Novel Metabolic Pathways and Regulons for Hexuronate Utilization in Proteobacteria
| العنوان: | Novel Metabolic Pathways and Regulons for Hexuronate Utilization in Proteobacteria |
|---|---|
| المؤلفون: | Nawar Al-Obaidi, Salehe Ghasempur, Dmitry A. Rodionov, John A. Gerlt, Matthew W. Vetting, Irina A. Rodionova, Natalia V. Sernova, Jason T. Bouvier, Steven C. Almo |
| المصدر: | Journal of Bacteriology. 201 |
| بيانات النشر: | American Society for Microbiology, 2019. |
| سنة النشر: | 2019 |
| مصطلحات موضوعية: | Comparative genomics, 0303 health sciences, 030306 microbiology, Hexuronic Acids, Computational Biology, Context (language use), Computational biology, Biology, biology.organism_classification, Regulon, Microbiology, Comamonadaceae, 03 medical and health sciences, Metabolic pathway, Halomonadaceae, Proteobacteria, Hexuronate, Molecular Biology, Gene, Metabolic Networks and Pathways, Research Article, 030304 developmental biology |
| الوصف: | We used comparative genomics to reconstruct d-galacturonic and d-glucuronic acid catabolic pathways and associated transcriptional regulons involving the tripartite ATP-independent periplasmic (TRAP) family transporters that bind hexuronates in proteobacteria. The reconstructed catabolic network involves novel transcription factors, catabolic enzymes, and transporters for utilization of both hexuronates and aldarates (d-glucarate and meso-galactarate). The reconstructed regulons for a novel GntR family transcription factor, GguR, include the majority of hexuronate/aldarate utilization genes in 47 species from the Burkholderiaceae, Comamonadaceae, Halomonadaceae, and Pseudomonadaceae families. GudR, GulR, and UdhR are additional local regulators of some hexuronate/aldarate utilization genes in some of the above-mentioned organisms. The predicted DNA binding motifs of GguR and GudR regulators from Ralstonia pickettii and Polaromonas were validated by in vitro binding assays. Genes from the GulR- and GguR-controlled loci were differentially expressed in R. pickettii grown on hexuronates and aldarates. By a combination of bioinformatics and experimental techniques we identified a novel variant of the oxidative pathway for hexuronate utilization, including two previously uncharacterized subfamilies of lactone hydrolases (UxuL and UxuF). The genomic context of respective genes and reconstruction of associated pathways suggest that both enzymes catalyze the conversion of d-galactaro- and d-glucaro-1,5-lactones to the ring-opened aldarates. The activities of the purified recombinant enzymes, UxuL and UxuF, from four proteobacterial species were directly confirmed and kinetically characterized. The inferred novel aldarate-specific transporter from the tripartite tricarboxylate transporter (TTT) family transporter TctC was confirmed to bind d-glucarate in vitro. This study expands our knowledge of bacterial carbohydrate catabolic pathways by identifying novel families of catabolic enzymes, transcriptional regulators, and transporters. IMPORTANCE Hexuronate catabolic pathways and their transcriptional networks are highly variable among different bacteria. We identified novel transcriptional regulators that control the hexuronate and aldarate utilization genes in four families of proteobacteria. By regulon reconstruction and genome context analysis we identified several novel components of the common hexuronate/aldarate utilization pathways, including novel uptake transporters and catabolic enzymes. Two novel families of lactonases involved in the oxidative pathway of hexuronate catabolism were characterized. Novel transcriptional regulons were validated via in vitro binding assays and gene expression studies with Polaromonas and Ralstonia species. The reconstructed catabolic pathways are interconnected with each other metabolically and coregulated via the GguR regulons in proteobacteria. |
| تدمد: | 1098-5530 0021-9193 |
| URL الوصول: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75763750a64f8b3667e955c6bfeb5e45 https://doi.org/10.1128/jb.00431-18 |
| حقوق: | OPEN |
| رقم الأكسشن: | edsair.doi.dedup.....75763750a64f8b3667e955c6bfeb5e45 |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 10985530 00219193 |
|---|