In vivo recombination and the production of hybrid genes

Sabina Calogero, Marco E. Bianchi, Alessandro Galizzi

Research output: Contribution to journalArticle

Abstract

In vivo recombination between homologous genes is increasingly being favoured as a means of generating proteins with altered and novel specificities. The typical procedure requires the cloning of two related genes on a single replicative plasmid of Escherichia coli and the selection or screening of recombinants. Up to now the recombination process between the cloned genes was generally thought to involve the recA function and the availability of free ends in the DNA molecule to be recombined. Our results show that neither is necessary. Recombinants are obtained by simply growing the bacteria that host the plasmid carrying the two cloned genes.

Original languageEnglish
Pages (from-to)41-44
Number of pages4
JournalFEMS Microbiology Letters
Volume97
Issue number1-2
DOIs
Publication statusPublished - Oct 1 1992

Fingerprint

Genetic Recombination
Genes
Plasmids
Organism Cloning
Escherichia coli
Bacteria
DNA
Proteins

Keywords

  • Protein engineering
  • recA
  • Recombination

ASJC Scopus subject areas

  • Genetics
  • Molecular Biology
  • Applied Microbiology and Biotechnology
  • Microbiology

Cite this

In vivo recombination and the production of hybrid genes. / Calogero, Sabina; Bianchi, Marco E.; Galizzi, Alessandro.

In: FEMS Microbiology Letters, Vol. 97, No. 1-2, 01.10.1992, p. 41-44.

Research output: Contribution to journalArticle

Calogero, Sabina ; Bianchi, Marco E. ; Galizzi, Alessandro. / In vivo recombination and the production of hybrid genes. In: FEMS Microbiology Letters. 1992 ; Vol. 97, No. 1-2. pp. 41-44.
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