摘要
应用游离小孢子培养技术,培养茄子体细胞融合杂种DSa不同株系的小孢子。结果表明:对花药进行3C℃高温6 d预处理,能显著提高小孢子脱分化能力;小孢子离体培养的最佳发育时期是单核期;小孢子培养的适宜培养基为KM附加PEG 250 mg/L、2,4-D 0.2 mg/L、ZT 0.5 mg/L、NAA 1mg/L及6.5%的葡萄糖;再生植株适宜培养基为MS附加ZT 2 mg/L、IAA 0.1 mg/L、2%蔗糖和7g/L琼脂。
Somatic fusion hybrid DSa (S. torvum Sw x S. melongena L. ' Dourga' ) microspore were cultured by using isolated microspore culture. The result show that microspore dedifferentiation ability was markedly improved by using the treatment of anther under the high temperature conditions of 36℃ for continuous 6 days. The best development period for microspore culture is monokaryotic stage; The suitable medium for microspore culture is KM with PEG 250 mg/L, 2, 4-D 0. 2 mg/L, ZT 0. 5 mg/L, NAA 1 mg/L and glucose 6.5%; The suitable medium for regenerated plantlet is MS with ZT 2 mg/L, IAA 0. 1 mg/L, sugar 2% and agar 7 g/L.
出处
《园艺学报》
CAS
CSCD
北大核心
2004年第2期233-235,共3页
Acta Horticulturae Sinica
基金
农业部蔬菜遗传与生理重点开放实验室资助项目
国家863计划项目(2002AA244011-1)
欧盟资助项目(ICA4-CT-2001-10064)