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DOI: 10.1094/CC-82-0594
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ARTICLE
Flour Protein Composition and Functional Properties of Transgenic Rye Lines
Expressing HMW Subunit Genes of Wheat.
Herbert Wieser (1,2), Werner
Seilmeier (1), Rolf Kieffer (1), and Fredy Altpeter (3). (1) Deutsche
Forschungsanstalt für Lebensmittelchemie, Lichtenbergstr. 4, D-85748 Garching,
Germany. (2) Corresponding author. E-mail: <h.wieser@lrz.tum.de> (3) University of
Florida – IFAS, Agronomy Department, PMCB, Genetics Institute, 2191 Mc Carty
Hall, Laboratory of Molecular Plant Physiology, Gainesville FL 326611-0300.
Cereal Chem. 82(5):594-600. Accepted May 13, 2005. Copyright 2005 AACC
International, Inc.
Flours from nonsprouted (ns) kernels and dried sprouted (s) kernels of
transgenic rye expressing HMW glutenin subunits (HMW-GS) 1Dy10 (L10) or
1Dx5+1Dy10 (L5+10) from wheat were compared with flours from the corresponding
wildtype rye (Lwt). The crude protein content of nonsprouted flours ranged from
9.2% (Lwt) to 10.4% (L5+10) and was lowered by approximately 1% due to sprouting. Flour
proteins were separated into albumins/globulins, prolamins, and glutelin
subunits by a modified Osborne fractionation and into SDS-soluble and insoluble
fractions. Portions of the prolamin fractions were reduced in the same manner as
glutelins. The different fractions were then characterized and quantified by
RP-HPLC on C(8) silica gel. The proportion of albumins/globulins did not
significantly differ between transgenic lines and wildtype. The proportions of
alcohol-insoluble glutelins and SDS-insoluble proteins drastically increased in
transgenic rye due to a shift of HMW and gamma-75k secalins into the polymeric
fractions. Significant differences in the proportion of highly polymeric
proteins between nonsprouted and sprouted flours could not be detected. The
quantitative data demonstrated that the expression of HMW-GS led to a higher
degree of polymerization of storage proteins in rye flour. The HMW-GS
combination 1Dx5+1Dy10 showed stronger effects than 1Dy10 alone. The analyzed
flours contained two HMW secalins (R1, R2), whose amino acid compositions were
closely related to those of 1Dy10 and 1Dx5, respectively. The amounts of R1 in
Lwt flours determined by RP-HPLC were 221 mg (ns) and 186 mg (s) per 100 g and
those of R2 were 344 mg (ns) and 298 mg (s), respectively. These amounts
increased to 240 mg (ns)/201 mg (s) (R1) and 479 mg (ns)/432 mg (s) (R2) in L10
flours. In L5+10 flours, the amount of R1 decreased to 150 mg (ns)/132 mg (s)
while R2 increased to 432 mg (ns)/338 mg (s). The amount of HMW-GS 1Dy10 was
almost the same as that of R2 in L10 flours but was strongly increased in L5+10
flour (633 mg [ns]/538 mg [s]). HMW-GS 1Dx5 was, by far, the major subunit in
L5+10 flours (987 mg [ns]/896 mg [s]). The summarized amounts of all HMW
subunits increased from approximately 0.5 g (Lwt) to approximately 1.1 g (L10) and
approximately 2.0 g (L5+10). Thus
only L10 flours were similar to wheat flours in HMW subunit content. The baking
performance of L10 flour determined by a microbaking test was improved compared
with Lwt flour, whereas L5x10 flour showed very poor properties obviously due to
the strongly increased proportion of highly cross-linked glutelins. The
breadmaking quality of flours from 1Dy10 seeds and wildtype seeds was reduced by
the same degree when flours from sprouted seeds were analyzed.
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