Abstract

Although the economic value of wheat flour is determined by the complement of gluten proteins, these proteins have been challenging to study because of the complexity of the major protein groups and the tremendous sequence diversity among wheat cultivars. The completion of a high-quality wheat genome sequence from the reference wheat Chinese Spring recently facilitated the assembly and annotation of a complete set of gluten protein genes from a single cultivar, making it possible to link individual proteins in the flour to specific gene sequences. In a proteomic analysis of total wheat flour protein from Chinese Spring using quantitative two-dimensional gel electrophoresis combined with tandem mass spectrometry, gliadins or low-molecular-weight glutenin subunits were identified as the predominant proteins in 72 protein spots. Individual spots were associated with 40 of 56 Chinese Spring gene sequences, including 16 of 26 alpha gliadins, 10 of 11 gamma gliadins, six of seven omega gliadins, one of two delta gliadins, and nine of ten LMW-GS. Most genes that were not associated with protein spots were either expressed at low levels in endosperm or encoded proteins with high similarity to other proteins. A wide range of protein accumulation levels were observed and discrepancies between transcript levels and protein levels were noted. This work together with similar studies using other commercial cultivars should provide new insight into the molecular basis of wheat flour quality and allergenic potential.

Highlights

  • Gluten proteins comprise about 70% of the total protein in wheat flour and are largely responsible for the functional properties that make it possible to produce a wide range of different food products from flour

  • The glutenins consist of high-molecular-weight glutenin subunits (HMW-GS) and low-molecular-weight glutenin subunits (LMW-GS) that are linked via intermolecular disulfide bonds to form large polymers that are essential for flour end-use quality

  • Based on the sizes of proteins deduced from the full-length gene sequences, Chinese Spring flour would be expected to contain 26 alpha gliadins that range from 30.0 to 36.2 kDa and have pIs from 6.18 to 8.28

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Summary

Introduction

Gluten proteins comprise about 70% of the total protein in wheat flour and are largely responsible for the functional properties that make it possible to produce a wide range of different food products from flour. Despite many years of study, the large numbers and closely related repetitive structures of these proline- and glutamine-rich proteins coupled with their sequence diversity in different cultivars have made it challenging to relate specific proteins to flour end-use quality. The gliadins are divided into four complex groups, termed alpha, gamma, delta, and omega gliadins, each containing numerous members with similar structures and. Most omega gliadins consist entirely of repetitive sequences and do not contain any cysteine. The glutenins consist of high-molecular-weight glutenin subunits (HMW-GS) and low-molecular-weight glutenin subunits (LMW-GS) that are linked via intermolecular disulfide bonds to form large polymers that are essential for flour end-use quality. A number of proteins with sequences similar to alpha, gamma, and omega gliadins contain an odd number of cysteine residues and are linked into the glutenin polymer. It has been hypothesized that these proteins, referred to as chain terminators, limit the size of the glutenin polymer and have a negative effect on end-use quality (Tao and Kasarda 1989)

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