Literature DB >> 24393695

Direct facile screening of recombinant DNA vector constructs.

Paul T Winnard1, Rushi Challa1, Zaver M Bhujwalla2, Venu Raman3.   

Abstract

Direct efficient facile screening of bacterial transformants with the goal of selecting, retrieving, and using recombinant DNA is exemplified by simple visual-based colorimetric inspections or fluorescent protein-based assays. We describe pRedScript, which introduces the constitutive expression of a very bright red fluorescent protein into transformants. On agar plates, red colonies are simply visualized in ambient white light in stark contrast to recombinant transformants that are white. In addition, the bright red fluorescence of the reporter protein can also be harnessed as a sensitive signal for screening bacterial promoters during the development of optimized fermentation conditions.
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Recombinant DNA; Red color; Screening; mCherry

Mesh:

Substances:

Year:  2014        PMID: 24393695      PMCID: PMC4324639          DOI: 10.1016/j.ab.2013.12.034

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  16 in total

1.  Tuning genetic control through promoter engineering.

Authors:  Hal Alper; Curt Fischer; Elke Nevoigt; Gregory Stephanopoulos
Journal:  Proc Natl Acad Sci U S A       Date:  2005-08-25       Impact factor: 11.205

2.  Positive selection vector using the KillerRed gene.

Authors:  Xuedong Liu; Rui Shi; Dan Zou; Zaiyu Li; Xing Liu; Yanxia Chen; Xiaoguang Yang; Yanna Zhou; Dong Zheng
Journal:  Anal Biochem       Date:  2011-02-01       Impact factor: 3.365

3.  The sequence of spacers between the consensus sequences modulates the strength of prokaryotic promoters.

Authors:  P R Jensen; K Hammer
Journal:  Appl Environ Microbiol       Date:  1998-01       Impact factor: 4.792

4.  Filamentous coliphage M13 as a cloning vehicle: insertion of a HindII fragment of the lac regulatory region in M13 replicative form in vitro.

Authors:  J Messing; B Gronenborn; B Müller-Hill; P Hans Hopschneider
Journal:  Proc Natl Acad Sci U S A       Date:  1977-09       Impact factor: 11.205

5.  The pIC plasmid and phage vectors with versatile cloning sites for recombinant selection by insertional inactivation.

Authors:  J L Marsh; M Erfle; E J Wykes
Journal:  Gene       Date:  1984-12       Impact factor: 3.688

6.  The pUC plasmids, an M13mp7-derived system for insertion mutagenesis and sequencing with synthetic universal primers.

Authors:  J Vieira; J Messing
Journal:  Gene       Date:  1982-10       Impact factor: 3.688

7.  Construction and properties of a new cloning vehicle, allowing direct screening for recombinant plasmids.

Authors:  U Rüther
Journal:  Mol Gen Genet       Date:  1980

8.  A bacterial cloning vector using a mutated Aequorea green fluorescent protein as an indicator.

Authors:  S Inouye; H Ogawa; K Yasuda; K Umesono; F I Tsuji
Journal:  Gene       Date:  1997-04-21       Impact factor: 3.688

9.  Construction of a family of universal expression plasmid vectors.

Authors:  Z Hanna; C Fregeau; G Préfontaine; R Brousseau
Journal:  Gene       Date:  1984-10       Impact factor: 3.688

10.  Lambda ZAP: a bacteriophage lambda expression vector with in vivo excision properties.

Authors:  J M Short; J M Fernandez; J A Sorge; W D Huse
Journal:  Nucleic Acids Res       Date:  1988-08-11       Impact factor: 16.971

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