[1]王红玲,孙倩,黄瑞芳.楸叶泡桐杂种无性系9503的组织培养技术研究[J].江苏林业科技,2019,46(02):43-45.[doi:10.3969/j.issn.1001-7380.2019.02.010]
 Wang Hongling,Sun Qian,Huang Ruifang.Research of tissue culture in hybrid clone 9503 of Paulownia catalpifolia[J].Journal of Jiangsu Forestry Science &Technology,2019,46(02):43-45.[doi:10.3969/j.issn.1001-7380.2019.02.010]
点击复制

楸叶泡桐杂种无性系9503的组织培养技术研究()
分享到:

《江苏林业科技》[ISSN:1001-7380/CN:32-1236/S]

卷:
第46卷
期数:
2019年02期
页码:
43-45
栏目:
试验研究
出版日期:
2019-04-30

文章信息/Info

Title:
Research of tissue culture in hybrid clone 9503 of Paulownia catalpifolia
文章编号:
1001-7380(2019)01-0043-03
作者:
王红玲1孙倩2黄瑞芳1
1. 江苏省林业科学研究院,江苏南京211153;
2. 南通农业职业技术学院,江苏南通226007
Author(s):
Wang Hongling1 Sun Qian2 Huang Ruifang1
1.Jiangsu Academy of Forestry, Nanjing 211153, China;
2. Nantong Vocational College of Science & Technology, Nantong 226007, China
关键词:
愈伤组织外植体增殖楸叶泡桐
Keywords:
Callus differentiation Explants Multiflication Paulownia catalpifolia
分类号:
Q943.1;S792.43
DOI:
10.3969/j.issn.1001-7380.2019.02.010
文献标志码:
A
摘要:
以楸叶泡桐和白花泡桐杂交无性系的枝条为外植体,开展了离体芽增殖技术,以及愈伤组织诱导、芽分化和不定芽生根等组织培养技术的研究。结果表明,增殖培养基采用MS+8 mg/L 6-BA +0.3 mg/L NAA ,不定芽的增殖倍数可达到9;利用其叶片进行愈伤组织诱导的最佳培养基为MS+12 mg/L 6-BA +0.4 mg/L NAA,诱导率高达95%;愈伤组织分化的最佳培养基为MS+10 mg/L 6-BA +0.7 mg/L NAA,不定芽生根的最佳培养基为1/2MS+0.5 mg/L IBA+0.3 mg/L NAA,生根率100%。
Abstract:
By using excellent stem segments of the hybrid Clone 9503 of Paulownia fortunei and P. catalpifolia as explants, we studied the tissue culture technology, including callus induction, bud differentiation and bud proliferation. The results showed that the multiplication medium was MS+8 mg/L 6-BA+0.3 mg/L NAA, with 9 of multiplication time. The suitable medium for leaf callus induction was MS+12 mg/L 6-BA+0.4 mg/L NAA, with the induction rate of 95%. The suitable callus differentiation medium was MS+10 mg/L 6-BA+0.7 mg/L NAA. The suitable rooting culture medium was 1/2MS+0.5 mg/L IBA+0.3 mg/L NAA, with the rooting rate of 100%.

参考文献/References:

[1]乔杰,王炜炜,王保平,等.楸叶泡桐嫁接无性系苗期生长优良品种选择[J].东北林业大学学报,2015,43(10):35-41.
[2]蒋建平. 泡桐栽培学[M].北京: 中国林业出版社,1990: 32-33.
[3]李芳东,乔杰,王保平,等.中国泡桐属种质资源图谱[M].北京: 中国林业出版社,2013: 18.
[4]宋玉民, 乔勇进, 焦其宏,等.楸叶桐资源保护与发展途径初探[J].山东林业科技,2000(增刊):50-51.
[5]王安亭, 杨晓娟 , 翟晓巧,等.毛泡桐体细胞胚胎发生及植株再生研究[J].河南农业大学学报,2005,39(1):46-50.
[6]范国强, 翟晓巧, 蒋建平, 等.不同种泡桐叶片愈伤组织诱导及其植株再生[J].林业科学, 2002, 38(1):29-35.
[7]IPEKCI Z, GOZUKIRMIZI N.Direct somatic embryogenesis and synthetic seed production from Paulownia elongate[J]. Plant Cell Reports, 2003, 22(1):16-24.
[8]张变莉,王杨,刘荣宁,等.同源四倍体台湾泡桐体外植株再生系统的建立[J]. 河南农业科学,2015,44(7):119-123.
[9]范国强,翟晓巧,李松林.泡桐愈伤组织再生植株的诱导与培养[J].植物学通报,2002,19(1):92-97.
[10]曲金柱,崔波,马杰,等.白花泡桐叶柄愈伤组织再生植株的诱导与培养[J].信阳师范学院学报(自然科学版), 2006,19(4):407-410.

相似文献/References:

[1]吕运舟,窦全琴,蒋泽平.薄壳山核桃愈伤组织诱导的影响因素[J].江苏林业科技,2015,42(05):29.[doi:10.3969/j.issn.1001-7380.2015.05.009]
 LYU Yun-zhou,DOU Quan-qin,JIANG Ze-ping.Impact factors of the callus inducement and growth of Carya illinoensis in vitro culture[J].Journal of Jiangsu Forestry Science &Technology,2015,42(02):29.[doi:10.3969/j.issn.1001-7380.2015.05.009]
[2]何月秋,黄艾,李波.紫娇花组织培养中愈伤组织的诱导及植株再生[J].江苏林业科技,2015,42(06):19.[doi:doi:10.3969/j.issn.1001-7380.2015.06.005]
 HE Yue-qiu,HUANG Ai,LI Bo.Callus induction and plant regeneration in Tulbaghia violacea in vitro culture[J].Journal of Jiangsu Forestry Science &Technology,2015,42(02):19.[doi:doi:10.3969/j.issn.1001-7380.2015.06.005]
[3]周鹏,张敏*.LED光质对植物组织培养影响研究进展[J].江苏林业科技,2016,43(04):44.[doi:10.3969/j.issn.1001-7380.2016.04.012]
 ZHOU Peng,ZHANG Min*.Application of light-emitting diodes (LEDs) in in vitro plant tissue culture: A review[J].Journal of Jiangsu Forestry Science &Technology,2016,43(02):44.[doi:10.3969/j.issn.1001-7380.2016.04.012]
[4]陈凌艳,陈 拓,吴玉香,等.雷公藤组织培养中嫩叶外植体褐化的控制[J].江苏林业科技,2016,43(06):20.[doi:10.3969/j.issn.1001-7380.2016.06.005]
 CHEN Ling-yan,CHEN Tuo,WU Yu-xiang,et al.Control of browning in the process of callus induction with Tripterygium wilfordii's new leaves[J].Journal of Jiangsu Forestry Science &Technology,2016,43(02):20.[doi:10.3969/j.issn.1001-7380.2016.06.005]
[5]黄益基,吕秀立*,付 瑞,等.金红茵芋离体快速繁殖技术的研究[J].江苏林业科技,2017,44(04):8.[doi:10.3969/j.issn.1001-7380.2017.04.002]
 HUANG Yi-ji,LYU Xiu-li,*,et al.Research of in vitro rapid propagation technique of Skimmia japoniac ‘rnbella’[J].Journal of Jiangsu Forestry Science &Technology,2017,44(02):8.[doi:10.3969/j.issn.1001-7380.2017.04.002]
[6]高亚军,王圳,黄建庭.丝棉木嫩枝扦插育苗试验[J].江苏林业科技,2019,46(01):22.[doi:10.3969/j.issn.1001-7380.2019.01.005]
[7]黄犀,王欢利,严灵君,等.南京椴胚性愈伤组织的诱导[J].江苏林业科技,2020,47(05):18.[doi:10.3969/j.issn.1001-7380.2020.05.004]
[8]吴奇翰.银杏组织培养方案优化研究进展[J].江苏林业科技,2022,49(02):43.[doi:10.3969/j.issn.1001-7380.2022.02.009]
 Wu Qihan.Advance in optimization of the tissue culture formula of Ginkgo biloba L.[J].Journal of Jiangsu Forestry Science &Technology,2022,49(02):43.[doi:10.3969/j.issn.1001-7380.2022.02.009]

备注/Memo

备注/Memo:
收稿日期:2019-02-19;修回日期:2019-03-05
基金项目:江苏省科技支撑(现代农业)项目“适于平原林网更新的泡桐和落羽杉优质材新品种选育”(BE2015371);中央财政林业科技推广示范资金项目“苏北杨树更新良种繁育及高效培育技术推广”(苏[2017]TG03号)
作者简介:王红玲(1982- ),女,江苏宝应人,副研究员,硕士。主要从事林木遗传育种研究。
更新日期/Last Update: 2019-06-11