Literature DB >> 23592493

White and green screening with circular polymerase extension cloning for easy and reliable cloning.

Elizabeth B Speltz1, Lynne Regan.   

Abstract

Cloning is an essential prerequisite to test protein design and engineering ideas. However, it is often time consuming, unreliable, and therefore frustrating. Here, we present a streamlined cloning strategy that incorporates a powerful white and green screening protocol to identify colonies with inserts. We use circular polymerase extension cloning, which is both ligation and sequence independent. Furthermore, our entire procedure requires only three quick steps and one enzyme making it easy to use, inexpensive, and tractable. We anticipate that this method will be particularly useful for protein engineers who frequently subclone or make focused deletion, insertion, or substitution libraries.
© 2013 The Protein Society.

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Year:  2013        PMID: 23592493      PMCID: PMC3690724          DOI: 10.1002/pro.2268

Source DB:  PubMed          Journal:  Protein Sci        ISSN: 0961-8368            Impact factor:   6.725


  13 in total

1.  pGreen-S: a clone vector bearing absence of enhanced green fluorescent protein for screening recombinants.

Authors:  Jinbao Tang; Shujuan Liang; Jinbao Zhang; Zhiqin Gao; Suhua Zhang
Journal:  Anal Biochem       Date:  2009-02-10       Impact factor: 3.365

2.  Accurate insertional inactivation of lacZalpha: construction of pTrueBlue and M13TrueBlue cloning vectors.

Authors:  S N Slilaty; S Lebel
Journal:  Gene       Date:  1998-06-15       Impact factor: 3.688

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Journal:  Methods Enzymol       Date:  1987       Impact factor: 1.600

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

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Authors:  C Yanisch-Perron; J Vieira; J Messing
Journal:  Gene       Date:  1985       Impact factor: 3.688

6.  Overlap extension PCR cloning: a simple and reliable way to create recombinant plasmids.

Authors:  Anton V Bryksin; Ichiro Matsumura
Journal:  Biotechniques       Date:  2010-06       Impact factor: 1.993

7.  Independent and tight regulation of transcriptional units in Escherichia coli via the LacR/O, the TetR/O and AraC/I1-I2 regulatory elements.

Authors:  R Lutz; H Bujard
Journal:  Nucleic Acids Res       Date:  1997-03-15       Impact factor: 16.971

8.  A novel prokaryotic vector for identification and selection of recombinants: direct use of the vector for expression studies in E. coli.

Authors:  Sampali Banerjee; Jitendra Kumar; Anjali Apte-Deshpande; Sriram Padmanabhan
Journal:  Microb Cell Fact       Date:  2010-05-11       Impact factor: 5.328

9.  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

10.  OligoCalc: an online oligonucleotide properties calculator.

Authors:  Warren A Kibbe
Journal:  Nucleic Acids Res       Date:  2007-04-22       Impact factor: 16.971

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  3 in total

Review 1.  A designed repeat protein as an affinity capture reagent.

Authors:  Elizabeth B Speltz; Rebecca S H Brown; Holly S Hajare; Christian Schlieker; Lynne Regan
Journal:  Biochem Soc Trans       Date:  2015-10       Impact factor: 5.407

2.  A new method for post-translationally labeling proteins in live cells for fluorescence imaging and tracking.

Authors:  M Hinrichsen; M Lenz; J M Edwards; O K Miller; S G J Mochrie; P S Swain; U Schwarz-Linek; L Regan
Journal:  Protein Eng Des Sel       Date:  2017-12-01       Impact factor: 1.650

3.  Replacing Standard Reporters from Molecular Cloning Plasmids with Chromoproteins for Positive Clone Selection.

Authors:  Margarita Daniela Tafoya-Ramírez; Felipe Padilla-Vaca; Ana Patricia Ramírez-Saldaña; Josué Daniel Mora-Garduño; Ángeles Rangel-Serrano; Naurú Idalia Vargas-Maya; Luz Janeth Herrera-Gutiérrez; Bernardo Franco
Journal:  Molecules       Date:  2018-05-31       Impact factor: 4.411

  3 in total

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