Literature DB >> 2656460

A synthetic translation-terminator gene. A tool for dissecting the translation direction of a gene.

I N Maruyama1, K Horikoshi, Y Nagase, M Soma, M Nobuhara, S Yasuda, Y Hirota.   

Abstract

A 41-nucleotide-long duplex DNA, which contains the translation termination codon TAA in six reading frames and lactose operator sequence of Escherichia coli, has been synthesized. This fragment may be useful not only for producing a truncated protein encoded in a plasmid, but also for the identification of the precise coding region and translation direction of a bacterial gene in the cloned chromosomal segment. The synthetic fragment was inserted into beta-lactamase structural gene in pBR322 in order to test the in vivo activity. The plasmid produced mutant beta-lactamase reduced in size, as expected from the insertion site, and rendered the host bacterium constitutive for beta-galactosidase. Thus, termination codons and lactose operator in synthetic nucleotide appear to be functional in vivo.

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Year:  1989        PMID: 2656460     DOI: 10.1016/0735-0651(89)90011-3

Source DB:  PubMed          Journal:  Gene Anal Tech        ISSN: 0735-0651


  3 in total

1.  Genetic analyses of processing involving C-terminal cleavage in penicillin-binding protein 3 of Escherichia coli.

Authors:  H Hara; Y Nishimura; J Kato; H Suzuki; H Nagasawa; A Suzuki; Y Hirota
Journal:  J Bacteriol       Date:  1989-11       Impact factor: 3.490

2.  Cloning, mapping, and characterization of the Escherichia coli prc gene, which is involved in C-terminal processing of penicillin-binding protein 3.

Authors:  H Hara; Y Yamamoto; A Higashitani; H Suzuki; Y Nishimura
Journal:  J Bacteriol       Date:  1991-08       Impact factor: 3.490

3.  Escherichia coli parA is an allele of the gyrB gene.

Authors:  J Kato; Y Nishimura; H Suzuki
Journal:  Mol Gen Genet       Date:  1989-05
  3 in total

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