Uniform design methods for high efficient micropropagation of Platanthera mandarinorum Rchb. f. var. cornu-bovis (Nevski) Kitag. and Coeloglossum viride (L.) Hartm(基于均匀设计法优化长白舌唇兰和凹舌兰的高效快繁体系)

以长白舌唇兰和凹舌兰的茎尖为外植体,应用均匀设计法筛选最适合于原球茎和类原球茎诱导及类原球茎萌发为完整植株的培养基.结果表明,最适合长白舌唇兰原球茎和类原球茎诱导的培养基为N6 +TDZ 0.05 mg •L-1 + NAA0.01 mg •L-1 +KT0.50 mg •L-1,诱导率为92.5%;最适合凹舌兰原球茎和类原球茎诱导的培养基为N6 + TDZ0.05 mg •L-1 +KT0.50 mg •L-1,诱导率为98%;长白舌唇兰类原球茎萌发为完整植株的最佳培养基为N6+IAA0.01 mg •L-1,萌发率为96%;凹舌兰类原球茎萌发为完整植株的最佳培养基为N6 + IAA0.01...

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Main Authors: GUDi-zhou(顾地周), GAOHan-dong(高捍东)
Format: Article
Language:zho
Published: Zhejiang University Press 2010-03-01
Series:Zhejiang Daxue xuebao. Lixue ban
Subjects:
Online Access:https://doi.org/10.3785/j.issn.1008-9497.2010.02.021
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author GUDi-zhou(顾地周)
GAOHan-dong(高捍东)
author_facet GUDi-zhou(顾地周)
GAOHan-dong(高捍东)
author_sort GUDi-zhou(顾地周)
collection DOAJ
description 以长白舌唇兰和凹舌兰的茎尖为外植体,应用均匀设计法筛选最适合于原球茎和类原球茎诱导及类原球茎萌发为完整植株的培养基.结果表明,最适合长白舌唇兰原球茎和类原球茎诱导的培养基为N6 +TDZ 0.05 mg •L-1 + NAA0.01 mg •L-1 +KT0.50 mg •L-1,诱导率为92.5%;最适合凹舌兰原球茎和类原球茎诱导的培养基为N6 + TDZ0.05 mg •L-1 +KT0.50 mg •L-1,诱导率为98%;长白舌唇兰类原球茎萌发为完整植株的最佳培养基为N6+IAA0.01 mg •L-1,萌发率为96%;凹舌兰类原球茎萌发为完整植株的最佳培养基为N6 + IAA0.01 mg •L-1 +GA30.01 mg •L-1,萌发率为94.5%.以类原球茎的切片为材料进行类原球茎快繁的结果表明,在30~40 d的一个培养周期内,增殖倍数达100以上,成功建立了两种兰的高效快繁体系.同时对不同阶段培养材料的形态结构及超微结构的观察证明了两种兰的类原球茎发生发育过程.
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spelling doaj.art-d8b6822cf1804ab2898265499ba58b462024-03-29T01:58:28ZzhoZhejiang University PressZhejiang Daxue xuebao. Lixue ban1008-94972010-03-0137222122610.3785/j.issn.1008-9497.2010.02.021Uniform design methods for high efficient micropropagation of Platanthera mandarinorum Rchb. f. var. cornu-bovis (Nevski) Kitag. and Coeloglossum viride (L.) Hartm(基于均匀设计法优化长白舌唇兰和凹舌兰的高效快繁体系)GUDi-zhou(顾地周)0GAOHan-dong(高捍东)1 1.Department of Biology, Tonghua Normal University, Tonghua 134002, Jilin Province, China( 1.通化师范学院生物系,吉林 通化 134002) 2.College of Forest Resources and Environment, Nanjing Forestry University, Nanjing 210037, China( 2.南京林业大学森林资源与环境学院,江苏 南京 210037)以长白舌唇兰和凹舌兰的茎尖为外植体,应用均匀设计法筛选最适合于原球茎和类原球茎诱导及类原球茎萌发为完整植株的培养基.结果表明,最适合长白舌唇兰原球茎和类原球茎诱导的培养基为N6 +TDZ 0.05 mg •L-1 + NAA0.01 mg •L-1 +KT0.50 mg •L-1,诱导率为92.5%;最适合凹舌兰原球茎和类原球茎诱导的培养基为N6 + TDZ0.05 mg •L-1 +KT0.50 mg •L-1,诱导率为98%;长白舌唇兰类原球茎萌发为完整植株的最佳培养基为N6+IAA0.01 mg •L-1,萌发率为96%;凹舌兰类原球茎萌发为完整植株的最佳培养基为N6 + IAA0.01 mg •L-1 +GA30.01 mg •L-1,萌发率为94.5%.以类原球茎的切片为材料进行类原球茎快繁的结果表明,在30~40 d的一个培养周期内,增殖倍数达100以上,成功建立了两种兰的高效快繁体系.同时对不同阶段培养材料的形态结构及超微结构的观察证明了两种兰的类原球茎发生发育过程.https://doi.org/10.3785/j.issn.1008-9497.2010.02.021长白舌唇兰凹舌兰均匀设计原球茎类原球茎
spellingShingle GUDi-zhou(顾地周)
GAOHan-dong(高捍东)
Uniform design methods for high efficient micropropagation of Platanthera mandarinorum Rchb. f. var. cornu-bovis (Nevski) Kitag. and Coeloglossum viride (L.) Hartm(基于均匀设计法优化长白舌唇兰和凹舌兰的高效快繁体系)
Zhejiang Daxue xuebao. Lixue ban
长白舌唇兰
凹舌兰
均匀设计
原球茎
类原球茎
title Uniform design methods for high efficient micropropagation of Platanthera mandarinorum Rchb. f. var. cornu-bovis (Nevski) Kitag. and Coeloglossum viride (L.) Hartm(基于均匀设计法优化长白舌唇兰和凹舌兰的高效快繁体系)
title_full Uniform design methods for high efficient micropropagation of Platanthera mandarinorum Rchb. f. var. cornu-bovis (Nevski) Kitag. and Coeloglossum viride (L.) Hartm(基于均匀设计法优化长白舌唇兰和凹舌兰的高效快繁体系)
title_fullStr Uniform design methods for high efficient micropropagation of Platanthera mandarinorum Rchb. f. var. cornu-bovis (Nevski) Kitag. and Coeloglossum viride (L.) Hartm(基于均匀设计法优化长白舌唇兰和凹舌兰的高效快繁体系)
title_full_unstemmed Uniform design methods for high efficient micropropagation of Platanthera mandarinorum Rchb. f. var. cornu-bovis (Nevski) Kitag. and Coeloglossum viride (L.) Hartm(基于均匀设计法优化长白舌唇兰和凹舌兰的高效快繁体系)
title_short Uniform design methods for high efficient micropropagation of Platanthera mandarinorum Rchb. f. var. cornu-bovis (Nevski) Kitag. and Coeloglossum viride (L.) Hartm(基于均匀设计法优化长白舌唇兰和凹舌兰的高效快繁体系)
title_sort uniform design methods for high efficient micropropagation of platanthera mandarinorum rchb f var cornu bovis nevski kitag and coeloglossum viride l hartm 基于均匀设计法优化长白舌唇兰和凹舌兰的高效快繁体系
topic 长白舌唇兰
凹舌兰
均匀设计
原球茎
类原球茎
url https://doi.org/10.3785/j.issn.1008-9497.2010.02.021
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