Literature DB >> 2107530

Heat-inducible translational coupling in Bacillus subtilis.

S Fujiwara1, N Tsubokura, Y Kurusu, K Minami, Y Kobayashi.   

Abstract

Bacillus subtilis plasmid pGR71 is a promoter-probe shuttle vector derived from pUB110. The expression of the cat gene on pGR71 in B. subtilis requires the insertion of a Bacillus promoter and a ribosomal binding site (RBS) into the HindIII cloning site immediately upstream from the cat gene. A recombinant plasmid of pGR71, named pGR71-369, was obtained by a spontaneous deletion of a fragment containing most of the inserted HindIII fragment and the replication origin necessary for multiplication in Escherichia coli. The expression of the cat gene in B. subtilis cells carrying this plasmid was inducible by heat. Nucleotide sequence analysis of the upstream region of the cat gene, deletion analysis, and dot blot hybridization analysis of mRNA in various conditions revealed that the cat gene was expressed by heat-inducible translational coupling and that the regulatory region of heat inducibility was present in the upstream region of the cat gene.

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Year:  1990        PMID: 2107530      PMCID: PMC330321          DOI: 10.1093/nar/18.4.739

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  45 in total

1.  STRAND SEPARATION AND SPECIFIC RECOMBINATION IN DEOXYRIBONUCLEIC ACIDS: BIOLOGICAL STUDIES.

Authors:  J Marmur; D Lane
Journal:  Proc Natl Acad Sci U S A       Date:  1960-04       Impact factor: 11.205

2.  mRNA secondary structure in an open reading frame reduces translation efficiency in Bacillus subtilis.

Authors:  M Kubo; T Imanaka
Journal:  J Bacteriol       Date:  1989-07       Impact factor: 3.490

3.  Nucleotide sequence analysis of the chloramphenicol resistance transposon Tn9.

Authors:  N K Alton; D Vapnek
Journal:  Nature       Date:  1979 Dec 20-27       Impact factor: 49.962

4.  Mutational alterations of translational coupling in the L11 ribosomal protein operon of Escherichia coli.

Authors:  F Sor; M Bolotin-Fukuhara; M Nomura
Journal:  J Bacteriol       Date:  1987-08       Impact factor: 3.490

5.  Translational coupling at an intercistronic boundary of the Escherichia coli galactose operon.

Authors:  D Schümperli; K McKenney; D A Sobieski; M Rosenberg
Journal:  Cell       Date:  1982-10       Impact factor: 41.582

Review 6.  Attenuation in the control of expression of bacterial operons.

Authors:  C Yanofsky
Journal:  Nature       Date:  1981-02-26       Impact factor: 49.962

7.  Recovery of DNA from gels.

Authors:  H O Smith
Journal:  Methods Enzymol       Date:  1980       Impact factor: 1.600

8.  Cloning and characterization of a 12-gene cluster from Bacillus subtilis encoding nine enzymes for de novo purine nucleotide synthesis.

Authors:  D J Ebbole; H Zalkin
Journal:  J Biol Chem       Date:  1987-06-15       Impact factor: 5.157

9.  Structure of the Bacillus subtilis pyrimidine biosynthetic (pyr) gene cluster.

Authors:  C G Lerner; B T Stephenson; R L Switzer
Journal:  J Bacteriol       Date:  1987-05       Impact factor: 3.490

10.  Translational coupling in Bacillus subtilis of a heterologous Bacillus subtilis-Escherichia coli gene fusion.

Authors:  T I Zaghloul; F Kawamura; R H Doi
Journal:  J Bacteriol       Date:  1985-11       Impact factor: 3.490

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  2 in total

1.  Transcription of Clostridium cellulovorans cellulosomal cellulase and hemicellulase genes.

Authors:  Sung Ok Han; Hideaki Yukawa; Masayuki Inui; Roy H Doi
Journal:  J Bacteriol       Date:  2003-04       Impact factor: 3.490

2.  Quantitation of the capacity of the secretion apparatus and requirement for PrsA in growth and secretion of alpha-amylase in Bacillus subtilis.

Authors:  M Vitikainen; T Pummi; U Airaksinen; E Wahlström; H Wu; M Sarvas; V P Kontinen
Journal:  J Bacteriol       Date:  2001-03       Impact factor: 3.490

  2 in total

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