Over-expression of HMW glutenin subunit Glu-B1 7x in hexaploid wheat varieties (Triticum aestivum)
M-J. Vawser A C and G. B. Cornish BA CRC for Molecular Plant Breeding, Urrbrae, SA 5064, Australia.
B South Australian Research and Development Institute, Grain Quality Research Laboratory, Urrbrae, SA 5064, Australia.
C Corresponding author: University of Adelaide, Waite Agricultural Research Institute, Discipline of Plant and Pest Science, Urrbrae, SA 5064, Australia.
Australian Journal of Agricultural Research 55(5) 577-588 https://doi.org/10.1071/AR03227
Submitted: 31 October 2003 Accepted: 23 February 2004 Published: 8 June 2004
Abstract
In Canada in 1993, a special market class of wheat, Canada Western Extra Strong (CWES), was established to segregate wheat varieties known to produce very strong and extensible doughs. These exceptional dough properties enable CWES cultivars to be blended with wheats of lesser quality as well as being suited to the manufacture of frozen dough products. The high molecular weight (HMW) glutenin allele (Glu-B1al) that confers these properties, particularly dough strength, has now been identified. Typically, the presence of the Glu-B1al (7+8*) allele is associated with the overexpression of HMW-GS 1Bx 7. RP-HPLC was used to quantify the proportion (% area) of individual HMW-GS relative to total HMW-GS in wheat varieties of different origin. The B genome contributed the highest percentage of HMW-GS, with the exception of Glu-B1d (6+8*) where the D genome contributed the most. Cultivars that possessed the Glu-B1al allele contained a significantly higher (P < 0.001) proportion of HMW-GS (56.80 ± 3.25%) encoded by the B genome. This suggests that the proportion of Glu-B1 subunits, relative to the total amount of HMW-GS expressed, has a major effect on dough strength. We also identified germplasm, of different origin, that contains the Glu-B1al allele and overexpresses subunit 7, including the most likely source of this allele in bread wheat cultivars. The Glu-B1al allele in the varieties identified in this paper could be traced, at least through one parent, to the Argentinean bread wheat cultivar Klein Universal II. RP-HPLC elution and expression profiles of various common HMW-GS are also discussed.
Additional keywords: quality, dough, protein, SDS-PAGE, RP_HPLC, Glu-1 allele, HMW-GS, Glu-B1al.
Acknowledgments
This work was funded by the CRC for Molecular Plant Breeding. The authors wish to thank Ms RE Tonkin, Grain Quality Research Laboratory, SARDI, for her assistance with the SDS–PAGE analysis of HMW-GS. Rheological data presented in Fig. 1 was kindly provided by Australian Grain Technologies (AGT).
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