期刊文献+

基于识别重叠序列特性的限制性内切酶的重组表达策略研究

Recombinant Expression of Restriction Enzymes Based on Recognition of Overlapping Sequence
在线阅读 下载PDF
导出
摘要 甲基转移酶可以保护宿主基因组DNA免受限制性内切酶的消化,根据这一特性,经典的限制性内切酶制备策略是首先通过表达与其配对的甲基转移酶来保护宿主菌株,然后再共表达限制性内切酶,即“一对一”的重组表达模式。作者设计了一个新的策略:通过共表达识别重叠序列的甲基转移酶来保护宿主菌株,以制备限制性内切酶。首先将识别重叠序列的甲基转移酶转入大肠杆菌ER2566,以保护宿主基因组DNA,然后将能识别重叠序列的多个限制性内切酶分别转入该宿主菌株,以进行限制性内切酶的重组表达,即“一对多”的重组表达模式。根据这一方法,利用甲基转移酶M.Esa Dix5 I、M.Alu I和M.Hha I实现了识别重叠序列(TTAA、AGCT和GCGC)的一系列限制性内切酶的重组表达,还利用甲基转移酶M.Alu I成功实现了两个新的R.Sac I同裂酶R.Eco SP4ORF25090P和R.Gma5ORF28P的重组表达。该方法简化了对抵抗限制性内切酶消化的宿主菌株的大量筛选工作,并提供了大规模制备限制性内切酶的能力。这一方法也可用于发现其他微生物中新的同工酶或同裂酶。 Methyltransferases can protect the host genomic DNA from digestion by restriction endonucleases.Based on this property,the classical strategy for preparing restriction endonuclease involves first expressing their paired methyltransferases to protect the host strain,followed by co-expression of the restriction endonuclease,i.e.a'one-to-one'recombinant expression pattern.In this study,we proposed a novel strategy for generating restriction endonucleases by co-expressing a methyltransferase that could recognize overlapping sequences to protect the host strain.Initially,a methyltransferase recognizing the overlapping sequences was transferred into E.coli ER2566 to protect the host genomic DNA.Subsequently,multiple restriction endonucleases capable of recognizing the overlapping sequences were individually transferred into the host strain to achieve the recombinant expression of restriction endonucleases in a'one-to-many'recombinant pattern.According to this approach,a series of restriction endonucleases recognizing overlapping sequences(TTAA,AGCT and GCGC)were successfully achieved using methyltransferases M.EsaDix5 I,M.Alu I and M.Hha I,respectively.Additionally,the recombinant expression of two new R.Sac I isozymes,i.e.,R.EcoSP4ORF25090P and R.Gma5ORF28P,was also successfully achieved through methyltransferase M.Alu I.This approach simplifies the labor-intensive screening process for host strains resistant to restriction endonuclease digestion,while providing the capability for large-scale preparation of restriction endonucleases.Furthermore,this method can be utilized for the discovery of new isoenzymes or isoschizomers in other microorganisms.
作者 王睿君 龚雪梅 王欣竹 叶佳琪 李梦磊 张坤晓 WANG Ruijun;GONG Xuemei;WANG Xinzhu;YE Jiaqi;LI Menglei;ZHANG Kunxiao(School of Pharmacy,Jiangsu Ocean University,Lianyungang 222005,China;Jiangsu Key Laboratory of Marine Pharmaceutical Compound Screening,Jiangsu Ocean University,Lianyungang 222005,China)
出处 《食品与生物技术学报》 CAS CSCD 北大核心 2023年第12期82-89,共8页 Journal of Food Science and Biotechnology
基金 国家自然科学基金青年基金项目(31601191)。
关键词 限制性内切酶 甲基转移酶 重叠序列 同裂酶 同工酶 restriction endonuclease methyltransferase overlapping sequence isoschizomers isoenzymes
作者简介 通信作者:张坤晓(1982—),男,博士,副教授,硕士研究生导师,主要从事生物医药诊断和药物活性物质筛选研究。E-mail:2015000022@jou.edu.cn。
  • 相关文献

参考文献3

二级参考文献42

  • 1毛新,李虹,陈文元.限制性内切酶缓冲液诱导人和家兔染色体显带的研究[J].遗传,1995,17(1):4-6. 被引量:4
  • 2曹新,张思仲.维吾尔、哈萨克及汉族染色体限制酶显带及DA/DAPI二重荧光染色研究[J].中华医学遗传学杂志,1996,13(2):82-84. 被引量:1
  • 3Nieddu M,Pichiri G, Diaz Get al. The organization of classical satellite DNAs in human chromosomes: an approach using Alu I and Taq I restriction endonu- cleases [ J ]. European Journal of Histochemistry, 2009,47 (3) :209-214.
  • 4Mezzanotte R, Rossino R, Nieddu M, et al. The DNA fragments produced by Alu I and BstN I digestion of fixed mouse chromosomes [ J ]. Chromosoma, 1992, 101 (10) :641-644.
  • 5Vinas A, Gomez C, Martinez P, et al. Induction of G- bands on Anguilla anguilla chromosomes by the re- striction endonucleases Hae Ⅲ, Hinf I , and Mse I [ J ]. Cytogenet Cell Genet, 1994,65 ( 1/2 ) : 79-81.
  • 6Mezzanotte R. The selective digestion of polytene and mitotic chromosomes of Drosophila melanogaster by the Alu I and Hae Ⅲ restriction endonucleases [ J]. Chromosoma, 1986,93 ( 3 ) :249-255.
  • 7Miller D, Gosden J, Hastie N, et al. Mechanism of en- donuclease banding of chromosomes [J]. Experimen- tal cell research, 1984,155 ( 1 ) :294-298.
  • 8Sahasrabuddhe C, Pathak S, Hsu T. Responses of mammalian metaphase chromosomes to endonuclease digestion [ J ]. Chromosoma, 1978,69 ( 3 ): 331-338.
  • 9Fareed G, Garon C, Salzman N. Origin and direction of simian virus 40 deoxyribonucleic acid replication [ J ]. Journal of Virology, 1972,10 ( 3 ) :484-491.
  • 10Shepard G, Lawson H, Hawkins G, et al. BsaXI/RFLP analysis of initial or selectively reamplified PCR product is unreliable in detecting the V617F mutation in JAK2 [ JOL]. International Journal of Laboratory Hematology, [2010-12-01 ]. http: //www. mackay- foundation. org/downloads/research2010. pdf.

共引文献1

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