Unambiguous Ex Situ and in Cell 2D ¹³C Solid-State NMR Characterization of Starch and Its Constituents

• Main Authors: Alexandre Poulhazan, Alexandre A. Arnold, Dror E. Warschawski, Isabelle Marcotte
• Format: Article
• Language: English
• Published: MDPI AG 2018-11-01
• Series: International Journal of Molecular Sciences
• Subjects: whole cell NMR; magic-angle spinning; 2D INADEQUATE; crystalline and amorphous starch
• Online Access: https://www.mdpi.com/1422-0067/19/12/3817

Starch is the most abundant energy storage molecule in plants and is an essential part of the human diet. This glucose polymer is composed of amorphous and crystalline domains in different forms (A and B types) with specific physicochemical properties that determine its bioavailability for an organism, as well as its value in the food industry. Using two-dimensional (2D) high resolution solid-state nuclear magnetic resonance (SS-NMR) on ¹³C-labelled starches that were obtained from <i>Chlamydomonas reinhardtii</i> microalgae, we established a complete and unambiguous assignment for starch and its constituents (amylopectin and amylose) in the two crystalline forms and in the amorphous state. We also assigned so far unreported non-reducing end groups and assessed starch chain length, crystallinity and amylose content. Starch was then characterized in situ, i.e., by ¹³C solid-state NMR of intact microalgal cells. Our in-cell methodology also enabled the identification of the effect of nitrogen starvation on starch metabolism. This work shows how solid-state NMR can enable the identification of starch structure, chemical modifications and biosynthesis in situ in intact microorganisms, eliminating time consuming and potentially altering purification steps.