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High-frequency electroporation and maintenance of pUC- and pBR-based cloning vectors in Pseudomonas stutzeri.
Pemberton, J M; Penfold, R J.
Afiliação
  • Pemberton JM; Microbiology Department, University of Queensland, St. Lucia, Brisbane, Australia.
Curr Microbiol ; 25(1): 25-9, 1992 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-1369188
ABSTRACT
A number of Escherichia coli cloning vectors, based on ColE1-like replicons, were shown to be maintained in Pseudomonas stutzeri ATCC 17588. A restrictionless mutant of P. stutzeri was isolated, and this strain was used to develop an efficient electroporation system. With the E. coli cloning vector pHSG298, transformation frequencies of up to 2 x 10(7) transformants/micrograms DNA were achieved. This frequency is comparable to that obtained for CaCl2-mediated transformation of E. coli; thus, direct cloning of DNA into P. stutzeri is feasible. As will be discussed, this may prove useful for cloning DNA from high mol% G + C genera in cases in which E. coli is not a suitable heterologous cloning host.
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Coleções: Bases de dados internacionais Base de dados: MEDLINE Assunto principal: Pseudomonas / Transformação Bacteriana / DNA Bacteriano / Técnicas Bacteriológicas / Clonagem Molecular / Plasmídeos de Bacteriocinas / Eletroquímica / Vetores Genéticos Idioma: Inglês Revista: Curr Microbiol Ano de publicação: 1992 Tipo de documento: Artigo País de afiliação: Austrália