计算鉴定和表征来自新热带贝维氏菌分离物的几丁质酶 1 和几丁质酶 2。

IF 2.8 Q2 MATHEMATICAL & COMPUTATIONAL BIOLOGY
Frontiers in bioinformatics Pub Date : 2024-10-18 eCollection Date: 2024-01-01 DOI:10.3389/fbinf.2024.1434442
Juan Segura-Vega, Allan González-Herrera, Ramón Molina-Bravo, Stefany Solano-González
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引用次数: 0

摘要

背景:真菌 Beauveria bassiana 被广泛应用于农学领域,主要是生物防治。B. bassiana 利用几丁质酶降解几丁质,几丁质是昆虫外骨骼和真菌细胞壁中的主要化学成分。然而,直到最近,有关新热带分离菌的基因组信息及其代谢和生物技术潜力还很有限:方法:我们研究了 8 个新热带地区的完整 B. bassiana 基因组和 3 个参考文献,以确定几丁质酶基因及其相应的蛋白质,并使用人工整理和计算工具对这些基因组进行了整理和特征描述。我们进行了一项计算研究,以突出这些新热带分离株中几丁质酶蛋白的功能差异和相似性:结果:确定了 11 个几丁质酶 1 基因,分为几丁质酶 1.1 和几丁质酶 1.2。发现了 5 个几丁质酶 2 基因,但在所有序列中呈现出较高的序列保守性。有趣的是,与几丁质酶 1.1 和 1.2 相比,几丁质酶 1.1 和几丁质酶 2 的理化参数更为相似:几丁质酶 1 和 2 显示出了差异,尤其是几丁质酶 1,它是一个潜在的旁系亲属。这些差异体现在它们的物理参数上。此外,CHIT2 完全缺乏信号肽。这意味着 CHIT1 可能与感染过程有关,而 CHIT2 可能参与形态发生和细胞生长。因此,我们的工作凸显了对本地分离物进行计算研究的重要性,为进一步的实验验证提供了宝贵的资源。本地物种的内在变化会极大地影响我们对复杂的病原体-宿主相互作用的理解,并提供实际应用,如生物防治。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Computational identification and characterization of chitinase 1 and chitinase 2 from neotropical isolates of Beauveria bassiana.

Background: The fungus Beauveria bassiana is widely used for agronomical applications, mainly in biological control. B. bassiana 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 B. bassiana 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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