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Rapid Communications in Mass Spectrometry

Publication date: 2014-01-01
Volume: 28 Pages: 2191 - 2200
Publisher: John Wiley & Sons

Author:

Verspreet, Joran
Hansen, Anders Holmgaard ; Dornez, Emmie ; Delcour, Jan ; Harrison, Scott James ; Courtin, Christophe

Keywords:

Science & Technology, Life Sciences & Biomedicine, Physical Sciences, Technology, Biochemical Research Methods, Chemistry, Analytical, Spectroscopy, Biochemistry & Molecular Biology, Chemistry, INULIN-TYPE FRUCTANS, MS, POLYMERIZATION, NOMENCLATURE, LEVAN, Carbohydrate Conformation, Carbon Isotopes, Chromatography, Liquid, Fructans, Hexosyltransferases, Models, Molecular, Pachysandra, Plant Proteins, Tandem Mass Spectrometry, 03 Chemical Sciences, 04 Earth Sciences, 06 Biological Sciences, Analytical Chemistry, 31 Biological sciences, 34 Chemical sciences, 37 Earth sciences

Abstract:

RATIONALE: Fructans are carbohydrates predominantly based on fructose which are generally considered to be soluble dietary fibers with health-promoting properties. It is known that the nutritional properties of fructans are affected by their structure. This study focused on structural determination of branched fructans, as the most important dietary fructans are branched graminan-type fructans. METHODS: Branched fructans were synthesized enzymatically by incubation of a heterologously expressed sucrose:fructan 6-fructosyltransferase (6-SFT) from Pachysandra terminalis with native or (13)C-labeled substrates. Liquid chromatography/mass spectrometry (LC/MS) was used for the structural identification of branched fructans. The MS(2) fragmentation of these compounds is described for the first time. Analytes were charged by electrospray ionization in negative mode and a quadrupole mass analyzer was used for MS(2) analysis. RESULTS: The MS(2) fragmentation patterns of branched and linear fructans were shown to differ and distinctive ion formation allowed differentiation between all branched fructan isomers formed. P. terminalis 6-SFT preferred extending the existing fructan branch rather than creating a new branch. CONCLUSIONS: The MS(2) fragmentation patterns described in the current paper now allow rapid screening of large sample sets for the presence of branched, graminan-type fructans. Furthermore, the data enables the characterization of fructan-metabolizing enzymes by identification of the fructan structures produced by in vitro reactions as described here for P. terminalis 6-SFT.