Computational identification and characterization of chitinase 1 and chitinase 2 from neotropical isolates of .

Front Bioinform

Laboratorio de Bioinformática Aplicada, Escuela de Ciencias Biológicas, Universidad Nacional de Costa Rica, Heredia, Costa Rica.

Published: October 2024

AI Article Synopsis

  • - The study focuses on the genetic analysis of chitinase enzymes from neotropical fungal isolates, which are important for agricultural biological control due to their ability to break down chitin, a component of insect exoskeletons and fungal cell walls.
  • - Researchers examined eight genomes, discovering eleven chitinase 1 genes categorized into two types and highlighting variations particularly in chitinase 1, which may indicate different roles in infection and growth processes.
  • - The findings stress the significance of local fungal genomes in understanding pathogen-host interactions and suggest practical agricultural applications, emphasizing the need for more experimental work to validate these computational insights.

Article Abstract

Background: The fungus is widely used for agronomical applications, mainly in biological control. uses chitinase enzymes to degrade chitin, a major chemical component found in insect exoskeletons and fungal cell walls. However, until recently, genomic information on neotropical isolates, as well as their metabolic and biotechnological potential, has been limited.

Methods: Eight complete genomes of Neotropical origin and three references were studied to identify chitinase genes and its corresponding proteins, which were curated and characterized using manual curation and computational tools. We conducted a computational study to highlight functional differences and similarities for chitinase proteins in these Neotropical isolates.

Results: Eleven chitinase 1 genes were identified, categorized as chitinase 1.1 and chitinase 1.2. Five chitinase 2 genes were identified but presented a higher sequence conservation across all sequences. Interestingly, physicochemical parameters were more similar between chitinase 1.1 and chitinase 2 than between chitinase 1.1 and 1.2.

Conclusion: Chitinases 1 and 2 demonstrated variations, especially within chitinase 1, which presented a potential paralog. These differences were observed in their physical parameters. Additionally, CHIT2 completely lacks a signal peptide. This implies that CHIT1 might be associated with infection processes, while CHIT2 could be involved in morphogenesis and cellular growth. Therefore, our work highlights the importance of computational studies on local isolates, providing valuable resources for further experimental validation. Intrinsic changes within local species can significantly impact our understanding of complex pathogen-host interactions and offer practical applications, such as biological control.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11527780PMC
http://dx.doi.org/10.3389/fbinf.2024.1434442DOI Listing

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