• 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

CcpA转录调节因子在枯草芽孢杆菌碳代谢中的作用。

The role of CcpA transcriptional regulator in carbon metabolism in Bacillus subtilis.

作者信息

Henkin T M

机构信息

Department of Microbiology, Ohio State University, Columbus 43210, USA.

出版信息

FEMS Microbiol Lett. 1996 Jan 1;135(1):9-15. doi: 10.1111/j.1574-6968.1996.tb07959.x.

DOI:10.1111/j.1574-6968.1996.tb07959.x
PMID:8598282
Abstract

The CcpA protein has been identified as a key regulator of carbon metabolism in Bacillus subtilis. CcpA is a DNA binding protein in the LacI/GalR transcriptional repressor family, and genes which respond to CcpA contain common cis-acting target sequences (Ccp boxes). A number of pathways involved in carbon source utilization are repressed by CcpA, while at least one gene which is involved in excretion of excess carbon is activated by CcpA. Genes repressed by CcpA generally contain Ccp boxes within or downstream of the promoter, while ackA, which is activated by CcpA, contains Ccp boxes upstream of the promoter. It therefore appears that CcpA acts globally to direct carbon flow in B. subtilis.

摘要

CcpA蛋白已被确定为枯草芽孢杆菌碳代谢的关键调节因子。CcpA是LacI/GalR转录抑制因子家族中的一种DNA结合蛋白,响应CcpA的基因含有共同的顺式作用靶序列(Ccp框)。许多参与碳源利用的途径受到CcpA的抑制,而至少一个参与过量碳排泄的基因被CcpA激活。被CcpA抑制的基因通常在启动子内部或下游含有Ccp框,而被CcpA激活的ackA基因在启动子上游含有Ccp框。因此,CcpA似乎在全局上指导枯草芽孢杆菌中的碳流。

相似文献

1
The role of CcpA transcriptional regulator in carbon metabolism in Bacillus subtilis.CcpA转录调节因子在枯草芽孢杆菌碳代谢中的作用。
FEMS Microbiol Lett. 1996 Jan 1;135(1):9-15. doi: 10.1111/j.1574-6968.1996.tb07959.x.
2
Transcriptional activation of the Bacillus subtilis ackA promoter requires sequences upstream of the CcpA binding site.枯草芽孢杆菌ackA启动子的转录激活需要CcpA结合位点上游的序列。
J Bacteriol. 2001 Apr;183(7):2389-93. doi: 10.1128/JB.183.7.2389-2393.2001.
3
Transcriptome analysis of temporal regulation of carbon metabolism by CcpA in Bacillus subtilis reveals additional target genes.枯草芽孢杆菌中CcpA对碳代谢时间调控的转录组分析揭示了更多靶基因。
J Mol Microbiol Biotechnol. 2007;12(1-2):82-95. doi: 10.1159/000096463.
4
CcpA causes repression of the phoPR promoter through a novel transcription start site, P(A6).CcpA通过一个新的转录起始位点P(A6)导致phoPR启动子的抑制。
J Bacteriol. 2006 Feb;188(4):1266-78. doi: 10.1128/JB.188.4.1266-1278.2006.
5
Transcriptional activation of the Bacillus subtilis ackA gene requires sequences upstream of the promoter.枯草芽孢杆菌ackA基因的转录激活需要启动子上游的序列。
J Bacteriol. 1998 Nov;180(22):5961-7. doi: 10.1128/JB.180.22.5961-5967.1998.
6
Bacillus subtilis ccpA gene mutants specifically defective in activation of acetoin biosynthesis.枯草芽孢杆菌ccpA基因突变体在激活3-羟基丁酮生物合成方面存在特异性缺陷。
J Bacteriol. 2000 Oct;182(19):5611-4. doi: 10.1128/JB.182.19.5611-5614.2000.
7
Positive regulation of Bacillus subtilis ackA by CodY and CcpA: establishing a potential hierarchy in carbon flow.枯草芽孢杆菌ackA受CodY和CcpA的正向调控:在碳流中建立潜在的层级关系。
Mol Microbiol. 2006 Nov;62(3):811-22. doi: 10.1111/j.1365-2958.2006.05410.x. Epub 2006 Sep 21.
8
Regulators of the Bacillus subtilis cydABCD operon: identification of a negative regulator, CcpA, and a positive regulator, ResD.枯草芽孢杆菌cydABCD操纵子的调控因子:负调控因子CcpA和正调控因子ResD的鉴定
J Bacteriol. 2007 May;189(9):3348-58. doi: 10.1128/JB.00050-07. Epub 2007 Feb 23.
9
CcpA mutants with differential activities in Bacillus subtilis.在枯草芽孢杆菌中具有不同活性的CcpA突变体。
J Mol Microbiol Biotechnol. 2007;12(1-2):96-105. doi: 10.1159/000096464.
10
The regulatory link between carbon and nitrogen metabolism in Bacillus subtilis: regulation of the gltAB operon by the catabolite control protein CcpA.枯草芽孢杆菌中碳代谢与氮代谢之间的调控联系:分解代谢物控制蛋白CcpA对gltAB操纵子的调控
Microbiology (Reading). 2003 Oct;149(Pt 10):3001-3009. doi: 10.1099/mic.0.26479-0.

引用本文的文献

1
Xylose Metabolism and Transport in and Its Application to D-Ribose Production.木糖在[具体内容缺失]中的代谢与转运及其在D-核糖生产中的应用。
J Microbiol Biotechnol. 2025 Apr 24;35:e2504021. doi: 10.4014/jmb.2504.04021.
2
Current models in bacterial hemicellulase-encoding gene regulation.当前细菌半纤维素酶编码基因调控模型。
Appl Microbiol Biotechnol. 2024 Dec;108(1):39. doi: 10.1007/s00253-023-12977-4. Epub 2024 Jan 4.
3
HPr prevents FruR-mediated facilitation of RNA polymerase binding to the fru promoter in Vibrio cholerae.
HPr 可防止 FruR 介导的 RNA 聚合酶与霍乱弧菌 fru 启动子的结合增强。
Nucleic Acids Res. 2023 Jun 23;51(11):5432-5448. doi: 10.1093/nar/gkad220.
4
Carbon catabolite repression on the Rgg2/3 quorum sensing system in Streptococcus pyogenes is mediated by PTS and Mga.碳分解代谢物对酿脓链球菌 Rgg2/3 群体感应系统的阻遏作用是由 PTS 和 Mga 介导的。
Mol Microbiol. 2022 Feb;117(2):525-538. doi: 10.1111/mmi.14866. Epub 2022 Jan 3.
5
Activity of CcpA-Regulated GH18 Family Glycosyl Hydrolases That Contributes to Nutrient Acquisition and Fitness in Enterococcus faecalis.CcpA 调控的 GH18 家族糖苷水解酶的活性有助于粪肠球菌营养物质的获取和适应能力。
Infect Immun. 2021 Oct 15;89(11):e0034321. doi: 10.1128/IAI.00343-21. Epub 2021 Aug 23.
6
Influence of the Alternative Sigma Factor RpoN on Global Gene Expression and Carbon Catabolism in Enterococcus faecalis V583.RpoN 替代σ 因子对粪肠球菌 V583 全局基因表达和碳分解代谢的影响。
mBio. 2021 May 18;12(3):e00380-21. doi: 10.1128/mBio.00380-21.
7
Effects of CcpA against salt stress in Lactiplantibacillus plantarum as assessed by comparative transcriptional analysis.通过比较转录组分析评估CcpA对植物乳杆菌盐胁迫的影响。
Appl Microbiol Biotechnol. 2021 May;105(9):3691-3704. doi: 10.1007/s00253-021-11276-0. Epub 2021 Apr 14.
8
Understanding LrgAB Regulation of Metabolism.了解LrgAB对代谢的调控。
Front Microbiol. 2020 Sep 3;11:2119. doi: 10.3389/fmicb.2020.02119. eCollection 2020.
9
Metabolic control of virulence factor production in Staphylococcus aureus.金黄色葡萄球菌毒力因子产生的代谢控制。
Curr Opin Microbiol. 2020 Jun;55:81-87. doi: 10.1016/j.mib.2020.03.004. Epub 2020 May 7.
10
Systems Biology - A Guide for Understanding and Developing Improved Strains of Lactic Acid Bacteria.系统生物学——理解与开发改良乳酸菌菌株指南
Front Microbiol. 2019 Apr 30;10:876. doi: 10.3389/fmicb.2019.00876. eCollection 2019.