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July 1, 1984Journal of BacteriologyOpen Access

Regeneration of insertionally inactivated streptococcal DNA fragments after excision of transposon Tn916 in Escherichia coli: strategy for targeting and cloning of genes from gram-positive bacteria

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Authors

CGC Gawron-BurkeCairn UniversityDCDon B. ClewellUniversity of Michigan

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Gawron-Burke et al. (1984) studied this question.

synapsesocial.com/papers/6a6fbf50febe604dd7089995https://doi.org/10.1128/jb.159.1.214-221.1984
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Mapping of Streptococcus faecalis plasmids pAD1 and pAD2 and studies relating to transposition of Tn9171982 · 234 citations
  2. 2Fate of homospecific transforming DNA bound to Streptococcus sanguis1978 · 27 citations
  3. 3Chimeric streptococcal plasmids and their use as molecular cloning vehicles in Streptococcus sanguis (Challis)1980 · 94 citations
  4. 4Tetracycline resistance genes from Bacillus plasmid pAB124 confer decreased accumulation of the antibiotic in Bacillus subtilis but not in Escherichia coli1981 · 18 citations
  5. 5Evidence for Conjugal Transfer of a Streptococcus faecalis Transposon (Tn916) from a Chromosomal Site in the Absence of Plasmid DNA1981 · 73 citations