Literature DB >> 6323250

Overproduction of Escherichia coli NusA protein.

P O Olins, B D Erickson, R R Burgess.   

Abstract

The nusA gene of Escherichia coli has been cloned into the plasmid vector pKC30 under the control of the inducible lambda pL promoter. When a strain carrying this plasmid is induced, NusA protein is overproduced more than 100-fold and constitutes 20-30% of the total cellular protein. The NusA protein purified from this strain appears identical to authentic NusA protein in its migration on SDS polyacrylamide gels and on isoelectric focusing gels. It is also able to function properly in in vitro termination and antitermination assays and in its ability to bind to E. coli core RNA polymerase.

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Year:  1983        PMID: 6323250     DOI: 10.1016/0378-1119(83)90031-8

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  2 in total

1.  Efficient modification of E. coli RNA polymerase in vitro by the N gene transcription antitermination protein of bacteriophage lambda.

Authors:  Y Goda; J Greenblatt
Journal:  Nucleic Acids Res       Date:  1985-04-11       Impact factor: 16.971

2.  The Escherichia coli rep mutation. X. Consequences of increased and decreased Rep protein levels.

Authors:  J Colasanti; D T Denhardt
Journal:  Mol Gen Genet       Date:  1987-09
  2 in total

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