Literature DB >> 20177063

Role of alkaline phosphatase from Manduca sexta in the mechanism of action of Bacillus thuringiensis Cry1Ab toxin.

Iván Arenas1, Alejandra Bravo, Mario Soberón, Isabel Gómez.   

Abstract

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.

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Year:  2010        PMID: 20177063      PMCID: PMC2857145          DOI: 10.1074/jbc.M109.085266

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  42 in total

1.  Cadherin-like receptor binding facilitates proteolytic cleavage of helix alpha-1 in domain I and oligomer pre-pore formation of Bacillus thuringiensis Cry1Ab toxin.

Authors:  Isabel Gómez; Jorge Sánchez; Raúl Miranda; Alejandra Bravo; Mario Soberón
Journal:  FEBS Lett       Date:  2002-02-27       Impact factor: 4.124

Review 2.  Structure, diversity, and evolution of protein toxins from spore-forming entomopathogenic bacteria.

Authors:  Ruud A de Maagd; Alejandra Bravo; Colin Berry; Neil Crickmore; H Ernest Schnepf
Journal:  Annu Rev Genet       Date:  2003       Impact factor: 16.830

3.  Membrane insertion of the Bacillus thuringiensis Cry1Ab toxin: single mutation in domain II block partitioning of the toxin into the brush border membrane.

Authors:  Manoj S Nair; Xinyan Sylvia Liu; Donald H Dean
Journal:  Biochemistry       Date:  2008-05-06       Impact factor: 3.162

4.  A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.

Authors:  M M Bradford
Journal:  Anal Biochem       Date:  1976-05-07       Impact factor: 3.365

5.  Binding of Bacillus thuringiensis Cry1Ac toxin to Manduca sexta aminopeptidase-N receptor is not directly related to toxicity.

Authors:  J L Jenkins; M K Lee; S Sangadala; M J Adang; D H Dean
Journal:  FEBS Lett       Date:  1999-12-03       Impact factor: 4.124

6.  Pore formation activity of Cry1Ab toxin from Bacillus thuringiensis in an improved membrane vesicle preparation from Manduca sexta midgut cell microvilli.

Authors:  Alejandra Bravo; Raúl Miranda; Isabel Gómez; Mario Soberón
Journal:  Biochim Biophys Acta       Date:  2002-05-03

7.  Transgenic Drosophila reveals a functional in vivo receptor for the Bacillus thuringiensis toxin Cry1Ac1.

Authors:  Michael Gill; David Ellar
Journal:  Insect Mol Biol       Date:  2002-12       Impact factor: 3.585

8.  Role of two arginine residues in domain II, loop 2 of Cry1Ab and Cry1Ac Bacillus thuringiensis delta-endotoxin in toxicity and binding to Manduca sexta and Lymantria dispar aminopeptidase N.

Authors:  M K Lee; F Rajamohan; J L Jenkins; A S Curtiss; D H Dean
Journal:  Mol Microbiol       Date:  2000-10       Impact factor: 3.501

9.  Heliothis virescens and Manduca sexta lipid rafts are involved in Cry1A toxin binding to the midgut epithelium and subsequent pore formation.

Authors:  Meibao Zhuang; Daniela I Oltean; Isabel Gómez; Ashok K Pullikuth; Mario Soberón; Alejandra Bravo; Sarjeet S Gill
Journal:  J Biol Chem       Date:  2002-02-08       Impact factor: 5.157

10.  Identification of novel Bacillus thuringiensis Cry1Ac binding proteins in Manduca sexta midgut through proteomic analysis.

Authors:  Rebecca J McNall; Michael J Adang
Journal:  Insect Biochem Mol Biol       Date:  2003-10       Impact factor: 4.714

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  61 in total

1.  Aedes aegypti alkaline phosphatase ALP1 is a functional receptor of Bacillus thuringiensis Cry4Ba and Cry11Aa toxins.

Authors:  Alan I Jiménez; Esmeralda Z Reyes; Angeles Cancino-Rodezno; Leidy P Bedoya-Pérez; Gustavo G Caballero-Flores; Luis F Muriel-Millan; Supaporn Likitvivatanavong; Sarjeet S Gill; Alejandra Bravo; Mario Soberón
Journal:  Insect Biochem Mol Biol       Date:  2012-06-20       Impact factor: 4.714

2.  Cadherin, alkaline phosphatase, and aminopeptidase N as receptors of Cry11Ba toxin from Bacillus thuringiensis subsp. jegathesan in Aedes aegypti.

Authors:  Supaporn Likitvivatanavong; Jianwu Chen; Alejandra Bravo; Mario Soberón; Sarjeet S Gill
Journal:  Appl Environ Microbiol       Date:  2010-10-29       Impact factor: 4.792

Review 3.  Role of pore-forming toxins in bacterial infectious diseases.

Authors:  Ferdinand C O Los; Tara M Randis; Raffi V Aroian; Adam J Ratner
Journal:  Microbiol Mol Biol Rev       Date:  2013-06       Impact factor: 11.056

4.  Specific binding between Bacillus thuringiensis Cry9Aa and Vip3Aa toxins synergizes their toxicity against Asiatic rice borer (Chilo suppressalis).

Authors:  Zeyu Wang; Longfa Fang; Zishan Zhou; Sabino Pacheco; Isabel Gómez; Fuping Song; Mario Soberón; Jie Zhang; Alejandra Bravo
Journal:  J Biol Chem       Date:  2018-06-01       Impact factor: 5.157

5.  Spodoptera frugiperda (J. E. Smith) Aminopeptidase N1 Is a Functional Receptor of the Bacillus thuringiensis Cry1Ca Toxin.

Authors:  Isabel Gómez; Daniel E Rodríguez-Chamorro; Gabriela Flores-Ramírez; Ricardo Grande; Fernando Zúñiga; Francisco J Portugal; Jorge Sánchez; Sabino Pacheco; Alejandra Bravo; Mario Soberón
Journal:  Appl Environ Microbiol       Date:  2018-08-17       Impact factor: 4.792

6.  Domains II and III of Bacillus thuringiensis Cry1Ab toxin remain exposed to the solvent after insertion of part of domain I into the membrane.

Authors:  Luis Enrique Zavala; Liliana Pardo-López; Pablo Emiliano Cantón; Isabel Gómez; Mario Soberón; Alejandra Bravo
Journal:  J Biol Chem       Date:  2011-04-04       Impact factor: 5.157

Review 7.  Receptors of garlic (Allium sativum) lectins and their role in insecticidal action.

Authors:  Santosh K Upadhyay; Pradhyumna K Singh
Journal:  Protein J       Date:  2012-08       Impact factor: 2.371

8.  Enhancement of Bacillus thuringiensis Cry1Ab and Cry1Fa Toxicity to Spodoptera frugiperda by Domain III Mutations Indicates There Are Two Limiting Steps in Toxicity as Defined by Receptor Binding and Protein Stability.

Authors:  Isabel Gómez; Josue Ocelotl; Jorge Sánchez; Christina Lima; Erica Martins; Anayeli Rosales-Juárez; Sotero Aguilar-Medel; André Abad; Hua Dong; Rose Monnerat; Guadalupe Peña; Jie Zhang; Mark Nelson; Gusui Wu; Alejandra Bravo; Mario Soberón
Journal:  Appl Environ Microbiol       Date:  2018-10-01       Impact factor: 4.792

9.  Bacillus thuringiensis Cry1Ab Domain III β-16 Is Involved in Binding to Prohibitin, Which Correlates with Toxicity against Helicoverpa armigera (Lepidoptera: Noctuidae).

Authors:  Igor Henrique Sena da Silva; Isabel Gómez; Sabino Pacheco; Jorge Sánchez; Jie Zhang; Tereza Cristina Luque Castellane; Janete Aparecida Desiderio; Mario Soberón; Alejandra Bravo; Ricardo Antônio Polanczyk
Journal:  Appl Environ Microbiol       Date:  2021-01-04       Impact factor: 4.792

10.  Insecticidal Specificity of Cry1Ah to Helicoverpa armigera Is Determined by Binding of APN1 via Domain II Loops 2 and 3.

Authors:  Zishan Zhou; Yuxiao Liu; Gemei Liang; Yongping Huang; Alejandra Bravo; Mario Soberón; Fuping Song; Xueping Zhou; Jie Zhang
Journal:  Appl Environ Microbiol       Date:  2017-02-01       Impact factor: 4.792

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