Characterisation of soluble and insoluble cell wall fractions from rye, wheat and hull-less barley endosperm flours

Within cereal endosperm flours, arabinoxylan and β-glucan molecules exist in either a soluble or an insoluble form. From a nutritional functionality viewpoint, soluble and insoluble forms offer different potential health advantages, so it is important to define both the features controlling solubilisation and the properties of each of the soluble and insoluble fractions. Factors known to affect the stability of arabinoxylan (AX) and β-glucan (BG) solutions include AX branching extent and type, and the ratio of cellotriose to cellotetraose units (DP3/DP4) in BG. Through studying the solubilisation of AX and BG from wheat, rye, and hull less barley endosperm under conditions that avoid the use of alkali or ethanol during the solubilisation process, we report (a) similar A/X ratios and fine structures for extracted soluble arabinoxylan and the corresponding insoluble AX within the cell walls for rye and wheat endosperm flours, (b) comparable DP3/DP4 ratios for soluble β-glucan, flour and insoluble β-glucan within the endosperm cell wall of hull less barley, and (c) evidence for enrichment of β-glucan at the exterior of residual insoluble cell walls. Therefore, the factors determining solubilisation of AX and BG from endosperm cell walls are different to those that determine the stability of aqueous solutions of the same polymers, and β-glucan may show limited solubilisation by being trapped within restraining cross-linked arabinoxylans in the cell wall

Effects of diverse food processing conditions on the structure and solubility of wheat, barley and rye endosperm dietary fibre

The effects of archetypal food processing conditions (dough formation, baking, extrusion, and cooking/boiling) on dietary fibre structure and extractability from the endosperm flours of rye, hull less barley and wheat are reported. For all flours and processes, the distributions of soluble/insoluble cell wall dietary fibre as well as the chemical composition (arabinoxylan (AX) branching patterns, β-glucan DP3/DP4 (DP = degree of polymerisation) ratios) of solubilised fractions were characterised. The results show that overall the total amounts of AX and β-glucan (BG) were not significantly affected by processing but that there were similar increases in the soluble fibre fraction (20-29%) for baked, extruded, and boiled/cooked processes for each flour, with lower (10-15%) increases for all flours processed into dough. In all cases, solubilised fractions of AX and BG had very similar chemical structures to the starting flour, suggesting that increased solubilisation was not due to specific chemical fractions. Confocal images illustrate loosely-held associations of β-glucan with the cell walls of processed foods in contrast to some of the arabinoxylans which appear more tightly held within the residual cell walls. The similarities in behaviour across the three grains are consistent with mechanical treatments during food preparation resulting in similar extents of disentanglement of physically-constrained AX and BG leading to their partial solubilisation

In vitro fermentation gas kinetics and end-products of soluble and insoluble cereal flour dietary fibres are similar

Insoluble dietary fibre is often considered to be fermented slower and to a lesser extent in (models for) the colon than soluble dietary fibre. However these comparisons are typically made for fibre components of different composition. In the case of fibre from refined cereal flours, there is little difference in fibre composition between soluble and insoluble forms, so effects of solubility on fermentation can be tested without this confounding factor. For each of wheat, rye, and hull-less barley, soluble and insoluble fibre fractions from refined flour and models for baking and extrusion had comparable in vitro fermentation rates and extents, with similar levels of short chain fatty acid metabolites. This study suggests that there should be little difference in the large intestinal nutritional functionality of the soluble and insoluble fibre fractions from cereal grain flours, either unprocessed or after baking or extrusion processing

Separation and purification of soluble polymers and cell wall fractions from wheat, rye and hull less barley endosperm flours for structure-nutrition studies

The nutritional values associated with the cell walls of cereal endosperm flours are due to a combination of solubilized arabinoxylan and (1-3,1-4)-β-d-glucan as well as residual nonsolubilized cell wall material. In order to investigate structure-nutrition relationships, an appropriate method for the complete functional and structural characterization of cell wall polysaccharides in various cereal endosperm flours is described. This involves the separation of soluble polymers and the residual cell wall fraction without using organic solvents, and the fractionation of soluble polymers into arabinoxylan- and (1-3,1-4)-β-d-glucan-rich fractions for subsequent analysis. This methodology is applied to endosperm flours from wheat, hull-less barley and rye, and could be extended to include studies on the effects of food processing with respect to yield and characteristics of the three fractions in order to better understand the structural basis for nutritional functionality

Comprehensive Molecular Characterization of Pheochromocytoma and Paraganglioma

We report a comprehensive molecular characterization of pheochromocytomas and paragangliomas (PCCs/PGLs), a rare tumor type. Multi-platform integration revealed that PCCs/PGLs are driven by diverse alterations affecting multiple genes and pathways. Pathogenic germline mutations occurred in eight PCC/PGL susceptibility genes. We identified CSDE1 as a somatically mutated driver gene, complementing four known drivers (HRAS, RET, EPAS1, and NF1). We also discovered fusion genes in PCCs/PGLs, involving MAML3, BRAF, NGFR, and NF1. Integrated analysis classified PCCs/PGLs into four molecularly defined groups: a kinase signaling subtype, a pseudohypoxia subtype, a Wnt-altered subtype, driven by MAML3 and CSDE1, and a cortical admixture subtype. Correlates of metastatic PCCs/PGLs included the MAML3 fusion gene. This integrated molecular characterization provides a comprehensive foundation for developing PCC/PGL precision medicine