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作 者:陈绪清[1] 李宏潮[1] 杜运鹏[1] 张铭芳 薛静[1] 杨凤萍[1] 张秀海[1] CHEN Xu-qing;LI Hong-chao;DU Yun-peng;ZHANG Ming-fang;XUE Jing;YANG Feng-ping;ZHANG Xiu-hai(Cichorium endivia L.;mesophyll protoplast;callus; embryogenesis; plant regeneration)
出 处:《黑龙江农业科学》2017年第10期21-25,共5页Heilongjiang Agricultural Sciences
基 金:北京市农林科学院科研创新能力建设专项资助项目(KJCX20150204)
摘 要:为了进行体细胞杂交和基因工程改造的尝试,采用10mL酶解液处理12h,1g鲜重叶片游离出4.5~5.9×106个原生质体,生活率达78%~85%。原生质体分别用3种培养基进行培养,以软化菊苣种子无菌苗的叶片为起始材料进行了叶肉原生质体分离、培养和植株分化的研究,并建立高频率的植株再生系统。结果表明:最适合培养基为改良KMP,原生质体的分裂率和植板率分别达到48.0%和27.5%。同时对原生质体培养的时间长度与愈伤组织的胚胎发生能力及植株分化频率进行了试验比较,培养时间28~41d为最佳时间,愈伤组织的胚性(81.2%)和分化率(70.9%)最高;培养时间42~55d,胚性愈伤及植株分化的比例分别为55.0%和45.2%;培养时间56~69d,愈伤组织的胚性(22.5%)和分化率(16.5%)较差。原生质体再生植株在不含激素的1/2MS培养基上,部分植株直接生根,未生根植株转至1/2MS+IBA 0.3mg·L^(-1)+0.1%活性碳可以生根。In order to make attempts on somatic hybridization and gene transformation,a procedure for high frequency plant regeneration from chicory(Cichorium endivia L.)mesophyll protoplasts was developed by using leaves of an in vitro seedling culture as starting materials.Protoplasts with yields of4.5~5.9×106,were routinely released from one gram fresh leaf which was digested in10mL of an enzyme solution for12h.After careful rinsing and purification,viability of protoplasts ranged from78%to85%.With the aim at selecting a suitable culture medium,three different media were employed to compare their efficiency in protoplast culture.The results showed that the medium“modified KMP”proved the best,leading to highest rates in cell division(48.0%)and plating efficiency(27.5%),respectively.It was found the length of culture period affected either embryogenesis or regeneration of protoplasts,optimal period was28~41d resulting in highest percentages of both embryogenic callus(81.2%)and regeneration(70.9%),followed by55.0%and45.2%obtained from sub optimal period42~55d,while poor rates(22.5%and16.5%)occurred in prolonged period56~69d.A part of plantlets regenerated from protoplasts were able to root on hormone free1/2MS,whereas rests produced roots after transfer upon the rooting medium1/2MS+IBA0.3mg·L1+0.1%active charcoal.
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