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Journal of Bacteriology, October 1999, p. 6103-6107, Vol. 181, No. 19
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Analysis of Mutations in the Pore-Forming Region
Essential for Insecticidal Activity of a Bacillus
thuringiensis
-Endotoxin
A. S.
Manoj Kumar and
A. I.
Aronson*
Department of Biological Sciences, Purdue
University, West Lafayette, Indiana 47907
Received 8 March 1999/Accepted 29 July 1999
The Bacillus thuringiensis insecticidal
-endotoxins
have a three-domain structure, with the seven amphipathic helices which comprise domain I being essential for toxicity. To better define the
function of these helices in membrane insertion and toxicity, either
site-directed or random mutagenesis of two regions was performed.
Thirty-nucleotide segments in the B. thuringiensis cry1Ac1
gene, encoding parts of helix
4 and the loop connecting helices
4
and
5, were randomly mutagenized. This hydrophobic region of the
toxin probably inserts into the membrane as a hairpin. Site-directed
mutations were also created in specific surface residues of helix
3
in order to increase its hydrophobicity. Among 12 random mutations in
helix
4, 5 resulted in the total loss of toxicity for Manduca
sexta and Heliothis virescens, another caused a
significant increase in toxicity, and one resulted in decreased
toxicity. None of the nontoxic mutants was altered in toxin stability,
binding of toxin to a membrane protein, or the ability of the toxin to
aggregate in the membrane. Mutations in the loop connecting helices
4 and
5 did not affect toxicity, nor did mutations in
3, which
should have enhanced the hydrophobic properties of this helix. In
contrast to mutations in helix
5, those in helix
4 which
inactivated the toxin did not affect its capacity to oligomerize in the
membrane. Despite the formation of oligomers, there was no ion flow as
measured by light scattering. Helix
5 is important for
oligomerization and perhaps has other functions, whereas helix
4
must have a more direct role in establishing the properties of the channel.
*
Corresponding author. Mailing address: Department of
Biological Sciences, Purdue University, W. Lafayette, IN 47906. Phone: (765) 494 4992. Fax: (765) 494 0876. E-mail:
aaronson{at}bilbo.bio.purdue.edu.
Journal of Bacteriology, October 1999, p. 6103-6107, Vol. 181, No. 19
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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