Open AccessStable integration and expression of mosquito‐larvicidal genes from Bacillus thuringiensis subsp. israelensis and Bacillus sphaericus into the chromosome of Enterobacter amnigenus : a potential breakthrough in mosquito biocontrol
Author(s) -
Tanapongpipat Sutipa,
Nantapong Nawarat,
Cole Jeffrey,
Panyim Sakol
Publication year - 2003
Publication title -
fems microbiology letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.899
H-Index - 151
eISSN - 1574-6968
pISSN - 0378-1097
DOI - 10.1016/s0378-1097(03)00203-9
Subject(s) - biology , bacillus sphaericus , bacillus thuringiensis , gene , microbiology and biotechnology , genetics , pore forming toxin , homologous recombination , plasmid , bacillus subtilis , toxin , bacillales , bacteria , microbial toxins
Previously, we have successfully integrated a spectinomycin/streptomycin resistance gene into Enterobacter amnigenus strain An11, a potential host for mosquito control, using in vivo recombination via homologous recombination (An11S4::Ω). We now report the successful transfer of two mosquito‐larvicidal genes, cry4B from Bacillus thuringiensis subsp. israelensis and binary toxin genes from Bacillus sphaericus , into the host genome. To facilitate the screening procedure, the E. amnigenus derivative, An11S4::Ω, was used as a host. The integration of both toxin genes by two successive crossover events interrupted the Ω region yielding two integrants designated An11S4:: cry4B and An11S4::Ω:: bin , respectively. Differences in the integration efficiency of these toxin genes were observed. The presence of both genes in the target sites of the host genome was verified by PCR. Cry4B was expressed weakly from An11S4:: cry4B , but no expression of the binary toxin gene could be detected from An11S4::Ω:: bin . Nevertheless, these two integrants exhibited mosquito‐larvicidal activity against Aedes and Culex , suggesting that both proteins were expressed, but at very low levels.