Scientific Reports · 2017 · 16 citations · 35 references
Life SciencesBiochemistryMolecular BiologyMetabolismProtein BiochemistryProteomicsFunctional ProteomicsMass Spectrometry Data AnalysisMass Spectrometry-based ProteomicsMicrobial ProteomicsProteomic ProfilingQuantitative ProteomicsAntioxidant PropertiesDevelopmental ProteomicsGluconeogenesisLabel-free ProteomicsLiquid Chromatography-mass SpectrometryLiquid Chromatography-mass Spectrometry AnalysisOxidative Stress In MetabolismUltra-performance Liquid Chromatography-mass Spectrometry
Understanding the initiation and maturing mechanisms is important for rational manipulating sclerotia differentiation and growth from hypha of Polyporus umbellatus. Proteomes in P. umbellatus sclerotia and hyphae at initial, developmental and mature phases were studied. 1391 proteins were identified by nano-liquid chromatograph-mass spectrometry (LC-MS) in Data Dependant Acquisition mode, and 1234 proteins were quantified successfully by Sequential Window Acquisition of all THeoretical fragment ion spectra-MS (SWATH-MS) technology. There were 347 differentially expressed proteins (DEPs) in sclerotia at initial phase compared with those in hypha, and the DEP profiles were dynamically changing with sclerotia growth. Oxidative stress (OS) in sclerotia at initial phase was indicated by the repressed proteins of respiratory chain, tricarboxylic acid cycle and the activation of glycolysis/gluconeogenesis pathways were determined based on DEPs. The impact of glycolysis/gluconeogenesis on sclerotium induction was further verified by glycerol addition assays, in which 5% glycerol significantly increased sclerotial differentiation rate and biomass. It can be speculated that OS played essential roles in triggering sclerotia differentiation from hypha of P. umbellatus, whereas antioxidant activity associated with glycolysis is critical for sclerotia growth. These findings reveal a mechanism for sclerotial differentiation in P. umbellatus, which may also be applicable for other fungi.
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