化工学报 ›› 2014, Vol. 65 ›› Issue (9): 3576-3582.DOI: 10.3969/j.issn.0438-1157.2014.09.036

• 生物化学工程与技术 • 上一篇    下一篇

基于基因组重排技术的多杀菌素高产菌株选育

夏燕春1,2, 王超2, 陈园2, 吴江磊3, 邹球龙2, 张晓琳2, 李春1   

  1. 1 石河子大学化学化工学院/新疆兵团化工绿色过程重点实验室-省部共建国家重点实验室培育基地, 新疆 石河子 832003;
    2 国家粮食局科学研究院, 北京 100037;
    3 武汉轻工大学生物与制药工程学院, 湖北 武汉 430023
  • 收稿日期:2013-12-30 修回日期:2014-03-25 出版日期:2014-09-05 发布日期:2014-09-05
  • 通讯作者: 李春
  • 基金资助:

    粮食公益性行业科研专项(201313002);农业科技成果转化资金项目(SQ2013EC4490009)

Enhanced production of spinosad with strains of Saccharopolyspora spinosa by genome shuffling

XIA Yanchun1,2, WANG Chao2, CHEN Yuan2, WU Jianglei3, ZOU Qiulong2, ZHANG Xiaolin2, LI Chun1   

  1. 1 School of Chemistry and Chemical Engineering/Key Laboratory for Green Process of Chemical Engineering of Xinjiang Bingtuan, Shihezi University, Shihezi 832003, Xinjiang, China;
    2 Academy of State Administration of Grain, Beijing 100037, China;
    3 School of Biology and Pharmaceutical Engineering, Wuhan Polytechnic University, Wuhan 430023, Hubei, China
  • Received:2013-12-30 Revised:2014-03-25 Online:2014-09-05 Published:2014-09-05
  • Supported by:

    supported by Food Public Industry Research (201313002) and Agriculture Science and Technology Achievement Transformation Funds (SQ2013EC4490009).

摘要: 利用课题组前期通过不同物理化学诱变和分子生物学方法获得的8株多杀菌素产生菌为出发菌株,采用96孔板发酵培养结合生物检测的高通量筛选方法,探索了原生质体制备、再生、双亲灭活和原生质体融合等条件,并通过多轮基因组重排获得了多杀菌素高产菌株。结果表明:当菌龄为65 h、溶菌酶浓度为4 mg·ml-1,39℃处理时间20 min时,原生质体的制备率及再生率分别为92.30%和7.66%;60℃恒温水浴90 min以上和紫外照射200 s以上为双亲灭活条件;PEG浓度为50%,在32℃下处理15 min时,原生质体融合率约为1.18%。最终获得1株产量较出发菌株提高了36.07%且遗传稳定的融合株。

关键词: 多杀菌素, 刺糖多孢菌, 原生质体融合, 基因组重排育种

Abstract: In this study, genome shuffling of eight original strains obtained by various methods of chemical and physical mutations was used to achieve rapid improvement of spinosad production. The conditions of preparation, regeneration, parents inactivation and fusion of protoplast of the original strain were investigated. The strain grown for 65 h was treated by 4 mg·ml-1 lysozyme at 39℃ for 20 min, and preparation rate and regeneration rate were 92.30% and 7.66%, respectively. The protoplasts were inactivated by heating at 60℃ for more than 90 min and UV treatment more than 200 s, respectively. The inactivated protoplasts were fused and regenerated in polyethylene glycol (PEG 6000, 50%) for 15 min, and fusion rate was about 1.18%. After three rounds of genome shuffling, a high yielding strain, designated as S.spinosa 3-652, was isolated. The increased yield was about 36.07% higher than that of the original strain. Subculture experiments indicated that the high producers were stable.

Key words: spinosad, Saccharopolyspora spinosa, protoplast fusion, genome shuffling

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