| Literature DB >> 33691770 |
Johannes Zimmermann1, Christoph Kaleta1, Silvio Waschina2,3.
Abstract
Genome-scale metabolic models of microorganisms are powerful frameworks to predict phenotypes from an organism's genotype. While manual reconstructions are laborious, automated reconstructions often fail to recapitulate known metabolic processes. Here we present gapseq ( https://github.com/jotech/gapseq ), a new tool to predict metabolic pathways and automatically reconstruct microbial metabolic models using a curated reaction database and a novel gap-filling algorithm. On the basis of scientific literature and experimental data for 14,931 bacterial phenotypes, we demonstrate that gapseq outperforms state-of-the-art tools in predicting enzyme activity, carbon source utilisation, fermentation products, and metabolic interactions within microbial communities.Entities:
Keywords: Benchmark; Community simulation; Genome-scale metabolic models; Metabolic networks; Metabolic pathway analysis; Metagenome; Microbiome
Mesh:
Year: 2021 PMID: 33691770 PMCID: PMC7949252 DOI: 10.1186/s13059-021-02295-1
Source DB: PubMed Journal: Genome Biol ISSN: 1474-7596 Impact factor: 13.583