Mapping components of flour and noodle colour in Australian wheat
D. J. Mares and A. W. Campbell
Australian Journal of Agricultural Research 52(12) 1297 - 1309
Abstract
Flour and noodle colour influence the value of wheat
(Triticum aestivum L.) and are obvious targets for
breeders seeking to improve quality, end-product range, and marketability of
wheat. The objective of this investigation was to identify quantitative trait
loci (QTLs) associated with flour and noodle colour traits and with individual
components of colour. One hundred and sixty-three doubled haploid lines
derived from Sunco Tasman, white-grained, prime hard, and hard wheats adapted
to the north-eastern region of Australia were used for the bulk of this study
and were supplemented by doubled haploid populations derived from CD87 Katepwa
and Cranbrook Halberd for comparisons of flour colour. Samples of Sunco
Tasman, together with parental lines, were grown at Narrabri, NSW, in 1998 and
1999 and at Roma, Qld, in 1998 and used for visible light reflectance
measurements of flour brightness (CIE L*) and yellowness (CIE b*), and
white salted noodle (WSN) and yellow alkaline noodle (YAN) brightness,
yellowness, and colour stability. Xanthophyll content and polyphenol oxidase
(PPO) activity were measured spectrophotometrically.
No consistent QTLs were identified for flour L* or initial L* of WSN and YAN. Xanthophyll content was very strongly associated with QTLs located on chromosomes 3B and 7A and these QTLs also had a major influence on flour b*, WSN b*, and YAN b*. Noodle brightness at 2, 24, and 48 h and the magnitude of change in noodle L* and b* with time were affected by QTLs on 2D, contributed by Tasman, and, to a lesser degree, 2A. The QTL on 2D was clearly associated with control of grain PPO, an enzyme implicated in darkening of Asian style noodles. QTLs located on 2B, 4B, and 5B and associated with control of grain size or flour protein content also appeared to influence a number of colour traits.
Keywords: colour stability, xanthophyll, polyphenol oxidase.
Full text doi:10.1071/AR01048
© CSIRO 2001





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