The Bark Beetle (Curculionidae: Scolytinae) Has Digestive Capacity to Degrade Complex Substrates: Functional Characterization and Heterologous Expression of an α-Amylase.

Int J Mol Sci

Laboratorio de Variación Biológica y Evolución, Departamento de Zoología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Prolongación de Carpio y Plan de Ayala s/n, Santo Tomás, Miguel Hidalgo, Mexico City 11340, Mexico.

Published: December 2020

AI Article Synopsis

  • - Bark beetles play a crucial role in coniferous forests by helping with regeneration, succession, and material recycling by colonizing and killing stressed or damaged pine trees.
  • - The study focused on understanding a specific α-amylase enzyme (AmyDr) found in these beetles, which helps them digest starch; it identified a gene coding for a protein that has a unique mutation affecting its binding sites.
  • - Results showed that the enzyme displayed higher activity in the gut compared to other body parts, suggesting that starch digestion is primarily done in the midgut, with its activity influenced by the beetle's developmental stages and starch availability in their host trees.

Article Abstract

-bark beetles are natural agents contributing to vital processes in coniferous forests, such as regeneration, succession, and material recycling, as they colonize and kill damaged, stressed, or old pine trees. These beetles spend most of their life cycle under stem and roots bark where they breed, develop, and feed on phloem. This tissue is rich in essential nutrients and complex molecules such as starch, cellulose, hemicellulose, and lignin, which apparently are not available for these beetles. We evaluated the digestive capacity of to hydrolyze starch. Our aim was to identify α-amylases and characterize them both molecularly and biochemically. The findings showed that . has an α-amylase gene () with a single isoform, and ORF of 1452 bp encoding a 483-amino acid protein (53.15 kDa) with a predicted signal peptide of 16 amino acids. AmyDr has a mutation in the chlorine-binding site, present in other phytophagous insects and in a marine bacterium. Docking analysis showed that AmyDr presents a higher binding affinity to amylopectin compared to amylose, and an affinity binding equally stable to calcium, chlorine, and nitrate ions. AmyDr native protein showed amylolytic activity in the head-pronotum and gut, and its recombinant protein, a polypeptide of ~53 kDa, showed conformational stability, and its activity is maintained both in the presence and absence of chlorine and nitrate ions. The gene showed a differential expression significantly higher in the gut than the head-pronotum, indicating that starch hydrolysis occurs mainly in the midgut. An overview of the gene expression suggests that the amylolytic activity is regulated through the developmental stages of this bark beetle and associated with starch availability in the host tree.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7792934PMC
http://dx.doi.org/10.3390/ijms22010036DOI Listing

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