以葡萄糖为底物一步法合成γ-氨基丁酸整合型重组钝齿棒杆菌的构建
DOI:
CSTR:
作者:
作者单位:

作者简介:

通讯作者:

中图分类号:

基金项目:

教育部新世纪优秀人才计划(NCET-10-0459);国家“973 项目”(2012CB725202);国家“863 计划”(2011AA02A211);国家自然科学基金(21276110,30970056);中央高校基本科研业务费专项资金(JUSRP51306A);高等学校博士学科点专项科研基金(20110093120001);江苏高校优势学科建设工程项目


One-step fermentation converting glucose in γ-aminobutyric acid by a recombinant Corynebacterium crenatum
Author:
Affiliation:

Fund Project:

Supported by the Program for New Century Excellent Talents in University (NCET-10-0459),by the Key Project of Chinese National Programs for Fundamental Research and Development (2012CB725202),by the National Programs for High Technology Research and Development of China (2011AA02A211),by the National Natural Science Foundation of China (21276110,30970056),by the Fundamental Research Funds for the Central Universities (JUSRP51306A),by the Research Fund for the Doctoral Program of Higher Education of China (20110093120001) and by the Priority Academic Program Development of Jiangsu Higher Education Institutions

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    摘要:【目的】为了构建一株直接利用廉价的葡萄糖合成γ-氨基丁酸的重组钝齿棒杆菌,将来自于植物乳杆菌γ-氨基丁酸合成途径的关键酶谷氨酸脱羧酶基因(lpgad)在产谷氨酸菌株钝齿棒杆菌中进行整合表达,实现葡萄糖到GABA 的一步法生产。【方法】运用PCR 技术扩增得到带有tac启动子的谷氨酸脱羧酶基因tacgad。通过重叠PCR的方法获得钝齿棒杆菌精氨酸合成途径关键酶N-乙酰谷氨酸激酶(NAGK)基因内部缺失型基因ΔargB。利用自杀载体pK18mobsacB构建同源整合载体pK18-ΔargB::tacgad,以ΔargB的上下 游序列为同源臂,通过两次同源重组将tacgad基因整合到钝齿棒杆菌基因组,同时将NAGK 基因argB灭活,利用蔗糖致死基因sacB反向筛选标记筛选得到谷氨酸脱羧酶的重组钝齿棒杆菌C.crenatum ΔargB::tacgad。重组钝齿棒杆菌以葡萄糖为底物进行发酵,测定GABA含量。【结果】重组菌C.crenatum ΔargB::tacgad成功表达谷氨酸脱羧酶,同时阻断了精氨酸合成途径对谷氨酸到GABA代谢途径的竞争,粗酶液基本检测不到NAGK活性,发酵液无精氨酸合成。通过96 h发酵,重组菌可积累约8.28 g/L的GABA。【结论】 本研究通过将谷氨酸脱羧酶基因定向整合到钝齿棒杆菌精氨酸合成途径的关键酶基因argB内部,成功表达谷氨酸脱羧酶的同时阻断竞争途径精氨酸的合成。本研究为实现直接利用葡萄糖合成GABA的一步法生产奠定了基础。

    Abstract:

    Abstract:[Objective]We constructed an integrative recombinant Corynebacterium crenatum that could directly convert glucose in γ-aminobutyric acid (GABA).[Methods] Using overlap PCR,we obtained ΔargB fragment that lacked 491 bp of N-acetylglutamate kinase (NAGK) gene. The glutamate decarboxylase (GAD) gene attached tac promoter was amplified and inserted into ΔargB fragment. Using the upstream and downstream of ΔargB as homologous arms,we constructed pK18-ΔargB:: tacgad which was used for the integration of tacgad gene onto the C.crenatum genome.Through two homologous recombinations,we got an argB blocked strain C.crenatum ΔargB:: tacgad which could successfully express GAD. We also fermented the recombinant strain with glucose as substrate and the production of GABA was detected.[Results]In C.crenatum ΔargB::tacgad,NAGK was totally inactivated and no L-arginine was detected though L-glutamic acid was accumulated. As a result of the efficient expression of GAD,part of L-glutamic acid was transformed into GABA,and the final yield of GABA was about 8. 28 g /L.[Conclusion]We successfully constructed a recombinant strain that could efficiently produce GABA by one-step fermentation from glucose. This research provided a new approach for GABA production.

    参考文献
    相似文献
    引证文献
引用本文

孙红梅,饶志明,李秀鹏,徐美娟,张显,许正宏. 以葡萄糖为底物一步法合成γ-氨基丁酸整合型重组钝齿棒杆菌的构建. 微生物学报, 2013, 53(8): 817-824

复制
分享
文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:2013-01-24
  • 最后修改日期:2013-04-07
  • 录用日期:
  • 在线发布日期: 2013-07-23
  • 出版日期:
文章二维码