The embryogenic callus induction and shoot regeneration were studied systematically in elite clone GL9 of Eucalyptus cultivated widely in south China.We investigated TDZ 0.02-0.05 mg·L-1 was the proper concentrat...The embryogenic callus induction and shoot regeneration were studied systematically in elite clone GL9 of Eucalyptus cultivated widely in south China.We investigated TDZ 0.02-0.05 mg·L-1 was the proper concentration.The callus induction rate was 92.9%—100%.When TDZ concentration was higher than 0.1 mg·L-1,the axillary bud germination was completely inhibited.TDZ 0.02 mg·L-1 with combinations of CoCl2 0.125 mg·L-1 could induct the embryogenic callus.The direct regeneration rate was 13.39%±1.03%,and with combinations of NAA 0.1mg·L-1 could not differentiate directly from callus,but higher regeneration rate(20.2%±13.3%) could be obtained by transferring callus onto regeneration medium.The size of callus can increase to 1.4 fold of its original size in the first subculture in modified MS+TDZ 0.02 mg·L-1 +NAA 0.1 mg·L-1medium and the average number of deep-pink-coloured masses of embryogenic cells on each callus was 8.4.In the second and third subculture,callus stopped growing further and the number of masses of embryogenic cells decreased gradually.Regeneration system could lay a good foundation for further transformation research.展开更多
在无菌条件下培养仙客来种子,并以无菌萌发植株的子叶节、子叶、叶片及叶柄为外植体进行芽分化诱导。试验结果表明,不同浓度TDZ对各外植体的诱导效果不同,用子叶节、子叶、叶片及叶柄均可诱导出再生芽,但以叶片为材料的诱导效果最佳,其...在无菌条件下培养仙客来种子,并以无菌萌发植株的子叶节、子叶、叶片及叶柄为外植体进行芽分化诱导。试验结果表明,不同浓度TDZ对各外植体的诱导效果不同,用子叶节、子叶、叶片及叶柄均可诱导出再生芽,但以叶片为材料的诱导效果最佳,其中1.0 m g/L TDZ对叶片再生芽的诱导效果最好,而子叶以0.5 m g/LTDZ、子叶节和叶柄以0.2 m g/L TDZ诱导再生芽的效果较好。展开更多
文摘The embryogenic callus induction and shoot regeneration were studied systematically in elite clone GL9 of Eucalyptus cultivated widely in south China.We investigated TDZ 0.02-0.05 mg·L-1 was the proper concentration.The callus induction rate was 92.9%—100%.When TDZ concentration was higher than 0.1 mg·L-1,the axillary bud germination was completely inhibited.TDZ 0.02 mg·L-1 with combinations of CoCl2 0.125 mg·L-1 could induct the embryogenic callus.The direct regeneration rate was 13.39%±1.03%,and with combinations of NAA 0.1mg·L-1 could not differentiate directly from callus,but higher regeneration rate(20.2%±13.3%) could be obtained by transferring callus onto regeneration medium.The size of callus can increase to 1.4 fold of its original size in the first subculture in modified MS+TDZ 0.02 mg·L-1 +NAA 0.1 mg·L-1medium and the average number of deep-pink-coloured masses of embryogenic cells on each callus was 8.4.In the second and third subculture,callus stopped growing further and the number of masses of embryogenic cells decreased gradually.Regeneration system could lay a good foundation for further transformation research.
文摘在无菌条件下培养仙客来种子,并以无菌萌发植株的子叶节、子叶、叶片及叶柄为外植体进行芽分化诱导。试验结果表明,不同浓度TDZ对各外植体的诱导效果不同,用子叶节、子叶、叶片及叶柄均可诱导出再生芽,但以叶片为材料的诱导效果最佳,其中1.0 m g/L TDZ对叶片再生芽的诱导效果最好,而子叶以0.5 m g/LTDZ、子叶节和叶柄以0.2 m g/L TDZ诱导再生芽的效果较好。
