|Table of Contents|

Research on in vitro Tissue Culture of Pear Rootstocks OH×F51(PDF)

《北方园艺》[ISSN:1001-0009/CN:23-1247/S]

Issue:
2014年18期
Page:
107-109
Research Field:
Publishing date:

Info

Title:
Research on in vitro Tissue Culture of Pear Rootstocks OH×F51
Author(s):
SONG Jian-kunHUANG Man-naWANG Ran
College of Horticulture,Qingdao Agricultural University,Qingdao,Shandong 266109
Keywords:
pear rootstockOH×F51shoot tipsleavesin vitro tissue culture
PACS:
Q 813.1+2
DOI:
-
Abstract:
Taking pear rootstock OH×F51 as material,the shoot tips tissue culture and leaf callus induction of OH×F51 were studied,in order to gain the optimum way of in vitro culture.The results showed that the suitable medium for shoot tips culture was MS+6-BA 2.0 mg/L+NAA 0.2 mg/L+sugar 30 g/L+agar 6 g/L,with a higher rate of seedling.The optimum medium for leaf callus induction of OH×F51 was NN69+TDZ 3.0 mg/L+IBA 1.0 mg/L+sugar 30 g/L+agar 6 g/L.The placing manner of leaf had a certain influence on the callus induction.The leaves which abaxial surface touched the medium had a higher rate of callus.

References:

[1]Westwood M N,Lombard P B,Bjorstand H O.Performance of Bartlett pear on standard and Old Home×Farmingdale clonal rootstocks[J].J Amer Soc Hort Sci,1976,101(2):161-164.
[2]罗娅,汤浩茹.梨矮化砧木选育与离体繁殖研究进展[J].中国南方果树,2004,33(4):46-49.
[3]贾敬贤.梨砧木育种矮化潜力鉴定研究初报[J].中国果树,1983(2):40-43.
[4]曹霞,柴明.良梨组织培养的回顾与展望[J].中国南方果树,2005,34(4):73-76.
[5]曾斌,李疆,张孝霖,等.库尔勒香梨砧木组织培养[J].经济林研究,2006,24(2):41-43.
[6]李丹丹,王忆,韩振海,等.应用正交设计对组培杜梨快速繁殖的研究[J].北方园艺,2009(1):47-48.
[7]郑亚杰,张茂君,姚寰宇,等.山梨组织培养及快繁技术研究[J].吉林农业科学,2010,35(1):45-46.
[8]韩继成,冯志红,陈霜莹.梨离体叶片诱导不定芽的研究[J].河北果树,1998(2):12.
[9]孙清荣,刘庆忠,赵瑞华.西洋梨叶片直接再生体细胞胚[J].园艺学报,2003,30(1):85-86.

Memo

Memo:
-
Last Update: 2014-11-27