期刊文献+

芽胞杆菌基因敲除技术及其在工农业应用中的研究进展 被引量:3

Research progress on gene knock-out of Bacillus and its industrial and agricultural application
下载PDF
导出
摘要 芽胞杆菌具较强的环境适应能力、抗逆性、分泌能力等优良性状,在工农业生产上具有广阔的应用前景。基因敲除技术是遗传改造芽胞杆菌的重要手段。然而,对于工农业生产中具有许多重要应用价值的芽胞杆菌,目前仍缺乏有效的基因敲除技术。近年来,研究人员在开发适用范围较广泛的芽胞杆菌基因敲除技术方面取得了较显著的进展。该文在简要介绍基因敲除原理的基础上,重点阐述了可在不同芽胞杆菌中操作的基因敲除技术的研究进展,归纳和总结这些方法的局限性,为选择不同基因敲除方法开展芽胞杆菌工农业菌株遗传育种工作提供建议。最后,笔者结合自身的研究工作,展望开发新一代芽胞杆菌基因敲除技术的发展趋势。 The gene knock-out technology is a powerful tool for genetic engineering of Bacillus for the use in industry and agriculture. However,effective gene knock-out technology remains unavailable to many Bacillus strains with important application values. In recent years,researchers made noticeable progresses in developing widely applicable gene knock-out technology for Bacillus. Herein,on the basis of brief introduction of the principle of gene knockout,we mainly describe recent advances in the widely applicable gene knock-out methods for Bacillus and summarize their limitations to provide suggestions for selection of gene knock-out strategies in industrial and agricultural breeding of Bacillus. Finally,based on our previous research,we envision the development of the new gene knock-out technology for Bacillus in the future.
出处 《食品与发酵工业》 CAS CSCD 北大核心 2016年第5期264-271,共8页 Food and Fermentation Industries
基金 浙江省自然科学基金(No.LY16C010003) 杭州市科协人才专项资金(2012院士工作站建设项目)资助
关键词 芽胞杆菌 基因敲除 遗传育种 转化 同源重组 Bacillus gene knock-out genetic breeding transformation homologous recombination
  • 相关文献

参考文献44

  • 1CAPECCHI M R.Altering the genome by homologous recombination[J].Science,1989,244(4 910):1 288-1 292.
  • 2CLAVERYS J P,MARTIN B,POLARD P.The genetic transformation machinery:composition,localization,and mechanism[J].FEMS Microbiology Reviews,2009,33(3):643-656.
  • 3JOHNSTON C,MARTIN B,FICHANT G,et al.Bacterial transformation:distribution,shared mechanisms and divergent control[J].Nature Reviews Microbiology,2014,12(3):181-196.
  • 4SPIZIZEN J.Transformation of biochemically deficient strains of Bacillus subtilis by deoxyribonucleate[J].Proceedings of the National Academy of Sciences of the United States of America,1958,44(10):1 072-1 078.
  • 5VILAS-BOAS L A,VILAS-BOAS G F,SARIDAKIS H O,et al.Survival and conjugation of Bacillus thuringiensis in a soil microcosm[J].FEMS Microbiology Ecology,2000,31(3):255-259.
  • 6RACHINGER M,BAUCH M,STRITTMATTER A,et al.Size unlimited markerless deletions by a transconjugative plasmid-system in Bacillus licheniformis[J].Journal of Biotechnology,2013,167(4):365-369.
  • 7XUE G P,JOHNSON J S,DALRYMPLE B P.High osmolarity improves the electro-transformation efficiency of the gram-positive bacteria Bacillus subtilis and Bacillus licheniformis[J].Journal of Microbiological Methods,1999,34(3):183-191.
  • 8LU Ya-ping,LU Zhao-xin,LV Feng-xia,et al.Study on the electro-transformation conditions of improving transformation efficiency for Bacillus subtilis[J].Letters in Applied Microbiology,2012,55(1):9-14.
  • 9CHANG S,COHEN S N.High frequency transformation of Bacillus subtilis protoplasts by plasmid DNA[J].Genetics and Molecular Research,1979,168(1):111-115.
  • 10ANO T,KOBAYASHI A,SHODA M.Transformation of Bacillus subtilis with the treatment by alkali cations[J].Biotechnology Letters,1990,12(2):99-104.

二级参考文献37

  • 1Yan X, Yu H J, Hong Q, et al. Cre/lox system and PCR-based genome engineering in Bacillus subtilis [ J ] . Appl Environ Microbiol, 2005,74 ( 17 ) : 5556-5562.
  • 2Enyeart PJ, Chirieleison SM, Dao MN, et al. Generalized bacterial genome editing using mobile group II introns and Cre-lox [ J ] . Molecular Systems Biology, 2013, 9 : 685.
  • 3Fabret C, Ehrlich SD, Noirot P. A new mutation delivery system for genome-scale approaches in Bacillus subtilis [ J ] . Molecular Microbiology, 2002, 46 ( 1 ) : 25-36.
  • 4Liu S, Endo K, Ara K, et al. Introduction of marker-free deletions in Bacillus subtilis using the AraR repressor and the ara promoter [ J ] . Microbiology, 2008, 154 ( Pt 9 ) : 2562-2570.
  • 5Keller KL, Bender KS, Wall JD. Development of a markerless genetic exchange system for Desulfavibrio vulgaris hilden borough and its use in generating a strain with increased transformation efficiency [ J ] . Appl Environ Microbiol, 2009, 75 ( 24 ) : 7682-7691.
  • 6Kostner D, Peters B, Mientus M, et al. Importance of codB for new codA-based markerless gene deletion in Gluconobacter strains [ J ] . Appl Microbiol Bioteehnol, 2013, 97 ( 18 ) : $341-8349.
  • 7Blower TR, Salmond GP, Luisi BF. Balancing at survival's edge : the structure and adaptive benefits of prokaryotie toxin-anti-toxin partners [ J ] . Curr Opin Struet Biol, 2011, 21 ( 1 ) : 109-118.
  • 8Yamaguchi Y, Inouye M. Regulation of growth and death in Escherichia coli by toxin-antitoxin systems [ J ] . Nature Reviews Microbiology, 2011, 9 ( 11 ) : 779-790.
  • 9Zhang Y, Zhang J, Hoeflich KP, et al. MazF cleaves cellular mRNAs specifically at ACA to block protein synthesis in Escherichia coli [ J ] . Molecular Cell, 2003, 12 ( 4 ) : 913-923.
  • 10Amitai S, Kolodkin-Gal I, Hananya-Meltabashi M, et al. Escherichia coli MazF leads to the simultaneous selective synthesis of both "death proteins" and "survival proteins" [ J ] . PLOS GENET, 2009, 5 ( 3 ) : e1000390.

共引文献4

同被引文献53

引证文献3

二级引证文献27

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部