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. 1996 Jun;111(2):393–401. doi: 10.1104/pp.111.2.393

Protective mechanism of the Mexican bean weevil against high levels of alpha-amylase inhibitor in the common bean.

M Ishimoto 1, M J Chrispeels 1
PMCID: PMC157848  PMID: 8787024

Abstract

Alpha-amylase inhibitor (alpha AI) protects seeds of the common bean (Phaseolus vulgaris) against predation by certain species of bruchids such as the cowpea weevil (Callosobruchus maculatus) and the azuki bean weevil (Callosobruchus chinensis), but not against predation by the bean weevil (Acanthoscelides obtectus) or the Mexican bean weevil (Zabrotes subfasciatus), insects that are common in the Americas. We characterized the interaction of alpha AI-1 present in seeds of the common bean, of a different isoform, alpha AI-2, present in seeds of wild common bean accessions, and of two homologs, alpha AI-Pa present in seeds of the tepary bean (Phaseolus acutifolius) and alpha AI-Pc in seeds of the scarlet runner bean (Phaseolus coccineus), with the midgut extracts of several bruchids. The extract of the Z. subfasciatus larvae rapidly digests and inactivates alpha AI-1 and alpha AI-Pc, but not alpha AI-2 or alpha AI-Pa. The digestion is caused by a serine protease. A single proteolytic cleavage in the beta subunit of alpha AI-1 occurs at the active site of the protein. When degradation is prevented, alpha AI-1 and alpha AI-Pc do not inhibit the alpha-amylase of Z. subfasciatus, although they are effective against the alpha-amylase of C. chinensis. Alpha AI-2 and alpha AI-Pa, on the other hand, do inhibit the alpha-amylase of Z. subfasciatus, suggesting that they are good candidates for genetic engineering to achieve resistance to Z. subfasciatus.

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Selected References

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  1. Altabella T., Chrispeels M. J. Tobacco Plants Transformed with the Bean alphaai Gene Express an Inhibitor of Insect alpha-Amylase in Their Seeds. Plant Physiol. 1990 Jun;93(2):805–810. doi: 10.1104/pp.93.2.805. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Mirkov T. E., Evans S. V., Wahlstrom J., Gomez L., Young N. M., Chrispeels M. J. Location of the active site of the bean alpha-amylase inhibitor and involvement of a Trp, Arg, Tyr triad. Glycobiology. 1995 Feb;5(1):45–50. doi: 10.1093/glycob/5.1.45. [DOI] [PubMed] [Google Scholar]
  3. Mirkov T. E., Wahlstrom J. M., Hagiwara K., Finardi-Filho F., Kjemtrup S., Chrispeels M. J. Evolutionary relationships among proteins in the phytohemagglutinin-arcelin-alpha-amylase inhibitor family of the common bean and its relatives. Plant Mol Biol. 1994 Nov;26(4):1103–1113. doi: 10.1007/BF00040692. [DOI] [PubMed] [Google Scholar]
  4. Moreno J., Altabella T., Chrispeels M. J. Characterization of alpha-Amylase-Inhibitor, a Lectin-Like Protein in the Seeds of Phaseolus vulgaris. Plant Physiol. 1990 Mar;92(3):703–709. doi: 10.1104/pp.92.3.703. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Pratt R. C., Singh N. K., Shade R. E., Murdock L. L., Bressan R. A. Isolation and Partial Characterization of a Seed Lectin from Tepary Bean that Delays Bruchid Beetle Development. Plant Physiol. 1990 Aug;93(4):1453–1459. doi: 10.1104/pp.93.4.1453. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Pueyo J. J., Hunt D. C., Chrispeels M. J. Activation of bean (Phaseolus vulgaris) alpha-amylase inhibitor requires proteolytic processing of the proprotein. Plant Physiol. 1993 Apr;101(4):1341–1348. doi: 10.1104/pp.101.4.1341. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Qian M., Haser R., Payan F. Structure and molecular model refinement of pig pancreatic alpha-amylase at 2.1 A resolution. J Mol Biol. 1993 Jun 5;231(3):785–799. doi: 10.1006/jmbi.1993.1326. [DOI] [PubMed] [Google Scholar]
  8. Schägger H., von Jagow G. Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa. Anal Biochem. 1987 Nov 1;166(2):368–379. doi: 10.1016/0003-2697(87)90587-2. [DOI] [PubMed] [Google Scholar]
  9. Silano V., Furia M., Gianfreda L., Macri A., Palescandolo R., Rab A., Scardi V., Stella E., Valfre F. Inhibition of amylases from different origins by albumins from the wheat kernel. Biochim Biophys Acta. 1975 May 23;391(1):170–178. doi: 10.1016/0005-2744(75)90163-1. [DOI] [PubMed] [Google Scholar]

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