Role of Alkaline Phosphatase from Manduca sexta in the Mechanism of Action of Bacillus thuringiensis Cry1Ab Toxin

被引:137
作者
Arenas, Ivan [1 ]
Bravo, Alejandra [1 ]
Soberon, Mario [1 ]
Gomez, Isabel [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Inst Biotecnol, Dept Mol Microbiol, Cuernavaca 62250, Morelos, Mexico
基金
美国农业部; 美国国家卫生研究院;
关键词
BRUSH-BORDER MEMBRANE; AMINOPEPTIDASE-N-RECEPTOR; OLIGOMERIC PRE-PORE; DELTA-ENDOTOXIN; DOMAIN-II; HELIOTHIS-VIRESCENS; BINDING-PROTEINS; LYMANTRIA-DISPAR; LARVAL MIDGUT; CYT TOXINS;
D O I
10.1074/jbc.M109.085266
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cry toxins produced by Bacillus thuringiensis have been recognized as pore-forming toxins whose primary action is to lyse midgut epithelial cells in their target insect. In the case of the Cry1A toxins, a prepore oligomeric intermediate is formed after interaction with cadherin receptor. The Cry1A oligomer then interacts with glycosylphosphatidylinositol-anchored receptors. Two Manduca sexta glycosylphosphatidylinositol-anchored proteins, aminopeptidase (APN) and alkaline phosphatase (ALP), have been shown to bind Cry1Ab, although their role in toxicity remains to be determined. Detection of Cry1Ab binding proteins by ligand blot assay revealed that ALP is preferentially expressed earlier during insect development, because it was found in the first larval instars, whereas APN is induced later after the third larval instar. The binding of Cry1Ab oligomer to pure preparations of APN and ALP showed that this toxin structure interacts with both receptors with high affinity (apparent K-d = 0.6 nM), whereas the monomer showed weaker binding (apparent K-d = 101.6 and 267.3 nM for APN and ALP, respectively). Several Cry1Ab nontoxic mutants located in the exposed loop 2 of domain II or in beta-16 of domain III were affected in binding to APN and ALP, depending on their oligomeric state. In particular monomers of the nontoxic domain III, the L511A mutant did not bind ALP but retained APN binding, suggesting that initial interaction with ALP is critical for toxicity. Our data suggest that APN and ALP fulfill two roles. First APN and ALP are initial receptors promoting the localization of toxin monomers in the midgut microvilli before interaction with cadherin. Then APN and ALP function as secondary receptors mediating oligomer insertion into the membrane. However, the expression pattern of these receptors and the phenotype of L511A mutant suggest that ALP may have a predominant role in toxin action because Cry toxins are highly effective against the neonate larvae that is the target for pest control programs.
引用
收藏
页码:12497 / 12503
页数:7
相关论文
共 43 条
[1]   Engineered disulfide bonds increase active-site local stability and reduce catalytic activity of a cold-adapted alkaline phosphatase [J].
Asgeirsson, Bjarni ;
Adalbjornsson, Bjorn Vidar ;
Gylfason, Gudjon Andri .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS, 2007, 1774 (06) :679-687
[2]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[3]   Oligomerization triggers binding of a Bacillus thuringiensis Cry1Ab pore-forming toxin to aminopeptidase N receptor leading to insertion into membrane microdomains [J].
Bravo, A ;
Gómez, I ;
Conde, J ;
Muñoz-Garay, C ;
Sánchez, J ;
Miranda, R ;
Zhuang, M ;
Gill, SS ;
Soberón, M .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2004, 1667 (01) :38-46
[4]   Pore formation activity of Cry1Ab toxin from Bacillus thuringiensis in an improved membrane vesicle preparation from Manduca sexta midgut cell microvilli [J].
Bravo, A ;
Miranda, R ;
Gómez, I ;
Soberón, M .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2002, 1562 (1-2) :63-69
[5]   Mode of action of Bacillus thuringiensis Cry and Cyt toxins and their potential for insect control [J].
Bravo, Alejandra ;
Gill, Sarjeet S. ;
Soberon, Mario .
TOXICON, 2007, 49 (04) :423-435
[6]   Comparison of the localization of Bacillus thuringiensis Cry1A δ-endotoxins and their binding proteins in larval midgut of tobacco hornworm, Manduca sexta [J].
Chen, J ;
Brown, MR ;
Hua, G ;
Adang, MJ .
CELL AND TISSUE RESEARCH, 2005, 321 (01) :123-129
[7]   Structure, diversity, and evolution of protein toxins from spore-forming entomopathogenic bacteria [J].
de Maagd, RA ;
Bravo, A ;
Berry, C ;
Crickmore, N ;
Schnepf, HE .
ANNUAL REVIEW OF GENETICS, 2003, 37 :409-433
[8]   The structure and organization within the membrane of the helices composing the pore-forming domain of Bacillus thuringiensis δ-endotoxin are consistent with an "umbrella-like" structure of the pore [J].
Gazit, E ;
La Rocca, P ;
Sansom, MSP ;
Shai, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (21) :12289-12294
[9]   Transgenic Drosophila reveals a functional in vivo receptor for the Bacillus thuringiensis toxin Cry1Ac1 [J].
Gill, M ;
Ellar, D .
INSECT MOLECULAR BIOLOGY, 2002, 11 (06) :619-625
[10]   Role of receptor interaction in the mode of action of insecticidal Cry and Cyt toxins produced by Bacillus thuringiensis [J].
Gomez, I. ;
Pardo-Lopez, L. ;
Munoz-Garay, C. ;
Fernandez, L. E. ;
Perez, C. ;
Sanchez, J. ;
Soberon, M. ;
Bravo, A. .
PEPTIDES, 2007, 28 (01) :169-173