000061658 001__ 61658 000061658 005__ 20190625111504.0 000061658 0247_ $$2DOI$$a10.1080/00032710802162442 000061658 0247_ $$2WOS$$aWOS:000258079500006 000061658 0247_ $$2altmetric$$aaltmetric:3398899 000061658 037__ $$aPreJuSER-61658 000061658 041__ $$aeng 000061658 082__ $$a540 000061658 084__ $$2WoS$$aChemistry, Analytical 000061658 1001_ $$0P:(DE-Juel1)VDB71401$$aFitri, N.$$b0$$uFZJ 000061658 245__ $$aMolybdenum speciation in raw phloem sap of castor bean 000061658 260__ $$aNew York, NY$$bTaylor & Francis$$c2008 000061658 300__ $$a1773 - 1784 000061658 3367_ $$0PUB:(DE-HGF)16$$2PUB:(DE-HGF)$$aJournal Article 000061658 3367_ $$2DataCite$$aOutput Types/Journal article 000061658 3367_ $$00$$2EndNote$$aJournal Article 000061658 3367_ $$2BibTeX$$aARTICLE 000061658 3367_ $$2ORCID$$aJOURNAL_ARTICLE 000061658 3367_ $$2DRIVER$$aarticle 000061658 440_0 $$07961$$aAnalytical Letters$$v41$$x0003-2719$$y10 000061658 500__ $$aRecord converted from VDB: 12.11.2012 000061658 520__ $$aSeparation and quantification of molybdenum (Mo) in raw phloem sap from castor bean (Ricinus communis L.) was performed by size exclusion chromatography (SEC) and further purification was performed using quantitative preparative native continuous polyacrylamide gel electrophoresis (QPNC-PAGE). For elemental detection, an inductively coupled plasma quadrupole mass spectrometer (ICP-QMS) was applied. Two different SEC columns were utilized: column A, Sephadex G-50 SF (700mm24mm), and column B, Sephadex G-25 M (28mm9mm). The protein content of the fractions was determined by the Bradford method. Using column A, two peaks of Mo were detected consisting of a main peak (MoA2) in the low molecular weight area (1.35 kDa), and a minor peak (MoA1,30 kDa) at the void volume of the column. Both Mo species were detected at the ultraviolet (UV) active absorption area of raw phloem sap. Two peaks of Mo were also detected using column B, the first peak (MoB1) being at the same elution volume as the protein of raw phloem sap, and the second one (MoB2) was eluted in the area of 1.5 to 2.4mL of elution volume. Raw phloem sap digested by proteinase K-enzyme indicates a significant reduction of MoB1 peak, which suggests that the peak may contain Mo bound to protein or polypeptides. The raw phloem sap and SEC fraction containing highest Mo concentration (MoA2) were furthermore separated by QPNC-PAGE. The result reveals that the Mo-containing fraction from the raw phloem sap was eluted at the same retention volume as the purified sample. This implies that the Mo species were also successfully separated and purified using QPNC-PAGE. 000061658 536__ $$0G:(DE-Juel1)FUEK407$$2G:(DE-HGF)$$aTerrestrische Umwelt$$cP24$$x0 000061658 588__ $$aDataset connected to Web of Science 000061658 650_7 $$2WoSType$$aJ 000061658 65320 $$2Author$$acastor bean 000061658 65320 $$2Author$$aMo speciation 000061658 65320 $$2Author$$aphloem sap 000061658 65320 $$2Author$$aQPNC-PAGE 000061658 65320 $$2Author$$aSEC 000061658 7001_ $$0P:(DE-Juel1)129343$$aKastenholz, B.$$b1$$uFZJ 000061658 7001_ $$0P:(DE-HGF)0$$aBuchari, B.$$b2 000061658 7001_ $$0P:(DE-HGF)0$$aAmran, M. B.$$b3 000061658 7001_ $$0P:(DE-HGF)0$$aWarganegara, F. M.$$b4 000061658 773__ $$0PERI:(DE-600)2098207-0$$a10.1080/00032710802162442$$gVol. 41, p. 1773 - 1784$$p1773 - 1784$$q41<1773 - 1784$$tAnalytical letters$$v41$$x0003-2719$$y2008 000061658 8567_ $$uhttp://dx.doi.org/10.1080/00032710802162442 000061658 909CO $$ooai:juser.fz-juelich.de:61658$$pVDB 000061658 9131_ $$0G:(DE-Juel1)FUEK407$$bErde und Umwelt$$kP24$$lTerrestrische Umwelt$$vTerrestrische Umwelt$$x0 000061658 9141_ $$y2008 000061658 915__ $$0StatID:(DE-HGF)0010$$aJCR/ISI refereed 000061658 9201_ $$0I:(DE-Juel1)ICG-3-20090406$$d31.10.2010$$gICG$$kICG-3$$lPhytosphäre$$x1 000061658 970__ $$aVDB:(DE-Juel1)97020 000061658 980__ $$aVDB 000061658 980__ $$aConvertedRecord 000061658 980__ $$ajournal 000061658 980__ $$aI:(DE-Juel1)IBG-2-20101118 000061658 980__ $$aUNRESTRICTED 000061658 981__ $$aI:(DE-Juel1)IBG-2-20101118 000061658 981__ $$aI:(DE-Juel1)ICG-3-20090406