Growth Environment Influences Grain Protein Composition and Dough Functional Properties in Three Australian Wheat Cultivars

The objectives of this study were to assess how functional properties of proteins in whole meal wheat (Triticum aestivum L.) flour vary across different growth environments. Grain from three commercial Australian Hard milling wheat cultivars was analyzed from four growth locations in 2008 and from two of the corresponding cultivars and locations in 2009. The protein content of the grain, soluble and insoluble extractable protein fractions, swelling index of glutenin (SIG), glutenin‐to‐gliadin ratio (Glu:Gli), percent unextractable polymeric protein (%UPP), and dough properties including force at maximum resistance (Rmax) and extensibility were measured. Based on analysis of variance of aggregated data for the cultivars, growth locations, and seasons, growth environment factors made significant contributions to variability in the total grain protein, Glu:Gli ratio, %UPP, SIG, Rmax, and extensibility of the wheat flour. Variability of protein content of the soluble and insoluble extractable protein fractions was mostly owing to genotype.     

Rapid Methods to Predict Soft-Wheat Dough Quality for Specific Food Products

A flour miller must provide flour with the potential to produce dough properties suited to the specifications for food manufacturers involved with a range of food products. This difficult task could be simplified if grain of suitable dough-forming potential was segregated at harvest and delivered for milling. To achieve the identification of grain of suitable dough-quality potential, various published testing systems were adapted and evaluated using a total of 149 grain samples from five successive harvests to establish procedures that could be applied to “running samples”, each representing the contents of a specific storage cell. Some of the methods proved to be inadequate for this purpose. The best possibilities were methods based on the swelling index for glutenin (SIG) principle. The SIG test, combined with grain-protein content, is suitable for screening large numbers of wheat meal samples, making it possible for mill buyers to select stored grain lots that will suit the flour dough strength specifications for specific customers and their food products.     

Rheological properties of wheat flour processed at low levels of hydration: Influence of starch and gluten

The rheological properties of wheat flour under processing such as extrusion (with 28% moisture content, wet basis) are influenced by the molecular changes its components undergo during processing. But, there was no simple relationship between the wheat-flour characteristics and their rheological properties. In order to investigate the quantitative and qualitative effects of the individual flour components on rheological properties, model blends of wheat starch and wheat gluten with different starch/gluten ratios were studied. The effects of gluten and starch quality were also investigated by using different gluten types and by modifying the amylose content of starch, respectively. The shear viscosity of the blends, determined by capillary rheometry under controlled conditions (35% moisture content, 140 °C), was observed to be modified by both gluten and amylose content. The changes undergone by wheat gluten under these conditions were analysed by HPLC, to determine the levels of unextractable polymeric proteins, and by Lab-on-a-Chip analysis of protein composition, to follow the polymerisation of protein under processing. This study indicated that in low hydrated products in the molten state, shear viscosity is affected by the structure of the blends as determined by fluorescence microscopy and by the molecular changes occurring during processing.     

Influence of storage conditions on the structure, thermal behavior, and formation of enzyme-resistant starch in extruded starches

Starch structures from an extrusion process were stored at different temperatures to allow for molecular rearrangement (retrogradation); their thermal characteristics (DSC) and resistance to amylase digestion were measured and compared. The structure of four native and processed starches containing different amylose/amylopectin compositions (3.5, 30.8, 32, and 80% amylose content, respectively) before and after digestion was studied with small-angle X-ray scattering (SAXS) and X-ray diffraction (XRD). Rearrangement of the amylose molecules was observed for each storage condition as measured by the DSC endotherm at around 145 degrees C. The crystalline organization of the starches after processing and storage was qualitatively different to that of the native starches. However, there was no direct correlation between the initial crystallinity and the amount of enzyme-resistant starch (ERS) measured after in vitro digestion, and only in the case of high-amylose starch did the postprocess conditioning used lead to a small increase in the amount of starch remaining after the enzymatic treatment. From the results obtained, it can be concluded that retrograded amylose is not directly correlated with ERS and alternative mechanisms must be responsible for ERS formation.     

On-the-spot identification of grain variety and wheat-quality type by Lab-on-a-chip capillary electrophoresis

Lab-on-a-chip capillary electrophoresis has been used for identification of wheat variety and quality type. Analysis of each chip takes 30 minutes for 10 samples, and distinction can be made between members of a set of 40 commonly grown Australian wheat varieties. Quality type could be predicted by analysis of the HMW and LMW glutenin subunits. The technique has also been applied to the separation of proteins from other grains and legumes, and may also be useful for identifying variety and/or quality type in these crops.     

Synergistic and Additive Effects of Three High Molecular Weight Glutenin Subunit Loci. II. Effects on Wheat Dough Functionality and End‐Use Quality

Understanding the relationship between basic and applied rheological parameters and the contribution of wheat flour protein content and composition in defining these parameters requires information on the roles of individual flour protein components. The high molecular weight glutenin subunit (HMW‐GS) proteins are major contributors to dough strength and stability. This study focused on eight homozygous wheat lines derived from the bread wheat cvs. Olympic and Gabo with systematic deletions at each of three HMW‐GS encoding gene loci, Glu‐A1, Glu‐B1, and Glu‐D1. Flour protein levels were adjusted to a constant 9% by adding starch. Functionality of the flours was characterized by small‐scale methods (2‐g mixograph, microextension tester). End‐use quality was evaluated by 2‐g microbaking and 10‐g noodle‐making procedures. In this sample set, the Glu‐D1 HMW‐GS (5+10) made a significantly larger contribution to dough properties than HMW‐GS coded by Glu‐B1 (17+18), while subunit 1 coded by Glu‐A1 made the smallest contribution to functionality. These differences remained after removing variations in glutenin‐to‐gliadin ratio. Correlations showed that both basic rheological characteristics and protein size distributions of these flours were good predictors of several applied rheological and end‐use quality tests.     

Incorporation of soy proteins into the wheat–gluten matrix during dough mixing

Farinograph methodology was used to evaluate the possible incorporation of soy proteins into a glutenin–soy complex during mixing and to study the contribution of soy proteins to the chemical and physical properties of the dough. To facilitate the interaction of soy and wheat proteins, a redox process was used, which allowed the partial reduction (using dithiothreitol, DTT) and subsequent reoxidation (using potassium iodate) of glutenin without changing its functionality in the dough (a composite of equal parts of wheat and soy flours, 300 g in total). Either raw soy flour (RSF) or physically modified soy flour (PMSF) was used as the soy component. Dough samples were taken at peak mixing time and at break time during mixing, and these were freeze dried for SE-HPLC analysis and capillary electrophoresis (Lab-on-a-chip).     

A suspension model of the linear viscoelasticity of gluten doughs

We regard gluten dough as a mixture of gluten, starch and water. We show that stress intensification around the starch particles enables one to describe the rapid strain softening of dough at low strains. The starch is in the form of a combination of A-particles (close to oblate spheroids) and B-particles (almost spherical). This suggests that a suspension theory should be able to account for the linear viscoelastic properties of doughs. We develop a new representation for the prediction of the linear viscoelastic properties of a viscoelastic matrix (gluten) with embedded oblate spheroids and spherical particles. The calculations are compared with experiments on gluten mixes derived from an Australian Baker’s flour. We note that the non-sphericity of the A-particles is very important in stiffening the gluten matrix and also that the effective volume fraction of the starch is greater than that calculated by assuming a starch density of 1.4 g/ml.     

Rapid DNA-based identification of wheat and barley varieties

Micro-fluidic capillary electrophoresis methodology was developed to analyse grain DNA composition, thus to provide unequivocal distinction between varieties of wheat (Triticum aestivum L.) and of barley (Hordeum vulgare L.). This ‘Lab-on-a-chip’ technology complements protein composition analysis by micro-fluidic capillary electrophoresis, which is already in routine use for variety identification. Whereas it had been difficult to distinguish between some varieties by protein analysis using the Lab-on-a-chip system, distinctions proved to be possible using a combination of DNA extraction and microsatellite analysis, taking advantage of the speed and convenience of DNA chips. Several combinations of microsatellites permitted the DNA analysis system to provide distinction between two wheat varieties and between all but two (Chebec and Schooner) of the main eleven Australian barley varieties (Arapiles, Baudin, Barque, Chebec, Gairdner, Grimmett, Lindwall, Parwan, Schooner, Skiff and Sloop).     

Synergistic and Additive Effects of Three High Molecular Weight Glutenin Subunit Loci. I. Effects on Wheat Dough Rheology

The high molecular weight glutenin subunits (HMW‐GS) play an important role in governing the functional properties of wheat dough. To understand the role of HMW‐GS in defining the basic and applied rheological parameters and end‐use quality of wheat dough, it is essential to conduct a systematic study where the effect of different HMW‐GS are determined. This study focuses on the effect of HMW‐GS on basic rheological properties. Eight wheat lines derived from cvs. Olympic and Gabo were used in this study. One line contained HMW‐GS coded by all three loci, three lines were each null at one of the loci, three lines were null at two of the loci and one line null at all three loci. The flour protein level of all samples was adjusted to a constant 9% by adding starch. In another set of experiments, in addition to the flour protein content being held at 9%, the glutenin‐to‐gliadin ratio was maintained at 0.62 by adding gliadin. Rheological properties such as elongational, dynamic, and shear viscometric properties were determined. The presence of Glu‐D1 subunits (5+10) made a significantly larger contribution to dough properties than those encoded by Glu‐B1 (17+18), while subunit 1, encoded by Glu‐A1, made the least contribution to functionality. Results also confirmed that HMW‐GS contributed to strength and stability of dough.