• 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

大肠杆菌中解除色氨酸酶合成分解代谢物阻遏的突变。远离色氨酸酶基因的突变。

Mutations in Escherichia coli that relieve catabolite repression of tryptophanase synthesis. Mutations distant from the tryptophanase gene.

作者信息

Yudkin M D

出版信息

J Gen Microbiol. 1976 Jan;92(1):125-32. doi: 10.1099/00221287-92-1-125.

DOI:10.1099/00221287-92-1-125
PMID:173793
Abstract

Two mutants are described in which the synthesis of tryptophanase is unusually insensitive to catabolite repression. Neither mutation is linked by transduction to the tryptophane structural gene, neither mutation renders the synthesis of beta-galactosidase insensitive to catabolite repression, and the mutations do not permit tryptophanase to be synthesized in strains deficient in adenyl cyclase. During growth in glucose-minimal medium the mutants maintained a similar intracellular concentration of cyclic AMP to their wild-type parent; but since in the wild type the concentration of cyclic AMP was the same in glycerol-minimal medium as in glucose-minimal medium, it is doubtful whether catabolite repression is mediated by measurable changes in the concentration of this nucleotide.

摘要

本文描述了两个突变体,其中色氨酸酶的合成对分解代谢物阻遏异常不敏感。通过转导,这两个突变均与色氨酸结构基因不连锁,它们均未使β-半乳糖苷酶的合成对分解代谢物阻遏不敏感,并且这些突变不允许在缺乏腺苷酸环化酶的菌株中合成色氨酸酶。在葡萄糖基本培养基中生长期间,这些突变体维持的细胞内环磷酸腺苷(cAMP)浓度与其野生型亲本相似;但由于在野生型中,甘油基本培养基中的cAMP浓度与葡萄糖基本培养基中的相同,因此分解代谢物阻遏是否由该核苷酸浓度的可测量变化介导值得怀疑。

相似文献

1
Mutations in Escherichia coli that relieve catabolite repression of tryptophanase synthesis. Mutations distant from the tryptophanase gene.大肠杆菌中解除色氨酸酶合成分解代谢物阻遏的突变。远离色氨酸酶基因的突变。
J Gen Microbiol. 1976 Jan;92(1):125-32. doi: 10.1099/00221287-92-1-125.
2
Mutations in Escherichia coli that relieve catabolite repression of tryptophanase synthesis. Tryptophanase promoter-like mutations.大肠杆菌中解除色氨酸酶合成分解代谢物阻遏的突变。类色氨酸酶启动子突变。
J Gen Microbiol. 1976 Jan;92(1):133-7. doi: 10.1099/00221287-92-1-133.
3
Unstable mutations that relieve catabolite repression of tryptophanase synthesis by Escherichia coli.可解除大肠杆菌色氨酸酶合成的分解代谢物阻遏作用的不稳定突变。
J Bacteriol. 1977 Apr;130(1):57-61. doi: 10.1128/jb.130.1.57-61.1977.
4
Different cyclic adenosine 3',5'-monophosphate requirements for induction of beta-galactosidase and tryptophanase. Effect of osmotic pressure on intracellular cyclic adenosine 3,5-monophosphate concentrations.诱导β-半乳糖苷酶和色氨酸酶对3',5'-环磷酸腺苷的不同需求。渗透压对细胞内环磷酸腺苷浓度的影响。
Biochemistry. 1975 May 6;14(9):1821-5. doi: 10.1021/bi00680a003.
5
Catabolite modulator factor: a possible mediator of catabolite repression in bacteria.分解代谢调节因子:细菌中分解代谢阻遏的一种可能介导物。
Proc Natl Acad Sci U S A. 1976 Oct;73(10):3476-9. doi: 10.1073/pnas.73.10.3476.
6
On the regulation of adenosine 3', 5'-monophosphate synthesis in bacteria. I. Effect of carbon source variation on cyclic AMP synthesis in Escherichia coli B/r.关于细菌中3',5'-环磷酸腺苷合成的调控。I. 碳源变化对大肠杆菌B/r中环磷酸腺苷合成的影响
Biochim Biophys Acta. 1975 Apr 7;385(2):281-93. doi: 10.1016/0304-4165(75)90356-6.
7
Cell septation and the synthesis of catabolite repressible enzymes in Escherichia coli.大肠杆菌中的细胞分隔与分解代谢物阻遏酶的合成。
Biochem Biophys Res Commun. 1975 Jan 20;62(2):431-8. doi: 10.1016/s0006-291x(75)80157-4.
8
Metabolism of cyclic adenosine 3',5'-monophosphate and induction of tryptophanase in Escherichia coli.大肠杆菌中3',5'-环磷酸腺苷的代谢与色氨酸酶的诱导
J Bacteriol. 1975 Oct;124(1):380-90. doi: 10.1128/jb.124.1.380-390.1975.
9
Effect of cyclic guanosine 3,5-monophosphate on the synthesis of enzymes sensitive to caatabolite repression in intact cells of Escherichia coli.环磷酸鸟苷对大肠杆菌完整细胞中受分解代谢物阻遏敏感的酶合成的影响。
J Bacteriol. 1974 Nov;120(2):980-3. doi: 10.1128/jb.120.2.980-983.1974.
10
Simultaneous induction of three catabolic enzymes in Escherichia coli.大肠杆菌中三种分解代谢酶的同时诱导
Folia Microbiol (Praha). 1980;25(3):201-6. doi: 10.1007/BF02877338.

引用本文的文献

1
Location of the gene for the low-affinity tryptophan-specific permease of Escherichia coli.大肠杆菌低亲和力色氨酸特异性通透酶基因的定位
Biochem J. 1982 May 15;204(2):617-9. doi: 10.1042/bj2040617.
2
Glycerol fermentation in Klebsiella pneumoniae: functions of the coenzyme B12-dependent glycerol and diol dehydratases.肺炎克雷伯菌中的甘油发酵:依赖辅酶B12的甘油和二醇脱水酶的功能
J Bacteriol. 1982 Feb;149(2):413-9. doi: 10.1128/jb.149.2.413-419.1982.
3
Transcription initiation at the tryptophanase promoter of Escherichia coli K-12.
大肠杆菌K-12色氨酸酶启动子处的转录起始
J Bacteriol. 1982 Aug;151(2):942-51. doi: 10.1128/jb.151.2.942-951.1982.
4
Nucleotide sequence of the structural gene for tryptophanase of Escherichia coli K-12.大肠杆菌K-12色氨酸酶结构基因的核苷酸序列。
J Bacteriol. 1981 Sep;147(3):787-96. doi: 10.1128/jb.147.3.787-796.1981.
5
Catabolite repression during single and multiple induction in Escherichia coli.大肠杆菌单次和多次诱导过程中的分解代谢物阻遏
Folia Microbiol (Praha). 1981;26(1):1-7. doi: 10.1007/BF02927215.
6
Identification of a positive regulatory protein in Escherichia coli: the product of the cysB gene.大肠杆菌中一种正向调节蛋白的鉴定:cysB基因的产物。
Mol Gen Genet. 1980 Feb;177(3):535-9. doi: 10.1007/BF00271494.
7
The construction in vitro of transducing derivatives of phage lambda.噬菌体λ转导衍生物的体外构建
Mol Gen Genet. 1976 Jul 23;146(2):199-207. doi: 10.1007/BF00268089.
8
Synthesis of tryptophanase in Escherichia coli: isolation and characterization of a structural-gene mutant and two regulatory mutants.大肠杆菌中色氨酸酶的合成:一个结构基因突变体和两个调节基因突变体的分离与特性分析
Mol Gen Genet. 1978 Sep 20;165(1):95-102. doi: 10.1007/BF00270381.
9
The frequency of P1 transduction of the genes of Escherichia coli as a function of chromosomal position: preferential transduction of the origin of replication.大肠杆菌基因的P1转导频率作为染色体位置的函数:复制起点的优先转导。
Mol Gen Genet. 1977 Oct 20;155(2):197-202. doi: 10.1007/BF00393160.
10
Fine-structure mapping and complementation analysis of the Escherichia coli cysB gene.大肠杆菌cysB基因的精细结构图谱绘制与互补分析
J Bacteriol. 1977 Jul;131(1):49-56. doi: 10.1128/jb.131.1.49-56.1977.