生物技术通报 ›› 2015, Vol. 31 ›› Issue (5): 134-139.doi: 10.13560/j.cnki.biotech.bull.1985.2015.05.021

• 研究报告 • 上一篇    下一篇

小花棘豆Embellisia内生真菌原生质体的制备与再生研究

呼吉雅, 卢萍, 牛艳芳   

  1. (内蒙古师范大学生命科学与技术学院,呼和浩特 010022)
  • 收稿日期:2014-11-24 出版日期:2015-05-18 发布日期:2015-05-18
  • 作者简介:呼吉雅,女,硕士研究生,研究方向:植物及真菌分子生物学;E-mail:hujiya@yeah.net
  • 基金资助:
    国家自然科学基金项目(30860049,31460235)

Preparation and Regeneration of Protoplasts Isolated from Embellisia Fungal Endophyte of Oxytropis glabra

Hu Jiya, Lu Ping, Niu Yanfang   

  1. (College of Life Science and Technology,Inner Mongolia Normal University,Hohhot 010022)
  • Received:2014-11-24 Published:2015-05-18 Online:2015-05-18

摘要: 旨在获得数目多且活力高的小花棘豆Embellisia内生真菌的原生质体,分析和探讨该内生真菌原生质体制备与再生的最佳条件,为后续外源基因转化奠定基础。利用酶解法对制备小花棘豆Embellisia内生真菌菌丝的原生质体,研究酶解液成分、pH、温度、渗透压稳定剂、酶解时间及菌龄对原生质体制备和再生的影响;原生质体在TB3培养基上再生后,研究酶解时间对原生质体再生的影响。结果显示,2.5%(W/V)lysing enzymes、2%(W/V)纤维素酶和3%(W/V)蜗牛酶3种混合酶处理,菌龄为10 d,当酶解温度为30℃、pH5.8、1.2 mol/L MgSO4为渗透压稳定剂,在80 r/min水平摇床酶解8 h时,原生质体浓度较高,达4.42×105个/mL;酶解时间6 h时再生率最高,达46.7%。

关键词: 小花棘豆, 内生真菌, 原生质体, 原生质体制备与再生

Abstract: The aim of this research is to obtain more active and larger amount of protoplasts of Embellisia fungal endophyte from Oxytropis glabra, investigate the optimal conditions of protoplast preparation and regeneration, and lay foundation for setting up later exogenous gene transformation system. The protoplasts are made by enzymes, and the influences on protoplast yield regarding different combined enzymes and their concentration, pH, temperatures, osmotic solutions, enzymolysis time and hyphal culture time were discussed. The protoplasts regenerated on TB3 medium were analyzed for understanding the impacts of different enzymolysis time on the regeneration. The protoplast concentration reached to 4.42×105 /mL when medium mass was hydrolyzed by enzymes consisting of 2.5%(W/V)lysing enzymes, 2%(W/V)cellulose and 3%(W/V)helicase, the culture time was 10 days, the enzymolysis temperature was set to 30℃, the pH was 5.8, the 1.2 mol/L MgSO4 solution was selected as osmotic stabilizer and the cultures were incubated in a flat shaker(80 r/min)for 8 h. The protoplast regeneration rate reached to 46.7% when enzymolysis time was 6 h.

Key words: Oxytropis glabra, fungal endophytes, protoplast, preparation and regeneration