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Comparison of Lisianthus (Eustoma grandiflorum) Cultivars Based on the Selected Regeneration Media Using Anther Culture

机译:利用花药培养物选择再生培养基比较桔梗品种的比较

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Double haploids in lisianthus cultivars were produced using anther culture. The anther of 'Art Peach' was cultured on the Murashige and Skoog (MS) medium with 3% sucrose with auxin and cytokinin. The highest frequency of calli developed from anthers (100%) and green plantlets per100 calli (60 regenerants) was observed on the medium containing 8 mgL~(-1)N6 benzyladenine (BA) and 0.1mg-L~(-1) naphthaleneacetic acids (NAA). When anthers were cultured on the medium supplemented with 2 mg L~(-1) BA and 0.5 mg-L~(-1) NAA, 33.3% of calli formed plantlets. Using the anther culture, callus induction and plantlets regeneration in five cultivars were developed differently, suggesting that the genotype might predetermined anther culture response. These resultsindicate that a highly efficient new microprogation technique can be provided by anther culture in vitro for lisianthus. Anther culture in vitro can provide a highly efficient new microprogation technique for lisianthus.
机译:使用花药培养在桔梗品种中产生双单倍体。 'Art Peach'的花药在Murashige和Skoog(MS)培养基中培养,培养基中含3%的蔗糖,生长素和细胞分裂素。在含有8 mgL〜(-1)N6苄腺嘌呤(BA)和0.1mg-L〜(-1)萘乙酸的培养基上,花药(100%)和每100个愈伤组织的绿色小植株发育的愈伤组织出现频率最高(60个再生体)。酸(NAA)。当在补充有2 mg L〜(-1)BA和0.5 mg-L〜(-1)NAA的培养基上培养花药时,愈伤组织形成了33.3%的幼苗。使用花药培养,五个品种的愈伤组织诱导和幼苗再生的发育不同,表明该基因型可能预定了花药培养响应。这些结果表明,通过桔梗的花药体外培养可以提供高效的新的微繁殖技术。体外花药培养可为桔梗提供高效的新微繁殖技术。

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