Genome-Scale Model Reveals Metabolic Basis of Biomass Partitioning in a Model Diatom
Autor: | Andrew E. Allen, Karen Beeri, Graham Peers, Christopher L. Dupont, Karsten Zengler, Jennifer Levering, Jared T. Broddrick, Joshua Mayers, Bernhard O. Palsson, Alessandra A. Gallina |
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Přispěvatelé: | Ianora, Adrianna |
Rok vydání: | 2016 |
Předmět: |
0301 basic medicine
Chloroplasts Metabolic network lcsh:Medicine Plant Science Endoplasmic Reticulum Biochemistry Genome Models Metabolites Plastids Biomass lcsh:Science Energy-Producing Organelles Secretory Pathway Multidisciplinary biology Genomics Genome project Plants Plankton Lipids Protein subcellular localization prediction Mitochondria Cell Processes Cellular Structures and Organelles Cellular Types Network Analysis Research Article Subcellular Fractions Computer and Information Sciences Algae General Science & Technology Plant Cell Biology Thalassiosira pseudonana Bioenergetics Models Biological Metabolic engineering Metabolic Networks 03 medical and health sciences Plant Cells Genetics Animals Phaeodactylum tricornutum Plastid Diatoms lcsh:R Organisms Biology and Life Sciences Computational Biology Cell Biology Genome Analysis biology.organism_classification Biological Invertebrates Genome Annotation Metabolism 030104 developmental biology Phytoplankton lcsh:Q |
Zdroj: | PloS one, vol 11, iss 5 PLoS ONE, Vol 11, Iss 5, p e0155038 (2016) PLoS ONE |
Popis: | Diatoms are eukaryotic microalgae that contain genes from various sources, including bacteria and the secondary endosymbiotic host. Due to this unique combination of genes, diatoms are taxonomically and functionally distinct from other algae and vascular plants and confer novel metabolic capabilities. Based on the genome annotation, we performed a genome-scale metabolic network reconstruction for the marine diatom Phaeodactylum tricornutum. Due to their endosymbiotic origin, diatoms possess a complex chloroplast structure which complicates the prediction of subcellular protein localization. Based on previous work we implemented a pipeline that exploits a series of bioinformatics tools to predict protein localization. The manually curated reconstructed metabolic network iLB1027_lipid accounts for 1,027 genes associated with 4,456 reactions and 2,172 metabolites distributed across six compartments. To constrain the genome-scale model, we determined the organism specific biomass composition in terms of lipids, carbohydrates, and proteins using Fourier transform infrared spectrometry. Our simulations indicate the presence of a yet unknown glutamine-ornithine shunt that could be used to transfer reducing equivalents generated by photosynthesis to the mitochondria. The model reflects the known biochemical composition of P. tricornutum in defined culture conditions and enables metabolic engineering strategies to improve the use of P. tricornutum for biotechnological applications. |
Databáze: | OpenAIRE |
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