• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Cloning and nucleotide sequence of ApaLI restriction-modification system from Acetobacter pasteurianus IFO 13753.

作者信息

Suzuki T, Sugimoto E, Tahara Y, Yamada Y

机构信息

United Graduate School of Agricultural Science, Gifu University (Shizuoka University), Japan.

出版信息

Biosci Biotechnol Biochem. 1996 Sep;60(9):1401-5. doi: 10.1271/bbb.60.1401.

DOI:10.1271/bbb.60.1401
PMID:8987585
Abstract

The ApaLI restriction-modification system from Acetobacter pasteurianus IFO 13753 recognizes the nucleotide sequence GTGCAC. The gene coding for the ApaLI methylase (M.ApaLI) was cloned into Escherichia coli DH5 alpha MCR, and the nucleotide sequence of the gene was analyzed. The M.ApaLI gene coded for a protein of 429 amino acid residues (molecular mass, 46,554 daltons). The ApaLI restriction endonuclease (R.ApaLI) gene was analyzed by inverse polymerase chain reaction. The R.ApaLI gene coded for a protein of 375 amino acid residues (molecular mass, 42,143 daltons). The two genes had the same orientation separated by two base pairs. The deduced amino acid sequence of M.ApaLI shows significant similarities to the family of cytosine-5 methylases. However, the deduced amino acid sequence of R.ApaLI did not have as much relatedness in the nucleotide sequence, when compared with those of the other restriction endonucleases already reported.

摘要

相似文献

1
Cloning and nucleotide sequence of ApaLI restriction-modification system from Acetobacter pasteurianus IFO 13753.
Biosci Biotechnol Biochem. 1996 Sep;60(9):1401-5. doi: 10.1271/bbb.60.1401.
2
Cloning and nucleotide sequence of the AgeI methylase gene from Agrobacterium gelatinovorum IAM 12617, a marine bacterium.来自海洋细菌明胶土壤杆菌IAM 12617的AgeI甲基化酶基因的克隆与核苷酸序列分析
Biosci Biotechnol Biochem. 1996 Mar;60(3):444-7. doi: 10.1271/bbb.60.444.
3
Cloning and expression of the ApaLI, NspI, NspHI, SacI, ScaI, and SapI restriction-modification systems in Escherichia coli.ApaLI、NspI、NspHI、SacI、ScaI和SapI限制修饰系统在大肠杆菌中的克隆与表达。
Mol Gen Genet. 1998 Nov;260(2-3):226-31. doi: 10.1007/s004380050890.
4
Cloning and expression of AatII restriction-modification system in Escherichia coli.AatII 限制修饰系统在大肠杆菌中的克隆与表达
Gene. 1997 Jan 31;185(1):105-9. doi: 10.1016/s0378-1119(96)00641-5.
5
Purification, properties and recognition sequence and cleavage site determinations of restriction endonuclease from Acetobacter pasteurianus IFO 13753 (ApaLI).
Agric Biol Chem. 1990 Jul;54(7):1791-6.
6
Cloning and sequence analysis of the StsI restriction-modification gene: presence of homology to FokI restriction-modification enzymes.StsI 限制修饰基因的克隆与序列分析:与 FokI 限制修饰酶存在同源性
Nucleic Acids Res. 1992 Aug 25;20(16):4167-72. doi: 10.1093/nar/20.16.4167.
7
Characterization of the Pac25I restriction-modification genes isolated from the endogenous pRA2 plasmid of Pseudomonas alcaligenes NCIB 9867.从产碱假单胞菌NCIB 9867的内源性pRA2质粒中分离得到的Pac25I限制修饰基因的特性分析
Plasmid. 1998 Nov;40(3):203-13. doi: 10.1006/plas.1998.1365.
8
Cloning and sequence comparison of AvaI and BsoBI restriction-modification systems.AvaI和BsoBI限制-修饰系统的克隆与序列比较
Mol Gen Genet. 1996 Oct 28;252(6):695-9.
9
Genetic organization of the KpnI restriction--modification system.KpnI 限制 - 修饰系统的基因组织
Nucleic Acids Res. 1991 Dec 11;19(23):6505-9. doi: 10.1093/nar/19.23.6505.
10
Cloning and expression of the BalI restriction-modification system.BalI 限制修饰系统的克隆与表达
Nucleic Acids Res. 1996 Jun 15;24(12):2268-70. doi: 10.1093/nar/24.12.2268.