A novel Bacillus subtilis expression vector based on bacteriophage φ105

This publication has 20 references indexed in Scilit:

• Site-directed mutagenesis of β-lactamase I. Single and double mutants of Glu-166 and Lys-73
  Biochemical Journal, 1990
• Structurally stable Bacillus subtilis cloning vectors
  Gene, 1990
• A new bacteriophage vector for cloning in Bacillus subtilis and the use of ø105 for protein synthesis in maxicells
  Gene, 1989
• Differential gene expression during sporulation in Bacillus subtilis: regulation of the spoVJ gene
  Molecular Microbiology, 1989
• Upper limit for DNA packaging by Bacillus subtilis bacteriophage ϕ 105: Isolation of phage deletion mutants by induction of oversized prophages
  Molecular Genetics and Genomics, 1987
• Mutations of the Escherichia coli lacUV5 promoter resulting in increased expression in Bacillus subtilis
  Molecular Genetics and Genomics, 1987
• Nucleotide sequence and mutational analysis of an immunity repressor gene fromBacillus subtilistemperate phage ø105
  Nucleic Acids Research, 1985
• “Western Blotting”: Electrophoretic transfer of proteins from sodium dodecyl sulfate-polyacrylamide gels to unmodified nitrocellulose and radiographic detection with antibody and radioiodinated protein A
  Analytical Biochemistry, 1981
• A method for construction of specialized transducing phage ϱ11 of Bacillus subtilis
  Gene, 1979
• 6 β-Bromopenicillanic acid inactivates β-lactamase I
  Biochemical Journal, 1979