• 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K-12腺苷酸环化酶缺陷菌株中乙酰羟酸合酶活性的调控

Regulation of acetohydroxy acid synthase activities in adenyl cyclase-deficient strains of Escherichia coli K-12.

作者信息

Williams A L

出版信息

Mol Gen Genet. 1983;191(3):353-7. doi: 10.1007/BF00425745.

DOI:10.1007/BF00425745
PMID:6314089
Abstract

Previous findings suggested that cyclic AMP was involved in the regulation of ilvB(AHASI) only and that ilvG (AHASII) and ilvHI (AHASIII) were not controlled by this nucleotide. In this study, derepression patterns of total AHAS activities (ilvB and ilvHI) in adenyl cyclase-negative strains (i.e. cya-) were substantially reduced as contrasted with AHAS activity observed for cya+ strains. Further, the parental strains (cya+) consistently exhibited higher levels of AHAS activity than mutant strains (cya-) during carbon and energy downshifts. Other data suggested that the valine derepression signal could not override the necessity for cya gene product to yield maximal derepression of AHAS gene activities. Cyclic AMP stimulated AHAS gene activities under both in vivo and in vitro assay conditions. Thus, these data provide evidence for an absolute requirement of cAMP for maximal expression of the genes encoding for AHAS activities of E. coli K-12.

摘要

先前的研究结果表明,环磷酸腺苷(cAMP)仅参与对ilvB(AHASI)的调控,而ilvG(AHASII)和ilvHI(AHASIII)不受该核苷酸的控制。在本研究中,与cya+菌株中观察到的AHAS活性相比,腺苷酸环化酶阴性菌株(即cya-)中总AHAS活性(ilvB和ilvHI)的去阻遏模式大幅降低。此外,在碳源和能源下降期间,亲本菌株(cya+)始终表现出比突变菌株(cya-)更高水平的AHAS活性。其他数据表明,缬氨酸去阻遏信号无法超越cya基因产物对AHAS基因活性产生最大去阻遏的必要性。在体内和体外测定条件下,环磷酸腺苷均刺激AHAS基因活性。因此,这些数据为环磷酸腺苷对大肠杆菌K-12中编码AHAS活性的基因的最大表达的绝对需求提供了证据。

相似文献

1
Regulation of acetohydroxy acid synthase activities in adenyl cyclase-deficient strains of Escherichia coli K-12.大肠杆菌K-12腺苷酸环化酶缺陷菌株中乙酰羟酸合酶活性的调控
Mol Gen Genet. 1983;191(3):353-7. doi: 10.1007/BF00425745.
2
Regulation of cyclic AMP of the ilvB-encoded biosynthetic acetohydroxy acid synthase in Escherichia coli K-12.大肠杆菌K-12中ilvB编码的生物合成乙酰羟酸合酶的环磷酸腺苷调节
Mol Gen Genet. 1980 Apr;178(1):179-83. doi: 10.1007/BF00267227.
3
Regulation of expression of the ilvB operon in Salmonella typhimurium.鼠伤寒沙门氏菌中ilvB操纵子表达的调控
J Bacteriol. 1984 Dec;160(3):833-41. doi: 10.1128/jb.160.3.833-841.1984.
4
Acetohydroxy acid synthase I, a required enzyme for isoleucine and valine biosynthesis in Escherichia coli K-12 during growth on acetate as the sole carbon source.乙酰羟酸合酶I,是大肠杆菌K-12在以乙酸盐作为唯一碳源生长期间异亮氨酸和缬氨酸生物合成所需的一种酶。
J Bacteriol. 1986 Feb;165(2):453-60. doi: 10.1128/jb.165.2.453-460.1986.
5
Growth inhibition of Escherichia coli K-12 by L-valine: a consequence of a regulatory pattern.L-缬氨酸对大肠杆菌K-12的生长抑制作用:一种调控模式的结果
Mol Gen Genet. 1977 Nov 4;156(1):1-7. doi: 10.1007/BF00272245.
6
Regulation of acetohydroxy acid synthase activities in Escherichia coli K-12 by small metabolites.
Biochim Biophys Acta. 1986 Feb 24;866(1):15-8. doi: 10.1016/0167-4781(86)90094-1.
7
Cyclic AMP can replace the relA-dependent requirement for derepression of acetohydroxy acid synthase in E. coli K-12.
Cell. 1977 Dec;12(4):1121-6. doi: 10.1016/0092-8674(77)90174-x.
8
Reduced expression of the isoleucine and valine enzymes in integration host factor mutants of Escherichia coli.大肠杆菌整合宿主因子突变体中异亮氨酸和缬氨酸酶的表达降低。
J Mol Biol. 1984 Feb 5;172(4):573-9. doi: 10.1016/s0022-2836(84)80024-8.
9
Starvation for ilvB operon leader amino acids other than leucine or valine does not increase acetohydroxy acid synthase activity in Escherichia coli.除亮氨酸或缬氨酸外,ilvB操纵子前导氨基酸的饥饿状态不会增加大肠杆菌中乙酰羟酸合酶的活性。
J Bacteriol. 1985 Jun;162(3):1314-6. doi: 10.1128/jb.162.3.1314-1316.1985.
10
The ilvG gene is expressed in Escherichia coli K-12.ilvG基因在大肠杆菌K-12中表达。
Gene. 1980 Dec;12(1-2):165-70. doi: 10.1016/0378-1119(80)90028-1.

引用本文的文献

1
CsiR-Mediated Signal Transduction Pathway in Response to Low Iron Conditions Promotes Escherichia coli K1 Invasion and Penetration of the Blood-Brain Barrier.CsiR 介导的低铁应答信号转导通路促进大肠杆菌 K1 侵袭和穿透血脑屏障。
J Infect Dis. 2024 Oct 16;230(4):e807-e817. doi: 10.1093/infdis/jiae157.
2
Cyclic AMP in prokaryotes.原核生物中的环磷酸腺苷
Microbiol Rev. 1992 Mar;56(1):100-22. doi: 10.1128/mr.56.1.100-122.1992.

本文引用的文献

1
Mutants of Escherichia coli requiring methionine or vitamin B12.需要甲硫氨酸或维生素B12的大肠杆菌突变体。
J Bacteriol. 1950 Jul;60(1):17-28. doi: 10.1128/jb.60.1.17-28.1950.
2
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.
3
Molecular basis of valine resistance in Escherichia coli K-12.大肠杆菌K-12中缬氨酸抗性的分子基础。
Proc Natl Acad Sci U S A. 1981 Feb;78(2):922-5. doi: 10.1073/pnas.78.2.922.
4
A new map location for the ilvB locus of Escherichia coli.大肠杆菌ilvB基因座的一个新图谱定位。
Genetics. 1980 Sep;96(1):59-77. doi: 10.1093/genetics/96.1.59.
5
Linkage map of Escherichia coli K-12, edition 6.大肠杆菌K-12连锁图谱,第6版。
Microbiol Rev. 1980 Mar;44(1):1-56. doi: 10.1128/mr.44.1.1-56.1980.
6
Nucleotide sequence of ilvGEDA operon attenuator region of Escherichia coli.大肠杆菌ilvGEDA操纵子衰减子区域的核苷酸序列。
Proc Natl Acad Sci U S A. 1980 Apr;77(4):1823-7. doi: 10.1073/pnas.77.4.1823.
7
Nucleotide sequence of the argF regulatory region of Escherichia coli K-12.大肠杆菌K-12的argF调控区的核苷酸序列。
Gene. 1981 Dec;16(1-3):119-32. doi: 10.1016/0378-1119(81)90068-8.
8
Regulation of cyclic AMP of the ilvB-encoded biosynthetic acetohydroxy acid synthase in Escherichia coli K-12.大肠杆菌K-12中ilvB编码的生物合成乙酰羟酸合酶的环磷酸腺苷调节
Mol Gen Genet. 1980 Apr;178(1):179-83. doi: 10.1007/BF00267227.
9
Multivalent translational control of transcription termination at attenuator of ilvGEDA operon of Escherichia coli K-12.大肠杆菌K-12 ilvGEDA操纵子弱化子处转录终止的多价翻译控制
Proc Natl Acad Sci U S A. 1980 Apr;77(4):1862-6. doi: 10.1073/pnas.77.4.1862.
10
In vitro synthesis of protein in microbial systems.微生物系统中蛋白质的体外合成。
Annu Rev Genet. 1973;7:267-87. doi: 10.1146/annurev.ge.07.120173.001411.