|Table of Contents|

Tissue Culture and Rapid Propagation of Kaempferia galangal L.(PDF)

《北方园艺》[ISSN:1001-0009/CN:23-1247/S]

Issue:
2017年19
Page:
11-15
Research Field:
Publishing date:

Info

Title:
Tissue Culture and Rapid Propagation of Kaempferia galangal L.
Author(s):
LIANG Chunhui1HUANG Min1LI Xiuping1DONG Bin1YAN Xiaodong2
1.Department of Tropical Crops,Guangdong Agriculture Industry Business Polytechnic College,Guangzhou,Guangdong 510507;2.Guangzhou Entry-Exit Inspectional and Quarantine Bureau,Guangzhou,Guangdong 510623
Keywords:
Kaempferia galangal L.adventitious budtissue culture
PACS:
-
DOI:
10.11937/bfyy.20170859
Abstract:
The bud of Kaempferia galangal were was used as the materials,to study the effect of different factors on the disinfection,multiplication,root induction,so as to establish in vitro culture system and provide reference for detoxification.The results showed that the best disinfection method of the bulb explants of Kaempferia galangal was 75% ethanol for 60 seconds,followed by 0.1% HgCl2 8 minutes,the contamination rate was 13.33%,and the survival rate was 86.67%.The effects of hormones on proliferation of adventitious bud were diffferent,the appropriate medium for proliferation was MS+6-BA 2.00 mg?L-1+NAA 0.25 mg?L-1 with the multiplication coefficient of 6.30.The best medium for root induction was 1/2MS+NAA 0.50 mg?L-1 and the number of roots per plantlets was 15.32.

References:

[1]中华人民共和国药典委员会.中国药典(2005年版) [S].一部.北京:化学工业出版社,2005:21.

[2]RUJJANAWATE C,KANJANAPOTHI D,AMOMLERDPISON D,et al.Anti-gastric ulcer effect of Kaemperia parviflora[J].Journal of Ethnopharmacol,2005,102:120-122.
[3]STEVENSON P C,VEITCH C N,SIMMONDS M S J.Polyoxygenated cyclohexane derivatives and other constituents from Kaempferia rotunda L.[J].Phytochemistry,2007,68:1579-1586.
[4]薛颖,村上明,小清水弘一.沙姜中抗促癌有效成分的分离鉴定[J].中国中药杂志,2002,27(7):522.
[5]王锐,何嵋,周云,等.山奈不同溶剂提取物对DPPH自由基的清除作用[J].安徽农业科学,2010,38(29):16232-16233.
[6]何自福,虞皓,李志慧,等.沙姜瘟的发生及田间遮阴防治试验[J].广东农业科学,2005(5):44-45.
[7]王教义.姜脱毒组培技术研究[J].山东农业科学,1999(6):7-9.
[8]邓年方,潘百明.姜的组织培养研究进展[J].安徽农业科学,2009,37(26):12406-12407.[9]佘小漫,何自福.广东沙姜青枯病菌株遗传多样性研究[C].中国植物病理学会,2012年学术年会论文集,2012.
[10]何自福,佘小漫,虞皓,等.沙姜瘟病原菌鉴定[J].农业实验与产业化,2006(4):142-144.[11]文衍堂,郑小波.海南岛广藿香、沙姜青枯病病原菌鉴[J].热带作物学报,1984,5(2):113-117.
[12]高山林.脱毒生姜高产栽培技术[J].农业新技术,2005(1):14-15.
[13]易诚,张天晓,梁称福.黄姜根茎组培快繁技术研究[J].黑龙江农业科学,2008(1):11-13.
[14]黄菊辉.生姜种质资源的离体繁殖和保存[J].中国农业科学,1995,28(2):24-30.
[15]葛胜娟.生姜组培苗的培育及其生产应用[J].中国农学通报,2007,23(5):75-78.
[16]杭玲,黄卓忠,江文,等.生姜组织培养快繁技术研究与应用[J].江苏农业科学,2006(5):125-127.
[17]梁称福,易诚.黄姜组培快繁技术试验研究[J].湖南环境生物职业技术学院学报,2006,12(2):135-138.
[18]张玲,马林,李卫锋.生姜组织培养的快繁技术[J].山地农业生物学报,2003,22(2):173-175.
[19]邱运亮,段鹏慧,赵华.植物组培快繁及时[M].北京:化学工业出版社,2012:58-65.

Memo

Memo:
-
Last Update: 2017-10-11