Journal of the Science of Food and Agriculture · 2012 · 15 citations · 27 references
Life SciencesBiochemistryMolecular BiologyMass Spectrometric AnalysisPlant Molecular BiologyProteomicsMass SpectrometryMass Spectrometry-based ProteomicsPeptide AnalysisPeptide IdentificationProtein AnalysisProtein Sequence AnalysisCdna CloningCdna Library ConstructionMaldi-tof Mass SpectrometryMass Spectrometric IdentificationMass Spectrometry-based IdentificationMatrix-assisted Laser Desorption Ionization Time-of-flight Mass SpectrometryMatrix-assisted Laser Desorption/ionizationMatrix-assisted Laser Desorption/ionization Time-of-flight Mass Spectrometry
BACKGROUND: Dioscorins are the major storage proteins of yam tubers. However, the molecular nature of their heterogeneity in tubers has not been fully elucidated. In this study the authors isolated the dioscorin gene families of Dioscorea japonica and Dioscorea pseudojaponica, performed matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry (MALDI-TOF-MS) and elucidated which dioscorin isoforms are the major constituents in tubers. RESULTS: The dioscorin gene families of D. japonica (Dj-dioA1-Dj-dioA4, Dj-dioB1 and Dj-dioB2) and D. pseudojaponica (Dp-dioA1-Dp-dioA5 and Dp-dioB1) were cloned from cDNA libraries of yam tubers. The dioscorins isolated from Dioscorea alata (Da-dioscorins), D. japonica (Dj-dioscorins) and D. pseudojaponica (Dp-dioscorins) were mainly monomers, with a few dimers. The monomers contained one intramolecular disulfide bond (Cys(28)-Cys(187)) and belonged to Class A dioscorins with two cysteine residues. The dimers consisted of Class B dioscorins with one intermolecular disulfide bond (Cys(40)-Cys(40)). Results of MALDI-TOF-MS revealed that the Da-dioscorins were mainly encoded by Da-dioA2, Da-dioA3 and Da-dioA4. The majority of the Dj-dioscorins were encoded by Dj-dioA1, Dj-dioA2, Dj-dioA3 and Dj-dioB2. The Dp-dioscorins mainly comprised proteins encoded by Dp-dioA1, Dp-dioA3, Dp-dioA4, Dp-dioB1 and Dp-dioB2. CONCLUSION: Determination of the constituents of dioscorin isoforms in yam tubers provides a basis for future studies of their physiological and biomedical functions.
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Specific reduction of wheat storage proteins by thioredoxin h.
Kàroly Kobrehel, Joshua Wong, Árpád Balogh et al. · PLANT PHYSIOLOGY · 1992 · 195 citations · Full text
Feng‐Lin Hsu, Yaw-Huei Lin, Mei‐Hsien Lee et al. · Journal of Agricultural and Food Chemistry · 2002 · 97 citations