The Use of the Bacillus Species to Express the Bacillus Anthracis Toxin Genes for Vaccine Studies.

Abstract

We have constructed vectors for the high-level expression of the anthrax toxin genes. We have cloned the T7 RNA polymerase gene downstream from the IPTG-inducible promoter from pSI-1. IPTG induces expression of the T7 RNA polymerase when the 1acI repressor is inactivated. This integration plasmid has been inserted into the genome of Bacillus anthracis. Shuttle vectors for the expression of the individual anthrax toxin genes (derived from pDRl8l) consists of the replication components from pUBi110, a kanamycin resistance gene and the multi cloning sequence from pET21a, which contains the T7 RNA polymerase promoter and terminator. The individual toxin genes have been inerted into this plasmid. Six recombinant IZAP clones which contain B. anthracis DNA sequences homologous to the spoOH gene of B. subtilts have been isolated. The spo0H gene in the Bacillus species is required for sporulation This gene will be used to produce an asporogenic B. anthracis.

Open PDF

Document Details

Document Type
Technical Report
Publication Date
Jun 30, 1995
Accession Number
ADA297154

Entities

People

  • Donald L. Robinson
  • Earl Woolley

Organizations

  • Brigham Young University

Tags

DTIC Thesaurus Topics

  • Anti-Bacterial Agents
  • Bacteria
  • Biochemistry
  • Chemical Reactions
  • Chemical Synthesis
  • Chemistry
  • Gene Expression
  • Genetic Code
  • Genetics
  • Microbiology
  • Polymerase Chain Reaction
  • Recombinant Dna
  • Resistance
  • Sequence Analysis
  • Sequences
  • Spores
  • Transcription Factors

Fields of Study

  • Biology

Readers

  • Microbial Pathology
  • Molecular Genetics

Technology Areas

  • Biotechnology