Open AccessExpression of the insecticidal crystal protein gene from a Gram‐positive Bacillus thuringiensis in a Gram‐negative Pseudomonas fluorescens mediated by protoplast fusion
Author(s) -
Rajendra Narayanan,
Sivamani E.,
Jayaraman Kunthala
Publication year - 1994
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 - 10.1111/j.1574-6968.1994.tb07151.x
Subject(s) - bacillus thuringiensis , pseudomonas fluorescens , biology , microbiology and biotechnology , protoplast , toxin , molecular mass , bacillales , bacteria , biochemistry , genetics , bacillus subtilis , enzyme
Protoplast fusion between a Gram‐negative strain Pseudomonas fluorescens having plant growth promoting activities and a Gram‐positive Bacillus thuringiensis var. kurstaki HD 73 possessing insecticidal activity, was carried out to generate P. fluorescens hybrids possessing insecticidal activity. The antibiotic resistance markers of P. fluorescens (rif r , nal r ) and the immunoreactivity to the antiserum raised against the crystal proteins of B. thuringiensis var. galleriae were used as selection markers for the hybrids. The hybrids exhibited lethal but differential activity in Heliothis armigera and in Spodoptera litura when compared to the parenthal B. thuringiensis strain. The anti‐feedant activity which is characteristic of B. thuringiensis toxin was not observed in the hybrids. Although the presence of sequences homologous to the cloned insecticidal gene of B. thuringiensis was demonstrated, the Western blot analysis of cell extract of the hybrid (PK 105) showed that only low molecular mass crystal proteins (less than 40 kDa) could be detected under denaturing conditions. It indicates that the high molecular mass toxin peptide may be degraded by proteolysis. Besides this, a clear separation of lethal and anti‐feedant activity of the B. thuringiensis toxin has been observed by this study.