
3D-Cry toxins, produced by the entomopathogenic bacterium Bacillus thuringiensis, have been extensively mutated in order to elucidate their elegant and complex mechanism of action necessary to kill susceptible insects. Together with the study of the resistant insects, 3D-Cry toxin mutants represent one of the pillars to understanding how these toxins exert their activity on their host. The principle is simple, if an amino acid is involved and essential in the mechanism of action, when substituted, the activity of the toxin will be diminished. However, some of the constructed 3D-Cry toxin mutants have shown an enhanced activity against their target insects compared to the parental toxins, suggesting that it is possible to produce novel versions of the natural toxins with an improved performance in the laboratory. In this report, all mutants with an enhanced activity obtained by accident in mutagenesis studies, together with all the variants obtained by rational design or by directed mutagenesis, were compiled. A description of the improved mutants was made considering their historical context and the parallel development of the protein engineering techniques that have been used to obtain them. This report demonstrates that artificial 3D-Cry toxins made in laboratories are a real alternative to natural toxins.
in vitro evolution, Toxin enhancement, Bacillus thuringiensis Toxins, toxin enhancement, Protein Conformation, rational design, R, Bacillus thuringiensis, Review, In vitro evolution, 3D-Cry toxins, Endotoxins, Hemolysin Proteins, Structure-Activity Relationship, Rational design, <i>Bacillus thuringiensis</i>, Mutation, Mutagenesis, Site-Directed, Medicine
in vitro evolution, Toxin enhancement, Bacillus thuringiensis Toxins, toxin enhancement, Protein Conformation, rational design, R, Bacillus thuringiensis, Review, In vitro evolution, 3D-Cry toxins, Endotoxins, Hemolysin Proteins, Structure-Activity Relationship, Rational design, <i>Bacillus thuringiensis</i>, Mutation, Mutagenesis, Site-Directed, Medicine
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