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玻璃化法超低温保存龙眼胚性愈伤组织的初步探讨
引用本文:郭玉琼,赖钟雄,吕柳新.玻璃化法超低温保存龙眼胚性愈伤组织的初步探讨[J].福建农林大学学报(自然科学版),2006,35(3):262-265.
作者姓名:郭玉琼  赖钟雄  吕柳新
作者单位:1. 福建农林大学园艺植物生物工程研究所福建农林大学园艺学院,福建,福州,350002
2. 福建农林大学园艺学院,福建,福州,350002
基金项目:福建省自然科学基金;国家自然科学基金;福建省科技攻关项目
摘    要:采用玻璃化法对不同基因型的龙眼胚性愈伤组织超低温保存进行了初步探讨.将保存一定时间的胚性愈伤组织于常温下用60%玻璃化溶液(2PVS2)装载30 m in,再于0℃下用PVS2溶液平衡60 m in;换新鲜的PVS2溶液,迅速投入液氮中保存;48 h后化冻.结果表明,具有原胚分化的胚性愈伤组织保存后的存活率明显高于普通胚性愈伤组织;40℃温水浴、25℃左右室温和自来水冲洗等3种不同的化冻方式对龙眼胚性愈伤组织玻璃化超低温保存后的存活率具有同样的效果.

关 键 词:龙眼  胚性愈伤组织  超低温保存  玻璃化法
文章编号:1671-5470(2006)03-0262-04
收稿时间:2006-03-20
修稿时间:2006-04-27

Preliminary study on cryopreservation of longan calli by vitrification
GUO Yu-qiong,LAI Zhong-xiong,L Liu-xin.Preliminary study on cryopreservation of longan calli by vitrification[J].Journal of Fujian Agricultural and Forestry University,2006,35(3):262-265.
Authors:GUO Yu-qiong  LAI Zhong-xiong  L Liu-xin
Institution:1. Institute of Horticultural Bioteehnology; 2. College of Hortieuhure, Fujian Agriculture and Forestry University, Fuzhou, Fujian 350002, China
Abstract:The procedure for cryopreservation by vitrification was preliminarily developed in different genotypes of longan calli.The calli were loaded with 60% 2PVS_2 for 30 minutes at room temperature,and then they were exposed to PVS_2 for 60 minutes at the temperature below 0 ℃.Soon afterwards,the calli were put into liquid nitrogen with the new solution of fresh PVS_2,and were thawed 48 hours later.In the experiment,three thawing methods,such as washing by water at 40 ℃,exposing at the room temperature of 25 ℃,and washing by tap water were used to estimate the effects of thawing methods on the survival rate after cryopreservation.The results showed that the relative survival rate of the calli with proembryos was higher than that of the general calli;and that different thawing methods had the same effect on the survival rate of longan calli by cryopreservation.
Keywords:longan  embryogenic callus  cryopreservation  vitrification
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