QUANTITATIVE-DETERMINATION OF GLIADIN SUBGROUPS FROM DIFFERENT WHEAT CULTIVARS

Citation
H. Wieser et al., QUANTITATIVE-DETERMINATION OF GLIADIN SUBGROUPS FROM DIFFERENT WHEAT CULTIVARS, Journal of cereal science, 19(2), 1994, pp. 149-155
Citations number
14
Categorie Soggetti
Food Science & Tenology
Journal title
ISSN journal
07335210
Volume
19
Issue
2
Year of publication
1994
Pages
149 - 155
Database
ISI
SICI code
0733-5210(1994)19:2<149:QOGSFD>2.0.ZU;2-8
Abstract
Sixteen wheat cultivars originating from different countries and genot ypes and characterised by different technological properties were anal ysed for the amount and proportion of omega- and alpha-type and gamma- type gliadin subgroups. The optimal extraction of gliadin from flour w as achieved with 60% (v/v) aqueous ethanol after pre-extraction with a salt solution. The separation and quantitative determination was perf ormed by reversed-phase high-performance liquid chromatography on C-18 silica gel. The amount of both total gliadin and subgroups revealed d istinct inter-cultivar differences. Within the subgroups, the alpha-ty pe gliadins were generally present in greatest amount, followed by the gamma-type gliadins, whereas the omega-gliadins were present at lower levels. A strong statistical relationship was found between the prote in content of the flours and the amounts of total gliadin, alpha-type and gamma-type gliadins. Other flour properties (baking volume, SDS-se dimentation volume, dough resistance and extensibility) were correlate d only weakly with gliadin contents, with only omega 1,2-gliadins and gamma(A)- gliadins showing moderate negative and positive effects, res pectively. The proportions of omega- and alpha-type and gamma-type gli adins found within the total gliadin fraction covered broad ranges (al pha: 43.9-59.9%, gamma: 30.5-45.6%, omega: 6.2-20.0%). The proportions of the gliadin subgroups were to some extent related to the genotype of the cultivar. Thus, high proportions of omega-gliadins (17-20%) wer e typical for wheat/rye hybrids. In view of the inter-cultivar variati on observed, the value of immunochemical assays developed for the anal ysis of total gliadin in food is restricted if the reactivity of the a ntibodies used is not directed to all types of gliadin components but to the minor subgroups of omega-gliadins.