Absolute quantification of Medicago truncatula sucrose synthase isoforms and N-metabolism enzymes in symbiotic root nodules and the detection of novel nodule phosphoproteins by mass spectrometry

Mass spectrometry (MS) has become increasingly important for tissue specific protein quantification at the isoform level, as well as for the analysis of protein post-translational regulation mechanisms and turnover rates. Thanks to the development of high accuracy mass spectrometers, peptide sequenc...

Ausführliche Beschreibung

Bibliographische Detailangaben
Veröffentlicht in:Journal of experimental botany. - 1985. - 59(2008), 12 vom: 01., Seite 3307-15
1. Verfasser: Wienkoop, Stefanie (VerfasserIn)
Weitere Verfasser: Larrainzar, Estíbaliz, Glinski, Mirko, González, Esther M, Arrese-Igor, Cesar, Weckwerth, Wolfram
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2008
Zugriff auf das übergeordnete Werk:Journal of experimental botany
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Phosphoproteins Plant Proteins Protein Isoforms Glucosyltransferases EC 2.4.1.- sucrose synthase EC 2.4.1.13 Nitrogen N762921K75
LEADER 01000naa a22002652 4500
001 NLM182245047
003 DE-627
005 20231223162550.0
007 cr uuu---uuuuu
008 231223s2008 xx |||||o 00| ||eng c
024 7 |a 10.1093/jxb/ern182  |2 doi 
028 5 2 |a pubmed24n0608.xml 
035 |a (DE-627)NLM182245047 
035 |a (NLM)18772307 
040 |a DE-627  |b ger  |c DE-627  |e rakwb 
041 |a eng 
100 1 |a Wienkoop, Stefanie  |e verfasserin  |4 aut 
245 1 0 |a Absolute quantification of Medicago truncatula sucrose synthase isoforms and N-metabolism enzymes in symbiotic root nodules and the detection of novel nodule phosphoproteins by mass spectrometry 
264 1 |c 2008 
336 |a Text  |b txt  |2 rdacontent 
337 |a ƒaComputermedien  |b c  |2 rdamedia 
338 |a ƒa Online-Ressource  |b cr  |2 rdacarrier 
500 |a Date Completed 27.10.2008 
500 |a Date Revised 20.10.2021 
500 |a published: Print 
500 |a Citation Status MEDLINE 
520 |a Mass spectrometry (MS) has become increasingly important for tissue specific protein quantification at the isoform level, as well as for the analysis of protein post-translational regulation mechanisms and turnover rates. Thanks to the development of high accuracy mass spectrometers, peptide sequencing without prior knowledge of the amino acid sequence--de novo sequencing--can be performed. In this work, absolute quantification of a set of key enzymes involved in carbon and nitrogen metabolism in Medicago truncatula 'Jemalong A17' root nodules is presented. Among them, sucrose synthase (SuSy; EC 2.4.1.13), one of the central enzymes in sucrose cleavage in root nodules, has been further characterized and the relative phosphorylation state of the three most abundant isoforms has been quantified. De novo sequencing provided sequence information of a so far unidentified peptide, most probably belonging to SuSy2, the second most abundant isoform in M. truncatula root nodules. TiO(2)-phosphopeptide enrichment led to the identification of not only a phosphorylation site at Ser11 in SuSy1, but also of several novel phosphorylation sites present in other root nodule proteins such as alkaline invertase (AI; EC 3.2.1.26) and an RNA-binding protein 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 7 |a Phosphoproteins  |2 NLM 
650 7 |a Plant Proteins  |2 NLM 
650 7 |a Protein Isoforms  |2 NLM 
650 7 |a Glucosyltransferases  |2 NLM 
650 7 |a EC 2.4.1.-  |2 NLM 
650 7 |a sucrose synthase  |2 NLM 
650 7 |a EC 2.4.1.13  |2 NLM 
650 7 |a Nitrogen  |2 NLM 
650 7 |a N762921K75  |2 NLM 
700 1 |a Larrainzar, Estíbaliz  |e verfasserin  |4 aut 
700 1 |a Glinski, Mirko  |e verfasserin  |4 aut 
700 1 |a González, Esther M  |e verfasserin  |4 aut 
700 1 |a Arrese-Igor, Cesar  |e verfasserin  |4 aut 
700 1 |a Weckwerth, Wolfram  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Journal of experimental botany  |d 1985  |g 59(2008), 12 vom: 01., Seite 3307-15  |w (DE-627)NLM098182706  |x 1460-2431  |7 nnns 
773 1 8 |g volume:59  |g year:2008  |g number:12  |g day:01  |g pages:3307-15 
856 4 0 |u http://dx.doi.org/10.1093/jxb/ern182  |3 Volltext 
912 |a GBV_USEFLAG_A 
912 |a SYSFLAG_A 
912 |a GBV_NLM 
912 |a GBV_ILN_350 
951 |a AR 
952 |d 59  |j 2008  |e 12  |b 01  |h 3307-15