• 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

萤火虫荧光素酶作为一种报告基因用于研究变形链球菌中的基因表达。

Firefly luciferase as a reporter to study gene expression in Streptococcus mutans.

作者信息

Goodman S D, Gao Q

机构信息

Department of Basic Sciences, University of Southern California School of Dentistry, 925 West 34th Street, Los Angeles, California 90089-0641, USA.

出版信息

Plasmid. 1999 Sep;42(2):154-7. doi: 10.1006/plas.1999.1416.

DOI:10.1006/plas.1999.1416
PMID:10489334
Abstract

The utility of firefly luciferase as a reporter was tested in Streptococcus mutans. Under control of an endogenous promoter, the luciferase coding sequence was strongly expressed, while a promoterless version was indistinguishable from the background. Luciferase activity was easily extracted and the assay rapid and reproducible. In addition, the half-life of luciferase activity was found to be comparable to those of other frequently used reporters. Thus, firefly luciferase can readily be used as a reporter in S. mutans, a useful alternative to methods requiring radioactive isotopes.

摘要

在变形链球菌中测试了萤火虫荧光素酶作为报告基因的效用。在内源启动子的控制下,荧光素酶编码序列强烈表达,而无启动子版本与背景无差异。荧光素酶活性易于提取,检测快速且可重复。此外,发现荧光素酶活性的半衰期与其他常用报告基因的半衰期相当。因此,萤火虫荧光素酶可轻易用作变形链球菌中的报告基因,是需要放射性同位素的方法的一种有用替代方法。

相似文献

1
Firefly luciferase as a reporter to study gene expression in Streptococcus mutans.萤火虫荧光素酶作为一种报告基因用于研究变形链球菌中的基因表达。
Plasmid. 1999 Sep;42(2):154-7. doi: 10.1006/plas.1999.1416.
2
Expression and in vivo determination of firefly luciferase as gene reporter in Saccharomyces cerevisiae.萤火虫荧光素酶作为基因报告基因在酿酒酵母中的表达及体内测定
Yeast. 1994 Oct;10(10):1321-7. doi: 10.1002/yea.320101009.
3
Expression and quantification of firefly luciferase under control of Rhizobium meliloti symbiotic promoters.在苜蓿根瘤菌共生启动子控制下萤火虫荧光素酶的表达与定量分析。
J Biolumin Chemilumin. 1991 Jul-Sep;6(3):177-84. doi: 10.1002/bio.1170060307.
4
A GUS/luciferase fusion reporter for plant gene trapping and for assay of promoter activity with luciferin-dependent control of the reporter protein stability.一种用于植物基因捕获以及通过荧光素依赖的报告蛋白稳定性控制来检测启动子活性的GUS/荧光素酶融合报告基因。
Plant Cell Physiol. 2007 Aug;48(8):1121-31. doi: 10.1093/pcp/pcm081. Epub 2007 Jun 27.
5
Optimized use of the firefly luciferase assay as a reporter gene in mammalian cell lines.萤火虫荧光素酶检测作为哺乳动物细胞系中报告基因的优化应用。
Biotechniques. 1989 Nov-Dec;7(10):1116-22.
6
Expression of firefly luciferase gene in Erwinia amylovora.萤火虫荧光素酶基因在梨火疫病菌中的表达。
Luminescence. 2003 Jul-Aug;18(4):207-13. doi: 10.1002/bio.726.
7
Use of a dual firefly and Renilla luciferase reporter gene assay to simultaneously determine drug selectivity at human corticotrophin releasing hormone 1 and 2 receptors.使用双荧光素酶和海肾荧光素酶报告基因检测法同时测定药物对人促肾上腺皮质激素释放激素1型和2型受体的选择性。
Anal Biochem. 2000 Jun 1;281(2):187-92. doi: 10.1006/abio.2000.4570.
8
Characterization of the gtfB and gtfC promoters from Streptococcus mutans GS-5.变形链球菌GS-5中gtfB和gtfC启动子的特性分析。
Plasmid. 2000 Jan;43(1):85-98. doi: 10.1006/plas.1999.1444.
9
Non-disruptive, real-time analyses of the metabolic status and viability of Streptococcus mutans cells in response to antimicrobial treatments.对变形链球菌细胞在抗菌治疗下的代谢状态和活力进行非侵入性实时分析。
J Microbiol Methods. 2005 May;61(2):161-70. doi: 10.1016/j.mimet.2004.11.012. Epub 2004 Dec 18.
10
One-step measurement of firefly luciferase activity in yeast.酵母中萤火虫荧光素酶活性的一步法测量
Yeast. 2003 Oct 15;20(13):1109-13. doi: 10.1002/yea.1024.

引用本文的文献

1
Illuminating the oral microbiome and its host interactions: tools and approaches for molecular microbiology studies.揭示口腔微生物组及其宿主相互作用:分子微生物学研究的工具和方法。
FEMS Microbiol Rev. 2023 Nov 1;47(6). doi: 10.1093/femsre/fuac050.
2
Cloning-independent plasmid construction for genetic studies in streptococci.用于链球菌遗传研究的非克隆依赖型质粒构建。
J Microbiol Methods. 2013 Aug;94(2):77-82. doi: 10.1016/j.mimet.2013.05.005. Epub 2013 May 12.
3
Cloning-independent and counterselectable markerless mutagenesis system in Streptococcus mutans.
链霉菌中独立于克隆且可反向选择的无标记基因突变系统。
Appl Environ Microbiol. 2011 Nov;77(22):8025-33. doi: 10.1128/AEM.06362-11. Epub 2011 Sep 23.
4
Role of GlnR in acid-mediated repression of genes encoding proteins involved in glutamine and glutamate metabolism in Streptococcus mutans.GlnR 在参与谷氨酸盐和谷氨酸代谢的蛋白编码基因的酸介导抑制中的作用在变异链球菌中。
Appl Environ Microbiol. 2010 Apr;76(8):2478-86. doi: 10.1128/AEM.02622-09. Epub 2010 Feb 19.
5
Genetic basis for conversion of rough-to-smooth colony morphology in Actinobacillus actinomycetemcomitans.伴放线放线杆菌粗糙型至光滑型菌落形态转变的遗传基础。
Infect Immun. 2005 Jun;73(6):3749-53. doi: 10.1128/IAI.73.6.3749-3753.2005.
6
The divergently transcribed Streptococcus parasanguis virulence-associated fimA operon encoding an Mn(2+)-responsive metal transporter and pepO encoding a zinc metallopeptidase are not coordinately regulated.编码锰(2+)响应性金属转运蛋白的远源转录副血链球菌毒力相关fimA操纵子和编码锌金属肽酶的pepO不受协同调控。
Infect Immun. 2002 Oct;70(10):5706-14. doi: 10.1128/IAI.70.10.5706-5714.2002.