Literature DB >> 11682170

Green fluorescent protein--a bright idea for the study of bacterial protein localization.

G J Phillips1.   

Abstract

Use of the green fluorescent protein (GFP) of Aequorea victoria as a reporter for protein and DNA localization has provided sensitive, new approaches for studying the organization of the bacterial cell, leading to new insights into diverse cellular processes. GFP has many characteristics that make it useful for localization studies in bacteria, primarily its ability to fluoresce when fused to target polypeptides without the addition of exogenously added substrates. As an alternative to immunofluorescence microscopy, the expression of gfp gene fusions has been used to probe the function of cellular components fundamental for DNA replication, translation, protein export, and signal transduction, that heretofore have been difficult to study in living cells. Moreover, protein and DNA localization can now be monitored in real time, revealing that several proteins important for cell division, development and sporulation are dynamically localized throughout the cell cycle. The use of additional GFP variants that permit the labeling of multiple components within the same cell, and the use of GFP for genetic screens, should continue to make this a valuable tool for addressing complex questions about the bacterial cell.

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Year:  2001        PMID: 11682170     DOI: 10.1111/j.1574-6968.2001.tb10854.x

Source DB:  PubMed          Journal:  FEMS Microbiol Lett        ISSN: 0378-1097            Impact factor:   2.742


  16 in total

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Authors:  Tsuyoshi Kenri; Shintaro Seto; Atsuko Horino; Yuko Sasaki; Tsuguo Sasaki; Makoto Miyata
Journal:  J Bacteriol       Date:  2004-10       Impact factor: 3.490

Review 2.  Biofilms, a new approach to the microbiology of dental plaque.

Authors:  Jacob M ten Cate
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3.  Membrane topology mapping of the Na+-pumping NADH: quinone oxidoreductase from Vibrio cholerae by PhoA-green fluorescent protein fusion analysis.

Authors:  Ellen B Duffy; Blanca Barquera
Journal:  J Bacteriol       Date:  2006-10-13       Impact factor: 3.490

4.  Dynamic transcriptional response of Escherichia coli to inclusion body formation.

Authors:  Faraz Baig; Lawrence P Fernando; Mary Alice Salazar; Rhonda R Powell; Terri F Bruce; Sarah W Harcum
Journal:  Biotechnol Bioeng       Date:  2014-01-30       Impact factor: 4.530

5.  Vectors for ligation-independent construction of lacZ gene fusions and cloning of PCR products using a nicking endonuclease.

Authors:  Carrie J Oster; Gregory J Phillips
Journal:  Plasmid       Date:  2011-08-10       Impact factor: 3.466

6.  pMINERVA: A donor-acceptor system for the in vivo recombineering of scFv into IgG molecules.

Authors:  M Batonick; M M Kiss; E P Fuller; C M Magadan; E G Holland; Q Zhao; D Wang; B K Kay; M P Weiner
Journal:  J Immunol Methods       Date:  2016-02-03       Impact factor: 2.303

7.  Stable Expression of Modified Green Fluorescent Protein in Group B Streptococci To Enable Visualization in Experimental Systems.

Authors:  Matthew J Sullivan; Glen C Ulett
Journal:  Appl Environ Microbiol       Date:  2018-08-31       Impact factor: 4.792

8.  A Strategic Approach for Fluorescence Imaging of Membrane Proteins in a Native-like Environment.

Authors:  Jean-Marie Swiecicki; Jordan Tyler Santana; Barbara Imperiali
Journal:  Cell Chem Biol       Date:  2019-12-09       Impact factor: 8.116

Review 9.  Functioning nanomachines seen in real-time in living bacteria using single-molecule and super-resolution fluorescence imaging.

Authors:  Sheng-Wen Chiu; Mark C Leake
Journal:  Int J Mol Sci       Date:  2011-04-15       Impact factor: 5.923

10.  Producing a Mammalian GFP Expression Vector Containing Neomycin Resistance Gene.

Authors:  Manizheh Izadi; Maryam Abiri; Mohammad Keramatipour
Journal:  Avicenna J Med Biotechnol       Date:  2009-04
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