含有蔗糖(3%,w / v)和α-萘乙酸(Naa; 4 mu m)的MS培养基中萌发在含有蔗糖(3%,w / v)和α-萘乙酸(Naa; 4 mu m)下的未成熟种子在扩散的光条件下(20μmol m(-2)s(-1)),约85%的种子在135 d培养后发芽。全灯条件(40μmmolm(-2)s(-1))不支持健康发芽。发芽的种子转化为像素状物体(PLBS),并进一步分化为同一萌发介质的幼儿。含有良好膨胀叶片和明显的假蛋白的根茎植株在含有蔗糖(3%),活性炭(AC; 0.3%,W / V)和NAA和苄基腺嘌呤(BA)上(各组合3μm ),在每个亚栽培中开发的多达18个芽芽/ PLBS。在三种不同的有机碳源和两个基础培养基中,在维持在MS培养基时,仅蔗糖支持最佳植物生长和培养增殖。再生在再生Medim中的AC(0.3%)加速了培养增殖和不同的假脉冲形成。将硬化植物转移到灌封混合物中并在转移到野外,在聚室(75%的阴影)中,在2个月的转移后,类似于75%的移植物。

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