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pubmed-article:11078653pubmed:abstractTextA useful method for inserting any DNA fragment into the chromosome of Neisseriae has been developed. The method relies on recombination-proficient vector plasmid pNLE1, a pUC19 derivative containing (1) genes conferring resistance to ampicillin and erythromycin, as selectable markers; (2) a chromosomal region necessary for its integration into the Neisseria chromosome; (3) a specific uptake sequence which is required for natural transformation; (4) a promoter capable of functioning in Neisseria; and (5) several unique restriction sites useful for cloning. pNLE1 integrates into the leuS region of the neisserial chromosome at high frequencies by transformation-mediated recombination. The usefulness of this vector has been demonstrated by cloning the tetracycline-resistance gene (tet) and subsequently inserting the tet gene into the meningococcal chromosome.lld:pubmed
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pubmed-article:11078653pubmed:copyrightInfoCopyright 2000 Academic Press.lld:pubmed
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pubmed-article:11078653pubmed:volume44lld:pubmed
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pubmed-article:11078653pubmed:pagination275-9lld:pubmed
pubmed-article:11078653pubmed:dateRevised2008-11-21lld:pubmed
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pubmed-article:11078653pubmed:articleTitleA new vector for insertion of any DNA fragment into the chromosome of transformable Neisseriae.lld:pubmed
pubmed-article:11078653pubmed:affiliationDipartimento di Biologia e Patologia Cellulare e Molecolare "L. Califano,", Università di Napoli "Federico II,", Centro di Endocrinologia ed Oncologia Sperimentale "G. Salvatore" of the Consiglio Nazionale delle Ricerche, Naples, Italy.lld:pubmed
pubmed-article:11078653pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:11078653pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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