代谢途径调控的生物信息学方法:古菌Sulfolobus solfataricus中碳水化合物代谢和TCA循环

B. I. Khayatt
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引用次数: 0

摘要

背景:生物特异性数据库中代谢和基因组信息学的整合需要全面而深入的努力。PathoLogic是Pathway Tools软件包的一个组件,可以从任何生物体的基因组序列和注释文件中创建完整的路径/基因组数据库(PGDBs)。该工具可以使用MetaCyc作为参考知识库来预测代谢途径。这项工作旨在应用生物信息学方法来管理为绿太古菌Sulfolobus solfataricus P2创建的PGDB。这种古菌在80℃和pH 2-4条件下生长最佳。solfataricus P2的全基因组于2001年公布。创建的pgdb通常需要人工管理来填补软件无法检测到的代谢空白。方法:利用Pathway Tools构建黄柳霉P2基因的基因序列。对碳水化合物代谢途径(enterner - doudoroff " ED ")和TCA循环进行生物信息学分析。文献检索以及同源、同源和基于上下文的蛋白质功能预测方法使用Pathway Tools程序的Editors组件。结果:Curation通过添加未被PathoLogic检测到的额外通路来修改数据库中的通路数量。在S. solfataricus P2的PGDB中增加了半磷酸化ED和TCA循环新变异等新途径。在所研究的途径中填补代谢空洞(缺少酶)也参与了管理过程。结论:对S. solfataricus P2的PGDB进行生物信息学管理,完善了数据库,可为其他生物特别是古菌的基因组注释和代谢途径重建提供参考知识基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bioinformatics Approach for Metabolism Pathways Curation: Carbohydrate Metabolism and TCA Cycle in the Archaeon Sulfolobus solfataricus P2
Background: Metabolic and genomic informatics integrations in organism-specific databases require comprehensive and intensive efforts. PathoLogic, a component of the Pathway Tools software package can create complete Pathway/Genome Databases (PGDBs) from genomic sequence and annotation files for any organism. This tool can predict the metabolic pathways using MetaCyc as a reference knowledge base. This work aimed to apply a bioinformatics approach to curate a PGDB created for the Crenarchaeon Sulfolobus solfataricus P2. This archaeon grows optimally at 80o C and pH 2-4. The complete genome of S. solfataricus P2 was released in 2001. Created PGDBs often need manual curations to fill in the metabolic gaps that the software failed to detect. Methods: We used Pathway Tools to create the PGDB for the Sulfolobus solfataricus P2. Bioinformatics curation for carbohydrate metabolism pathway (Entner-Doudoroff “ED”) and TCA cycle was carried out. Literature search as well as homology-, orthology- and context-based protein function prediction methods were followed for this curation using the Editors component of the Pathway Tools program. Results: Curation modified the number of the pathways in the database by adding extra pathways that have not been detected by the PathoLogic. New pathways such as semi-phosphorylated ED and a new variation of the TCA cycle were added to the PGDB of S. solfataricus P2. Filling in the metabolic holes (missing enzymes) in the pathways under study was also involved in the curation process. Conclusion: The bioinformatics curation of the PGDB of S. solfataricus P2 improved the database that can serve as a reference knowledge base for genomic annotations and metabolic pathway reconstructions of other organisms especially the closely related Archaea.
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