Determination of glucan phosphorylation using heteronuclear 1H, 13C double and 1H, 13C, 31P triple‐resonance NMR spectra. (4th August 2013)

• Record Type: Journal Article
• Authors: Schmieder, Peter; Nitschke, Felix; Steup, Martin; Mallow, Keven; Specker, Edgar
• Is Part Of: Magnetic resonance in chemistry. Volume 51:Number 10(2013:Oct.)
• Page Start: 655
• Page End: 661
• Publication Date: 2013-08-04
• Subjects: Nuclear magnetic resonance spectroscopy -- Periodicals; Chemistry, Organic -- Periodicals; Magnetic resonance -- Periodicals; 538.36
• DOI: 10.1002/mrc.3996
• Languages: English
• ISSNs: 0749-1581

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Phosphorylation and dephosphorylation of starch and glycogen are important for their physicochemical properties and also their physiological functions. It is therefore desirable to reliably determine the phosphorylation sites. Heteronuclear multidimensional NMR‐spectroscopy is in principle a straightforward analytical approach even for complex carbohydrate molecules. With heterogeneous samples from natural sources, however, the task becomes more difficult because a full assignment of the resonances of the carbohydrates is impossible to obtain. Here, we show that the combination of heteronuclear ¹H, ¹³C and ¹H, ¹³C, ³¹P techniques and information derived from spectra of a set of reference compounds can lead to an unambiguous determination of the phosphorylation sites even in heterogeneous samples. Copyright © 2013 John Wiley &amp; Sons, Ltd.</p> </abstract>