Construction and characterization of a novel maltose inducible expression vector in Bacillus subtilis

Biotechnol Lett. 2006 Nov;28(21):1713-8. doi: 10.1007/s10529-006-9146-z. Epub 2006 Aug 3.

Abstract

A maltose-inducible expression vector in Bacillus subtilis has been developed and characterized. The vector permitted beta-galactosidase expression at a high level (maximum activity, 8.16 U/ml) when induced and its expression was markedly repressed by glucose. Using this vector, we successfully expressed the other two genes, bioA and vgb. This thus provided a potential expression system for cloned genes in B. subtilis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacillus subtilis / genetics*
  • Bacillus subtilis / metabolism
  • Bacterial Proteins / metabolism
  • Enzyme Induction
  • Gene Expression Regulation, Bacterial / genetics*
  • Genetic Vectors / biosynthesis
  • Genetic Vectors / genetics*
  • Hemeproteins / metabolism
  • Maltose / metabolism
  • Operon / genetics*
  • Promoter Regions, Genetic
  • Transaminases / metabolism
  • Transformation, Bacterial
  • beta-Galactosidase / metabolism

Substances

  • Bacterial Proteins
  • Hemeproteins
  • Vgb protein, Bacteria
  • Maltose
  • Transaminases
  • BioA protein, bacteria
  • beta-Galactosidase