Literature DB >> 3322286

A method to isolate DNA sequences that are promoter-active in Escherichia coli and in yeast.

J W Kwak1, J Kim, O J Yoo, M H Han.   

Abstract

A method convenient for isolation of DNA sequences capable of directing gene transcription in both organisms of E. coli and yeast is described. The method is composed of sequential steps of phenotypic selection for chloramphenicol resistance, first in E. coli and then in yeast. A series of promoter-probe, shuttle plasmid vectors between yeast and E. coli were constructed and utilized in the method.

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Year:  1987        PMID: 3322286     DOI: 10.1016/0006-291x(87)90485-2

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  2 in total

1.  The Mu1 transposable element of maize contains two promoter signals recognized by the Escherichia coli RNA polymerase.

Authors:  L Del Giudice; F Manna; D R Massardo; M Motto; P Alifano; K Wolf
Journal:  Mol Gen Genet       Date:  1990-06

2.  Expression enhancement of the Tn5 neomycin-resistance gene by removal of upstream ATG sequences and its use for probing heterologous upstream activating sequences in yeast.

Authors:  S Yagi; K Yagi-Tanaka; J Yoshioka; M Suzuki
Journal:  Curr Genet       Date:  1993 Jul-Aug       Impact factor: 3.886

  2 in total

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