• 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

相似文献

1
Mutation of Escherichia coli capable of expressing gene(s) for beta-lactamase production of Citrobacter freundii.能够表达弗氏柠檬酸杆菌β-内酰胺酶产生基因的大肠杆菌突变体。
Antimicrob Agents Chemother. 1986 Apr;29(4):707-9. doi: 10.1128/AAC.29.4.707.
2
Inducible expression of the chromosomal cdiA from Citrobacter diversus NF85, encoding an ambler class A beta-lactamase, is under similar genetic control to the chromosomal ampC, encoding an ambler class C enzyme, from Citrobacter freundii OS60.来自奇异柠檬酸杆菌NF85的编码安布勒A类β-内酰胺酶的染色体cdiA的可诱导表达,与来自弗氏柠檬酸杆菌OS60的编码安布勒C类酶的染色体ampC受相似的遗传控制。
Microb Drug Resist. 1995 Winter;1(4):285-91. doi: 10.1089/mdr.1995.1.285.
3
Regulatory components in Citrobacter freundii ampC beta-lactamase induction.弗氏柠檬酸杆菌ampCβ-内酰胺酶诱导中的调控成分。
Proc Natl Acad Sci U S A. 1985 Jul;82(14):4620-4. doi: 10.1073/pnas.82.14.4620.
4
Inactivation of the ampD gene causes semiconstitutive overproduction of the inducible Citrobacter freundii beta-lactamase.ampD基因的失活导致可诱导的弗氏柠檬酸杆菌β-内酰胺酶半组成型过量产生。
J Bacteriol. 1987 May;169(5):1923-8. doi: 10.1128/jb.169.5.1923-1928.1987.
5
Cloning and expression of the gene(s) for cephalosporinase production of Citrobacter freundii.弗氏柠檬酸杆菌产头孢菌素酶基因的克隆与表达
Mol Gen Genet. 1983;190(1):85-91. doi: 10.1007/BF00330328.
6
Penicillin-binding protein 2 is required for induction of the Citrobacter freundii class I chromosomal beta-lactamase in Escherichia coli.在大肠杆菌中诱导弗氏柠檬酸杆菌I类染色体β-内酰胺酶需要青霉素结合蛋白2。
Antimicrob Agents Chemother. 1989 Jul;33(7):1116-7. doi: 10.1128/AAC.33.7.1116.
7
Cloning and sequencing of the beta-lactamase gene and surrounding DNA sequences of Citrobacter braakii, Citrobacter murliniae, Citrobacter werkmanii, Escherichia fergusonii and Enterobacter cancerogenus.阴沟肠杆菌、摩氏柠檬酸杆菌、韦氏柠檬酸杆菌、弗格森埃希菌和致癌肠杆菌β-内酰胺酶基因及周边DNA序列的克隆与测序
FEMS Microbiol Lett. 2002 Sep 24;215(1):81-7. doi: 10.1111/j.1574-6968.2002.tb11374.x.
8
Chromosome-encoded narrow-spectrum Ambler class A beta-lactamase GIL-1 from Citrobacter gillenii.来自吉氏柠檬酸杆菌的染色体编码窄谱安布勒A类β-内酰胺酶GIL-1
Antimicrob Agents Chemother. 2007 Apr;51(4):1365-72. doi: 10.1128/AAC.01152-06. Epub 2007 Jan 22.
9
Sequence of the Citrobacter freundii OS60 chromosomal ampC beta-lactamase gene.弗氏柠檬酸杆菌OS60染色体ampCβ-内酰胺酶基因序列
Eur J Biochem. 1986 May 2;156(3):441-5. doi: 10.1111/j.1432-1033.1986.tb09601.x.
10
Substitution of aspartic acid-217 of Citrobacter freundii cephalosporinase and properties of the mutant enzymes.弗氏柠檬酸杆菌头孢菌素酶中天冬氨酸-217的替换及突变酶的性质
FEBS Lett. 1990 May 21;264(2):211-4. doi: 10.1016/0014-5793(90)80250-m.

本文引用的文献

1
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
2
Transduction of linked genetic characters of the host by bacteriophage P1.噬菌体P1对宿主连锁遗传性状的转导
Virology. 1955 Jul;1(2):190-206. doi: 10.1016/0042-6822(55)90016-7.
3
Iodometric assay of penicillinase.青霉素酶的碘量法测定
Nature. 1954 Nov 27;174(4439):1012-3. doi: 10.1038/1741012a0.
4
An infective factor controlling sex compatibility in Bacterium coli.一种控制大肠杆菌性别相容性的感染因子。
J Gen Microbiol. 1953 Feb;8(1):89-103. doi: 10.1099/00221287-8-1-89.
5
Evolutionary divergence of the Citrobacter freundii tryptophan operon regulatory region: comparison with other enteric bacteria.弗氏柠檬酸杆菌色氨酸操纵子调控区的进化分歧:与其他肠道细菌的比较。
J Bacteriol. 1982 Oct;152(1):57-62. doi: 10.1128/jb.152.1.57-62.1982.
6
Comparison of the overlapping frd and ampC operons of Escherichia coli with the corresponding DNA sequences in other gram-negative bacteria.大肠杆菌重叠的frd和ampC操纵子与其他革兰氏阴性菌中相应DNA序列的比较。
J Bacteriol. 1983 Sep;155(3):1297-305. doi: 10.1128/jb.155.3.1297-1305.1983.
7
Cloning and expression of the gene(s) for cephalosporinase production of Citrobacter freundii.弗氏柠檬酸杆菌产头孢菌素酶基因的克隆与表达
Mol Gen Genet. 1983;190(1):85-91. doi: 10.1007/BF00330328.
8
Gene expression of ampicillin resistance transposons, Tn2601 and Tn2602.
Microbiol Immunol. 1980;24(6):479-94. doi: 10.1111/j.1348-0421.1980.tb02852.x.
9
Correction of the nucleotide sequence of the Citrobacter freundii tryptophan operon regulatory region.弗氏柠檬酸杆菌色氨酸操纵子调控区核苷酸序列的校正
J Bacteriol. 1984 Sep;159(3):1063-4. doi: 10.1128/jb.159.3.1063-1064.1984.
10
A model for three-point analysis of random general transduction.随机普遍转导的三点分析模型
Genetics. 1966 Aug;54(2):405-10. doi: 10.1093/genetics/54.2.405.

能够表达弗氏柠檬酸杆菌β-内酰胺酶产生基因的大肠杆菌突变体。

Mutation of Escherichia coli capable of expressing gene(s) for beta-lactamase production of Citrobacter freundii.

作者信息

Murayama S Y, Yamamoto T, Suzuki I, Sawai T

出版信息

Antimicrob Agents Chemother. 1986 Apr;29(4):707-9. doi: 10.1128/AAC.29.4.707.

DOI:10.1128/AAC.29.4.707
PMID:3518627
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC180472/
Abstract

A mutation in a chromosomal gene of Escherichia coli, designated reb, acted in trans to increase the expression of the cloned beta-lactamase gene of Citrobacter freundii. The reb gene was located around 99 min. Deletion mutants in the cloned gene(s) which had lost the regulatory region for induction were also constructed.

摘要

大肠杆菌中一个名为reb的染色体基因突变,可反式作用增加弗氏柠檬酸杆菌克隆的β-内酰胺酶基因的表达。reb基因位于约99分钟处。还构建了克隆基因中缺失诱导调控区的缺失突变体。