Literature DB >> 12405557

Positive selection vectors.

Young-Jun Choi1, Tsung-Tsan Wang, Byong H Lee.   

Abstract

This review describes information concerning positive selection vectors on their mechanism, classification, property, and limitation. A total of 72 positive selection vectors collected were discussed. Positive selection vectors can reduce background and directly screen transformants containing cloned DNA fragments. The mechanisms to perform positive selection include insertional inactivation and the replacement of functional genes of the vectors. In general, the former is much more convenient than the latter. The functional genes are controlled either by their promoters or by heterologous promoters introduced. On the basis of the structures, positive selection vectors could be classified into five groups. The positive selection vectors are commonly based on the mechanisms of lethal genes and the sensitivity of compounds. The vectors, with molecular weights ranging from 2.6 to 17.0 kb, have diverse genetic markers and wide host ranges, including Escherichia coli, Bacillus, Streptomyces, lactic acid bacteria, yeasts, and mammalian cells. Although some limitations exist for using some positive selection vectors, they are useful in recombinant DNA experiments.

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Year:  2002        PMID: 12405557     DOI: 10.1080/07388550290789504

Source DB:  PubMed          Journal:  Crit Rev Biotechnol        ISSN: 0738-8551            Impact factor:   8.429


  6 in total

1.  A strategy for in-house production of a positive selection cloning vector from the commercial pJET1.2/blunt cloning vector at minimal cost.

Authors:  Omar Nawawi; Mohd Puad Abdullah; Chong Yu Lok Yusuf
Journal:  3 Biotech       Date:  2022-08-09       Impact factor: 2.893

2.  Automated seamless DNA co-transformation cloning with direct expression vectors applying positive or negative insert selection.

Authors:  Natacha Olieric; Melanie Kuchen; Sandro Wagen; Marion Sauter; Stephanie Crone; Sonia Edmondson; Daniel Frey; Christian Ostermeier; Michel O Steinmetz; Rolf Jaussi
Journal:  BMC Biotechnol       Date:  2010-08-09       Impact factor: 2.563

3.  Characterization and heterologous gene expression of a novel esterase from Lactobacillus casei CL96.

Authors:  Young J Choi; Carlos B Miguez; Byong H Lee
Journal:  Appl Environ Microbiol       Date:  2004-06       Impact factor: 4.792

4.  pELMO, an optimised in-house cloning vector.

Authors:  Andrea E Ramos; Marina Muñoz; Darwin A Moreno-Pérez; Manuel A Patarroyo
Journal:  AMB Express       Date:  2017-01-24       Impact factor: 3.298

5.  IRDL cloning: a one-tube, zero-background, easy-to-use, directional cloning method improves throughput in recombinant DNA preparation.

Authors:  Jiancai Wang; Ronghua Xu; Aizhong Liu
Journal:  PLoS One       Date:  2014-09-22       Impact factor: 3.240

6.  A positive Selection Escherichia Coli Recombinant Protein Expression Vector for One-Step Cloning.

Authors:  Shinto James; Vikas Jain
Journal:  Front Bioeng Biotechnol       Date:  2022-01-03
  6 in total

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