|Table of Contents|

Establishment of Tissue Culture and Rapid Propagation System in Fraxinus velutina

《北方园艺》[ISSN:1001-0009/CN:23-1247/S]

Issue:
2021年19
Page:
78-83
Research Field:
Publishing date:

Info

Title:
Establishment of Tissue Culture and Rapid Propagation System in Fraxinus velutina
Author(s):
XU DingfanLIU YanjunWANG ZhaonanHUANG JunxuanWU ChunxiaLI Jianke
(College of Horticulture and Landscape,Tianjin Agricultural University,Tianjin 300392)
Keywords:
Fraxinus velutinastem segmenttissue culturephytohormonemedium
PACS:
-
DOI:
10.11937/bfyy.20211382
Abstract:
Taking the stem segment of Fraxinus velutina with axillary buds as test material,using tissue culture method,and the tissue culture seedlings were acclimated and transplanted.The effects of different disinfection time on explants,different types and concentrations of plant hormones on axillary bud proliferation,strong seedling culture and rooting culture were studied,in order to establish a perfect tissue culture rapid propagation system of Fraxinus velutina,and provide a reference for fine clone breeding and industrialized production of Fraxinus velutina.The results showed that,the optimal explant disinfection treatment was 70% alcohol disinfection for 30 seconds+2% sodium hypochlorite disinfection for 10 minutes,the pollution rate was only 4.44%,the highest survival rate was 90.00%,the mortality rate was 5.56%;the optimal proliferation medium was MS+0.5 mg?L-1 BA+1.0 mg?L-1 IAA,the proliferation coefficient was 5.52;the optimal seedling culture medium was MS+0.5 mg?L-1 IAA,the average seedling height was 5.83 cm;the optimal rooting medium was 1/2MS+0.5 mg?L-1 NAA,the rooting rate was 98.89%,the average number of roots per plant was 5.62;after rooting,the seedlings were domesticated under natural light for one week,and transplanted into peat∶vermiculite∶perlite=1∶1∶1 matrix,the survival rate was more than 90%.

References:

[1]燕丽萍,刘翠兰,李丽,等.耐盐绒毛白蜡特异性SCAR分子标记的鉴定[J].西北植物学报,2014,34(4):671-675.[2]李田,彭振英,范仲学,等.绒毛白蜡2个MYB转录因子的活性鉴定及其表达分析[J].江西农业大学学报,2013,35(5):970-976.[3]王因花,燕丽萍,李庆华,等.绒毛白蜡新品种‘盐蜡’[J].园艺学报,2020,47(S2):3132-3133.[4]任飞,刘翠兰,燕丽萍,等.绒毛白蜡新品种‘紫箭’[J].园艺学报,2020,47(S2):3134-3135.[5]刘翠兰.绒毛白蜡新品种华雄[J].农村百事通,2019(15):34.[6]徐明广,龙庄如,梁玉堂.绒毛白蜡微体快速繁殖的研究[J].山东农业大学学报,1989(3):61-65.[7]宗莉.绒毛白蜡再生体系的建立及BADH基因转化的研究[D].兰州:甘肃农业大学,2003.[8]夏阳,梁慧敏,孙仲序,等.绒毛白蜡组织培育技术体系的建立[C].北京:中国科协2003年学术年会,2003.[9]陈之群,刘志敏.绒毛白蜡茎段的组织培养及植株再生[J].安徽农业科学,2006(3):472-473.[10]王因花,燕丽萍,孔雨光,等.绒毛白蜡组培快繁研究[J].中国农学通报,2019,35(14):41-46.[11]燕丽萍,李丽,刘翠兰,等.绒毛白蜡体胚诱导和植株再生[J].植物学报,2016,51(6):807-816.[12]咸洋,韩彪,穆艳娟,等.绒毛白蜡组织培养研究[J].安徽农学通报,2020,26(8):16-17,32.[13]许丁帆,刘艳军,黄俊轩,等.一种组培苗移栽保湿装置[P].中国:CN211268048U,2020-08-18.[14]饶丹丹,王湘莹,蔡能,等.紫叶紫薇良种组培快繁研究[J].中南林业科技大学学报,2020,40(12):75-82.[15]王晓明.灰毡毛忍冬新品种ISSR分子标记及组织培养的研究[D].长沙:中南林业科技大学,2012.[16]王胤,姚瑞玲,李慧娟,等.基于外植体生理复幼的马尾松茎段芽无菌离体培养[J].植物生理学报,2019,55(9):1375-1384.[17]刘瑞,张嘉仪,葛超奇,等.2个北美冬青新品种组培快繁高效再生技术体系的建立[J].植物研究,2021,41(2):221-231.[18]宁苓.绒毛白蜡组培快繁技术研究[J].辽宁林业科技,2018(4):36-37.[19]王磊,李淑娟,徐云刚,等.绒毛白蜡成熟胚和茎段培养繁殖体系的建立[J].林业科技,2008(3):1-3.[20]李淑娟.绒毛白蜡引种及白蜡属内种间杂交育种研究[D].哈尔滨:东北林业大学,2009.[21]陈琴,黄开勇,蓝肖,等.我国杉木组织培养技术研究进展[J].世界林业研究,2012,25(6):58-63.[22]刘小夫.5个丰花月季优良品系的组培快繁技术研究[D].哈尔滨:东北农业大学,2013.

Memo

Memo:
-
Last Update: 2022-01-04