• 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

碳代谢调节大肠杆菌中pfl(丙酮酸甲酸裂解酶)基因的表达。

Carbon metabolism regulates expression of the pfl (pyruvate formate-lyase) gene in Escherichia coli.

作者信息

Rasmussen L J, Møller P L, Atlung T

机构信息

Department of Microbiology, Technical University of Denmark, Copenhagen.

出版信息

J Bacteriol. 1991 Oct;173(20):6390-7. doi: 10.1128/jb.173.20.6390-6397.1991.

DOI:10.1128/jb.173.20.6390-6397.1991
PMID:1917868
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC208971/
Abstract

The anaerobic expression of pfl is reduced both in a strain mutated in the pgi gene and in a pfkA pfkB double mutant strain when cells are grown in medium supplemented with glucose. When cells are grown in medium supplemented with either fructose or pyruvate, no reduction is observed in these strains. The amount of pyruvate in the cells may be responsible for the reduced expression of pfl in the strains mutated in the genes encoding the glycolytic enzymes. Because of the lowered oxygen concentration in the medium, the expression of pfl is induced when an exponentially growing culture enters the stationary phase. This induction is increased when the Casamino Acid concentration is raised 10-fold or when the medium is supplemented with NaCl. Superhelicity of DNA is decreased in a pgi mutant strain grown in medium supplemented with glucose. The superhelicity is also changed, but the opposite way, in a wild-type strain grown in medium supplemented with Casamino Acids at a high concentration or 0.3 M sodium chloride. Our data show that changes in superhelicity do not affect the aerobic expression of pfl but might be important for the anaerobic induction of pfl.

摘要

当细胞在添加葡萄糖的培养基中生长时,pgi基因突变菌株和pfkA pfkB双突变菌株中pfl的厌氧表达均降低。当细胞在添加果糖或丙酮酸的培养基中生长时,在这些菌株中未观察到表达降低。细胞中丙酮酸的量可能是编码糖酵解酶的基因突变菌株中pfl表达降低的原因。由于培养基中氧浓度降低,当指数生长的培养物进入稳定期时,pfl的表达被诱导。当酪蛋白氨基酸浓度提高10倍或培养基添加NaCl时,这种诱导作用增强。在添加葡萄糖的培养基中生长的pgi突变菌株中,DNA的超螺旋性降低。在添加高浓度酪蛋白氨基酸或0.3M氯化钠的培养基中生长的野生型菌株中,超螺旋性也发生变化,但方向相反。我们的数据表明,超螺旋性的变化不影响pfl的需氧表达,但可能对pfl的厌氧诱导很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f240/208971/64c5d6403eaa/jbacter01038-0092-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f240/208971/64c5d6403eaa/jbacter01038-0092-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f240/208971/64c5d6403eaa/jbacter01038-0092-a.jpg

相似文献

1
Carbon metabolism regulates expression of the pfl (pyruvate formate-lyase) gene in Escherichia coli.碳代谢调节大肠杆菌中pfl(丙酮酸甲酸裂解酶)基因的表达。
J Bacteriol. 1991 Oct;173(20):6390-7. doi: 10.1128/jb.173.20.6390-6397.1991.
2
Integration host factor is required for anaerobic pyruvate induction of pfl operon expression in Escherichia coli.整合宿主因子是大肠杆菌中厌氧丙酮酸诱导pfl操纵子表达所必需的。
J Bacteriol. 1993 Sep;175(18):5769-77. doi: 10.1128/jb.175.18.5769-5777.1993.
3
Transcription of pfl is regulated by anaerobiosis, catabolite repression, pyruvate, and oxrA: pfl::Mu dA operon fusions of Salmonella typhimurium.pfl的转录受厌氧、分解代谢物阻遏、丙酮酸和oxrA调控:鼠伤寒沙门氏菌的pfl::Mu dA操纵子融合体
J Bacteriol. 1989 Sep;171(9):4900-5. doi: 10.1128/jb.171.9.4900-4905.1989.
4
Anaerobic regulation of pyruvate formate-lyase from Escherichia coli K-12.大肠杆菌K-12丙酮酸甲酸裂解酶的厌氧调控
J Bacteriol. 1988 Nov;170(11):5330-6. doi: 10.1128/jb.170.11.5330-5336.1988.
5
Expression of the pfl gene and resulting metabolite flux distribution in nuo and ackA-pta E. coli mutant strains.pfl基因在大肠杆菌nuo和ackA-pta突变菌株中的表达及由此产生的代谢物通量分布。
Biotechnol Prog. 2006 May-Jun;22(3):898-902. doi: 10.1021/bp050326h.
6
Isolation and characterization of hypophosphite--resistant mutants of Escherichia coli: identification of the FocA protein, encoded by the pfl operon, as a putative formate transporter.大肠杆菌次磷酸盐抗性突变体的分离与鉴定:由pfl操纵子编码的FocA蛋白被鉴定为一种假定的甲酸转运蛋白。
Mol Microbiol. 1994 Mar;11(5):965-82. doi: 10.1111/j.1365-2958.1994.tb00375.x.
7
A radical-chemical route to acetyl-CoA: the anaerobically induced pyruvate formate-lyase system of Escherichia coli.通向乙酰辅酶A的自由基化学途径:大肠杆菌厌氧诱导的丙酮酸甲酸裂解酶系统
FEMS Microbiol Rev. 1990 Aug;6(4):383-98. doi: 10.1111/j.1574-6968.1990.tb04108.x.
8
Anaerobic induction of pyruvate formate-lyase gene expression is mediated by the ArcA and FNR proteins.丙酮酸甲酸裂解酶基因表达的厌氧诱导由ArcA和FNR蛋白介导。
J Bacteriol. 1992 Jun;174(11):3474-8. doi: 10.1128/jb.174.11.3474-3478.1992.
9
The effect of pfl gene knockout on the metabolism for optically pure D-lactate production by Escherichia coli.pfl基因敲除对大肠杆菌生产光学纯D-乳酸代谢的影响。
Appl Microbiol Biotechnol. 2004 Apr;64(3):367-75. doi: 10.1007/s00253-003-1499-9. Epub 2003 Dec 12.
10
Structure and transcriptional regulation of the gene encoding pyruvate formate-lyase of a ruminal bacterium, Streptococcus bovis.瘤胃细菌牛链球菌丙酮酸甲酸裂解酶编码基因的结构与转录调控
Microbiology (Reading). 1999 Jan;145 ( Pt 1):151-157. doi: 10.1099/13500872-145-1-151.

引用本文的文献

1
Impaired glucose metabolism by deleting the operon of hydrogenase 2 in Escherichia coli.在大肠杆菌中通过删除氢化酶 2 的操纵子来影响葡萄糖代谢。
Arch Microbiol. 2022 Sep 17;204(10):627. doi: 10.1007/s00203-022-03245-6.
2
Proteomic and metabolomic analysis of the cellular biomarkers related to inhibitors tolerance in ZM4.与ZM4中抑制剂耐受性相关的细胞生物标志物的蛋白质组学和代谢组学分析
Biotechnol Biofuels. 2018 Oct 16;11:283. doi: 10.1186/s13068-018-1287-5. eCollection 2018.
3
Comparative Proteomic Analysis of Differential Proteins in Response to Aqueous Extract of Quercus infectoria Gall in Methicillin-Resistant Staphylococcus aureus.

本文引用的文献

1
Anaerobic and leucine-dependent expression of a peptide transport gene in Salmonella typhimurium.鼠伤寒沙门氏菌中一种肽转运基因的厌氧和亮氨酸依赖性表达。
J Bacteriol. 1984 Oct;160(1):131-6. doi: 10.1128/jb.160.1.131-136.1984.
2
Cyclic AMP receptor protein: role in transcription activation.环磷酸腺苷受体蛋白:在转录激活中的作用。
Science. 1984 May 25;224(4651):831-8. doi: 10.1126/science.6372090.
3
Use of phi(glp-lac) in studies of respiratory regulation of the Escherichia coli anaerobic sn-glycerol-3-phosphate dehydrogenase genes (glpAB).
耐甲氧西林金黄色葡萄球菌对没食子虫瘿水提取物反应中差异蛋白的比较蛋白质组学分析
Int J Proteomics. 2016;2016:4029172. doi: 10.1155/2016/4029172. Epub 2016 Sep 5.
4
Metabolomic and transcriptomic stress response of Escherichia coli.大肠杆菌的代谢组学和转录组学应激反应。
Mol Syst Biol. 2010 May 11;6:364. doi: 10.1038/msb.2010.18.
5
The lysine decarboxylase CadA protects Escherichia coli starved of phosphate against fermentation acids.赖氨酸脱羧酶CadA可保护缺乏磷酸盐的大肠杆菌免受发酵酸的侵害。
J Bacteriol. 2007 Mar;189(6):2249-61. doi: 10.1128/JB.01306-06. Epub 2007 Jan 5.
6
The Escherichia coli tppB (ydgR) gene represents a new class of OmpR-regulated genes.大肠杆菌tppB(ydgR)基因代表了一类新的受OmpR调控的基因。
J Bacteriol. 2004 Jun;186(12):4019-24. doi: 10.1128/JB.186.12.4019-4024.2004.
7
FNR-mediated oxygen-responsive regulation of the nrdDG operon of Escherichia coli.大肠杆菌nrdDG操纵子的FNR介导的氧响应调控
J Bacteriol. 2003 Sep;185(17):5310-3. doi: 10.1128/JB.185.17.5310-5313.2003.
8
Effect of different concentrations of H-NS protein on chromosome replication and the cell cycle in Escherichia coli.不同浓度的H-NS蛋白对大肠杆菌染色体复制及细胞周期的影响
J Bacteriol. 2002 Apr;184(7):1843-50. doi: 10.1128/JB.184.7.1843-1850.2002.
9
Fur positive regulation of iron superoxide dismutase in Escherichia coli: functional analysis of the sodB promoter.大肠杆菌中铁超氧化物歧化酶的Fur正调控:sodB启动子的功能分析
J Bacteriol. 2000 Jul;182(13):3802-8. doi: 10.1128/JB.182.13.3802-3808.2000.
10
DnaA boxes are important elements in setting the initiation mass of Escherichia coli.DnaA框是设定大肠杆菌起始质量的重要元件。
J Bacteriol. 1999 May;181(9):2683-8. doi: 10.1128/JB.181.9.2683-2688.1999.
φ(glp-lac)在大肠杆菌厌氧3-磷酸甘油脱氢酶基因(glpAB)呼吸调节研究中的应用。
J Bacteriol. 1984 Feb;157(2):591-8. doi: 10.1128/jb.157.2.591-598.1984.
4
Homology between CAP and Fnr, a regulator of anaerobic respiration in Escherichia coli.CAP与Fnr(大肠杆菌中无氧呼吸的一种调节因子)之间的同源性。
J Mol Biol. 1983 May 15;166(2):241-7. doi: 10.1016/s0022-2836(83)80011-4.
5
Proteins induced by anaerobiosis in Escherichia coli.大肠杆菌中厌氧诱导产生的蛋白质。
J Bacteriol. 1983 Apr;154(1):336-43. doi: 10.1128/jb.154.1.336-343.1983.
6
A new pair of M13 vectors for selecting either DNA strand of double-digest restriction fragments.一对用于选择双酶切限制片段任一条DNA链的新型M13载体。
Gene. 1982 Oct;19(3):269-76. doi: 10.1016/0378-1119(82)90016-6.
7
The pUC plasmids, an M13mp7-derived system for insertion mutagenesis and sequencing with synthetic universal primers.pUC质粒,一种源自M13mp7的用于插入诱变和使用合成通用引物进行测序的系统。
Gene. 1982 Oct;19(3):259-68. doi: 10.1016/0378-1119(82)90015-4.
8
Nucleotide sequence of the fnr gene and primary structure of the Enr protein of Escherichia coli.大肠杆菌fnr基因的核苷酸序列及Enr蛋白的一级结构。
Nucleic Acids Res. 1982 Oct 11;10(19):6119-30. doi: 10.1093/nar/10.19.6119.
9
Tn10 insertions in the pfkB region of Escherichia coli.大肠杆菌pfkB区域中的Tn10插入序列。
J Bacteriol. 1981 Sep;147(3):935-43. doi: 10.1128/jb.147.3.935-943.1981.
10
Cloning, restriction endonuclease mapping and post-transcriptional regulation of rpsA, the structural gene for ribosomal protein S1.核糖体蛋白S1的结构基因rpsA的克隆、限制性内切酶图谱分析及转录后调控
Mol Gen Genet. 1981;181(4):548-51. doi: 10.1007/BF00428751.