Integrated analysis of zone-specific protein and metabolite profiles within nitrogen-fixing Medicago truncatula-Sinorhizobium medicae nodules

• Published in: PloS one 2017-07, Vol.12 (7), p.e0180894-e0180894
• Main Authors: Ogden, Aaron J, Gargouri, Mahmoud, Park, JeongJin, Gang, David R, Kahn, Michael L
• Format: Article
• Language: English
• Subjects: Abundance; Alfalfa; Amino acids; Bacteria; Bacterial infections; Bacteroids; Barrels; BASIC BIOLOGICAL SCIENCES; Biology and Life Sciences; Biosynthesis; Carbon; Chromatography; Dicarboxylic acids; Enzymes; Fatty acids; Fatty Acids - metabolism; Gas chromatography; Gene Expression Regulation, Plant - physiology; Glycolysis; Infections; Legumes; Localization; Mass spectrometry; Mass spectroscopy; Medicago truncatula - metabolism; Metabolism; Metabolites; Nitrogen; Nitrogen - metabolism; Nitrogen fixation; Nitrogen Fixation - physiology; Nodules; Organs; Physical Sciences; Plant Roots - microbiology; Plant sciences; Principal components analysis; Proteins; Root nodules; Root Nodules, Plant; Scientific imaging; Sinorhizobium - metabolism; Spatial discrimination; Symbionts; Symbiosis; Tandem Mass Spectrometry
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0180894

Symbiotic nitrogen fixation (SNF) between rhizobia and legumes requires metabolic coordination within specialized root organs called nodules. Nodules formed in the symbiosis between S. medicae and barrel medic (M. truncatula) are indeterminate, cylindrical, and contain spatially distinct developmental zones. Bacteria in the infection zone II (ZII), interzone II-III (IZ), and nitrogen fixation zone III (ZIII) represent different stages in the metabolic progression from free-living bacteria into nitrogen fixing bacteroids. To better understand the coordination of plant and bacterial metabolism within the nodule, we used liquid and gas chromatography coupled to tandem mass spectrometry (MS) to observe protein and metabolite profiles representative of ZII, IZ, ZIII, whole-nodule, and primary root. Our MS-based approach confidently identified 361 S. medicae proteins and 888 M. truncatula proteins, as well as 160 metabolites from each tissue. The data are consistent with several organ- and zone-specific protein and metabolite localization patterns characterized previously. We used our comprehensive dataset to demonstrate how multiple branches of primary metabolism are coordinated between symbionts and zones, including central carbon, fatty acid, and amino acid metabolism. For example, M. truncatula glycolysis enzymes accumulate from zone I to zone III within the nodule, while equivalent S. medicae enzymes decrease in abundance. We also show the localization of S. medicae's transition to dicarboxylic acid-dependent carbon metabolism within the IZ. The spatial abundance patterns of S. medicae fatty acid (FA) biosynthesis enzymes indicate an increased demand for FA production in the IZ and ZIII as compared to ZI. These observations provide a resource for those seeking to understand coordinated physiological changes during the development of SNF.