携带uspA'::lux基因融合的大肠杆菌菌株和携带grpE'::lux融合的大肠杆菌菌株对毒物的反应相似。
Responses to toxicants of an Escherichia coli strain carrying a uspA'::lux genetic fusion and an E. coli strain carrying a grpE'::lux fusion are similar.
作者信息
Van Dyk T K, Smulski D R, Reed T R, Belkin S, Vollmer A C, LaRossa R A
机构信息
DuPont Company, Central Research and Development, Experimental Station, Wilmington, Delaware, USA.
出版信息
Appl Environ Microbiol. 1995 Nov;61(11):4124-7. doi: 10.1128/aem.61.11.4124-4127.1995.
Abstract
A transcriptional fusion of the Escherichia coli uspA promoter to luxCDABE was characterized and compared with a heat shock-responsive grpE'::lux fusion. Similarities in range and rank order of inducing conditions were observed; however, the magnitude of induction was typically greater for the grpE'::lux fusion strain.
摘要
对大肠杆菌uspA启动子与luxCDABE的转录融合体进行了表征，并与热休克反应性grpE'::lux融合体进行了比较。观察到诱导条件在范围和排序上的相似性；然而，对于grpE'::lux融合菌株，诱导程度通常更大。
相似文献
1
Responses to toxicants of an Escherichia coli strain carrying a uspA'::lux genetic fusion and an E. coli strain carrying a grpE'::lux fusion are similar.携带uspA'::lux基因融合的大肠杆菌菌株和携带grpE'::lux融合的大肠杆菌菌株对毒物的反应相似。
Appl Environ Microbiol. 1995 Nov;61(11):4124-7. doi: 10.1128/aem.61.11.4124-4127.1995.
2
Induced expression of the heat shock protein genes uspA and grpE during starvation at low temperatures and their influence on thermal resistance of Escherichia coli O157:H7.低温饥饿期间热休克蛋白基因uspA和grpE的诱导表达及其对大肠杆菌O157:H7耐热性的影响。
J Food Prot. 2003 Nov;66(11):2045-50. doi: 10.4315/0362-028x-66.11.2045.
3
Characterization of stress-responsive genes, hrcA-grpE-dnaK-dnaJ, from phytopathogenic Xanthomonas campestris.植物病原性野油菜黄单胞菌中应激反应基因hrcA-grpE-dnaK-dnaJ的特性分析
Arch Microbiol. 2001 Jul;176(1-2):121-8. doi: 10.1007/s002030100302.
4
Rapid and sensitive pollutant detection by induction of heat shock gene-bioluminescence gene fusions.通过诱导热休克基因-生物发光基因融合实现快速灵敏的污染物检测。
Appl Environ Microbiol. 1994 May;60(5):1414-20. doi: 10.1128/aem.60.5.1414-1420.1994.
5
Isolation and characterization of point mutations in the Escherichia coli grpE heat shock gene.大肠杆菌grpE热休克基因点突变的分离与鉴定
J Bacteriol. 1994 Nov;176(22):6965-73. doi: 10.1128/jb.176.22.6965-6973.1994.
6
Hypochlorous acid activates the heat shock and soxRS systems of Escherichia coli.次氯酸激活大肠杆菌的热休克系统和soxRS系统。
Appl Environ Microbiol. 1996 Nov;62(11):4003-8. doi: 10.1128/aem.62.11.4003-4008.1996.
7
The heat-shock-regulated grpE gene of Escherichia coli is required for bacterial growth at all temperatures but is dispensable in certain mutant backgrounds.大肠杆菌中受热激调节的grpE基因是细菌在所有温度下生长所必需的，但在某些突变背景下是可有可无的。
J Bacteriol. 1989 May;171(5):2748-55. doi: 10.1128/jb.171.5.2748-2755.1989.
8
A grpE mutant of Escherichia coli is more resistant to heat than the wild-type.
J Gen Microbiol. 1990 May;136(5):797-801. doi: 10.1099/00221287-136-5-797.
9
Immobilization of Escherichia coli expressing the lux genes of Xenorhabdus luminescens.固定表达发光杆菌属发光基因的大肠杆菌。
Appl Environ Microbiol. 1994 Oct;60(10):3862-3. doi: 10.1128/aem.60.10.3862-3863.1994.
10
Oxidative stress detection with Escherichia coli harboring a katG'::lux fusion.利用携带katG'::lux融合基因的大肠杆菌进行氧化应激检测。
Appl Environ Microbiol. 1996 Jul;62(7):2252-6. doi: 10.1128/aem.62.7.2252-2256.1996.
引用本文的文献
1
A three-colour stress biosensor reveals multimodal response in single cells and spatiotemporal dynamics of biofilms.三色压力生物传感器揭示了单细胞中的多模态响应和生物膜的时空动力学。
NPJ Biofilms Microbiomes. 2023 Aug 21;9(1):57. doi: 10.1038/s41522-023-00424-1.
2
Enhanced Bioactivity of Tailor-Made Glycolipid Enriched Manuka Honey.定制富含甘油酯的麦卢卡蜂蜜的生物活性增强。
Int J Mol Sci. 2022 Oct 10;23(19):12031. doi: 10.3390/ijms231912031.
3
Smartphone-Based Whole-Cell Biosensor Platform Utilizing an Immobilization Approach on a Filter Membrane Disk for the Monitoring of Water Toxicants.基于智能手机的全细胞生物传感器平台，利用在滤膜盘上的固定化方法，用于监测水毒剂。
Sensors (Basel). 2020 Sep 25;20(19):5486. doi: 10.3390/s20195486.
4
Metal complexation by histidine-rich peptides confers protective roles against cadmium stress in as revealed by proteomics analysis.蛋白质组学分析表明，富含组氨酸的肽与金属络合赋予了对镉胁迫的保护作用。
PeerJ. 2018 Jul 26;6:e5245. doi: 10.7717/peerj.5245. eCollection 2018.
5
Profiling the biological effects of wastewater samples via bioluminescent bacterial biosensors combined with estrogenic assays.通过生物发光细菌生物传感器结合雌激素测定法分析废水样本的生物学效应。
Environ Sci Pollut Res Int. 2017 Jan;24(1):33-41. doi: 10.1007/s11356-016-6050-5. Epub 2016 Feb 17.
6
Evaluative profiling of arsenic sensing and regulatory systems in the human microbiome project genomes.人类微生物组计划基因组中砷传感与调控系统的评估分析
Microbiol Insights. 2014 Nov 11;7:25-34. doi: 10.4137/MBI.S18076. eCollection 2014.
7
How novel methods can help discover more information about foodborne pathogens.新型方法如何有助于发现更多关于食源性病原体的信息。
Can J Infect Dis. 2000 May;11(3):142-53. doi: 10.1155/2000/364050.
8
Improved luciferase tagging system for Listeria monocytogenes allows real-time monitoring in vivo and in vitro.用于单核细胞增生李斯特菌的改良荧光素酶标记系统可实现体内和体外实时监测。
Appl Environ Microbiol. 2007 May;73(9):3091-4. doi: 10.1128/AEM.02940-06. Epub 2007 Mar 9.
9
Novel luciferase reporter system for in vitro and organ-specific monitoring of differential gene expression in Listeria monocytogenes.用于体外和器官特异性监测单核细胞增生李斯特菌中差异基因表达的新型荧光素酶报告系统。
Appl Environ Microbiol. 2006 Apr;72(4):2876-84. doi: 10.1128/AEM.72.4.2876-2884.2006.
10
Accelerated degradation of dipentyl phthalate by Fusarium oxysporum f. sp. pisi cutinase and toxicity evaluation of its degradation products using bioluminescent bacteria.尖孢镰刀菌豌豆专化型角质酶对邻苯二甲酸二戊酯的加速降解及其降解产物对发光细菌的毒性评价
Curr Microbiol. 2006 May;52(5):340-4. doi: 10.1007/s00284-005-0124-9. Epub 2006 Apr 1.
本文引用的文献
1
luxAB gene fusions with the arsenic and cadmium resistance operons of Staphylococcus aureus plasmid pI258.金黄色葡萄球菌质粒pI258的砷和镉抗性操纵子与luxAB基因的融合体
FEMS Microbiol Lett. 1993 Jun 15;110(2):231-8. doi: 10.1111/j.1574-6968.1993.tb06325.x.
2
Bioluminescent sensors for detection of bioavailable Hg(II) in the environment.用于检测环境中生物可利用汞（II）的生物发光传感器。
Appl Environ Microbiol. 1993 Sep;59(9):3083-90. doi: 10.1128/aem.59.9.3083-3090.1993.
3
Expression and role of the universal stress protein, UspA, of Escherichia coli during growth arrest.大肠杆菌通用应激蛋白UspA在生长停滞期间的表达及作用
Mol Microbiol. 1994 Feb;11(3):537-44. doi: 10.1111/j.1365-2958.1994.tb00334.x.
4
Rapid and sensitive pollutant detection by induction of heat shock gene-bioluminescence gene fusions.通过诱导热休克基因-生物发光基因融合实现快速灵敏的污染物检测。
Appl Environ Microbiol. 1994 May;60(5):1414-20. doi: 10.1128/aem.60.5.1414-1420.1994.
5
Regulation of the heat-shock response in bacteria.细菌中热休克反应的调控
Annu Rev Microbiol. 1993;47:321-50. doi: 10.1146/annurev.mi.47.100193.001541.
6
Sequence analysis and transcriptional regulation of the Escherichia coli grpE gene, encoding a heat shock protein.编码一种热休克蛋白的大肠杆菌grpE基因的序列分析及转录调控
Nucleic Acids Res. 1988 Aug 11;16(15):7545-62. doi: 10.1093/nar/16.15.7545.
7
Regulation of the vir genes of Agrobacterium tumefaciens plasmid pTiC58.根癌土壤杆菌质粒pTiC58的vir基因调控
J Bacteriol. 1987 Nov;169(11):5101-12. doi: 10.1128/jb.169.11.5101-5112.1987.
8
A microtiter plate-based system for the semiautomated growth and assay of bacterial cells for beta-galactosidase activity.一种基于微量滴定板的系统，用于细菌细胞的半自动化生长及β-半乳糖苷酶活性检测。
Anal Biochem. 1989 Aug 15;181(1):40-50. doi: 10.1016/0003-2697(89)90391-6.
9
Monitoring of naphthalene catabolism by bioluminescence with nah-lux transcriptional fusions.利用nah-lux转录融合通过生物发光监测萘的分解代谢。
J Bacteriol. 1990 Sep;172(9):4749-57. doi: 10.1128/jb.172.9.4749-4757.1990.
10
Cloning, mapping and nucleotide sequencing of a gene encoding a universal stress protein in Escherichia coli.大肠杆菌中一种编码通用应激蛋白的基因的克隆、定位与核苷酸测序
Mol Microbiol. 1992 Nov;6(21):3187-98. doi: 10.1111/j.1365-2958.1992.tb01774.x.
Zotero 插件