New shuttle vectors for Escherichia coli and Bacillus subtilis. III. Nucleotide sequence analysis of tetracycline resistance gene of pAM.ALPHA.1 and ori-177.

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  • 大腸菌と枯草菌で共用できるシャトルベクタ--3-pAMα1由来のテトラサイクリン耐性遺伝子とpACYC177由来の複製開始領域のDNAの塩基配列〔英文〕
  • ダイチョウキン ト コソウキン デ キョウヨウデキル シャトル ベクター 3
  • New shuttle vectors for Escherichia coli and Bacillus subtilis. II. Nucleotide sequence analysis of tetracycline resistance gene pAMα1 and ori-177
  • New shuttle vectors for Escherichia coli and Bacillus subtilis. III. Nucleotide sequence analysis of tetracycline resistance gene of pAMα1 and ori-177
  • III. Nucleotide sequence analysis of tetracycline resistance gene of pAMα1 and <i>ori</i>-177

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A small plasmid pHY163PLK (2519bp) was constructed from the shuttle vector pHY300PLK. pHY163PLK contains the replication origin of pACYC-177, the tetracycline resistance gene (tetα1) of pAMα1 derived from Streptococcus faecalis and eight continuous unique cloning sites of a polylinker region (EcoRI, SmaI, BamHI, SalI, PstI, BglII, XbaI and HindIII). pHY163PLK, a copy-number mutant, has one base substitution in RNA I region compared with that of p15A which is the ancestor of ori-pHY163PLK. The tetα1, which codes 458 amino acids (1374bp), is highly homologous to the TcR genes of other Gram-positive bacteria but completely different from the TcR gene encoded by pBR322 in Gram-negative bacteria. The regulatory region of tetα1 (constitutive type) has an insertion of seven base pairs in the leader peptide region of a related inducible TcR gene. (key words: tetracycline resistance gene; pAMα1; Streptococcus; nucleotide sequence; amino acid sequence)

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