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Zorrilla, F.

Publications and source records attributed to Zorrilla, F..

3 recordsLinked to original sources

Reconstruction of genome-scale metabolic model for Hansenula polymorpha using RAVEN toolbox

Genome scale metabolic models (GEMs) provide a useful framework for modeling the metabolism of microorganisms. While the applications of GEMs are wide and far reaching, the reconstruction and continuous curation of such models can be perceived as a tedious and time consuming task. Using the RAVEN toolbox, this protocol practically demonstrates how researchers can create their own GEMs using a homology based approach. To provide a complete example, we reconstruct a draft GEM for the industrially relevant yeast Hansenula polymorpha.

systems biology

metaGEM: reconstruction of genome scale metabolic models directly from metagenomes.

Advances in genome-resolved metagenomic analysis of complex microbial communities have revealed a large degree of interspecies and intraspecies genetic diversity through the reconstruction of metagenome assembled genomes (MAGs). Yet, metabolic modeling efforts still tend to rely on reference genomes as the starting point for reconstruction and simulation of genome scale metabolic models (GEMs), neglecting the immense intra- and inter-species diversity present in microbial communities. Here we present metaGEM (https://github.com/franciscozorrilla/metaGEM), an end-to-end highly scalable pipeline enabling metabolic modeling of multi-species communities directly from metagenomic samples. The pipeline automates all steps from the extraction of context-specific prokaryotic GEMs from metagenome assembled genomes to community level flux balance simulations. To demonstrate the capabilities of the metaGEM pipeline, we analyzed 483 samples spanning lab culture, human gut, plant associated, soil, and ocean metagenomes, to reconstruct over 14 000 prokaryotic GEMs. We show that GEMs reconstructed from metagenomes have fully represented metabolism comparable to the GEMs reconstructed from reference genomes. We further demonstrate that metagenomic GEMs capture intraspecies metabolic diversity by identifying the differences between pathogenicity levels of type 2 diabetes at the level of gut bacterial metabolic exchanges. Overall, our pipeline enables simulation-ready metabolic model reconstruction directly from individual metagenomes, provides a resource of all reconstructed metabolic models, and showcases community-level modeling of microbiomes associated with disease conditions allowing generation of mechanistic hypotheses.

bioinformatics

Plastic-degrading potential across the global microbiome correlates with recent pollution trends

Poor recycling has accumulated millions of tons of plastic waste in terrestrial and marine environments. While biodegradation is a plausible route towards sustainable management of plastic waste, the global diversity of plastic-degrading enzymes remains poorly understood. Taking advantage of global environmental DNA sampling projects, here we construct HMM models from experimentally-verified enzymes and mine ocean and soil metagenomes to assess the global potential of microorganisms to degrade plastics. By controlling for false positives using gut microbiome data, we compile a catalogue of over 30,000 non-redundant enzyme homologues with the potential to degrade 10 different plastic types. While differences between the ocean and soil microbiomes likely reflect the base compositions of these environments, we find that ocean enzyme abundance might increase with depth as a response to plastic pollution and not merely taxonomic composition. By obtaining further pollution measurements, we reveal that the abundance of the uncovered enzymes in both ocean and soil habitats significantly correlates with marine and country-specific plastic pollution trends. Our study thus uncovers the earth microbiomes potential to degrade plastics, providing evidence of a measurable effect of plastic pollution on the global microbial ecology as well as a useful resource for further applied research.

bioinformatics