Stefan Harasymow

Quantitative trait loci controlling kernel discoloration in barley (Hordeum vulgare L.)

Barley kernel discoloration (KD) leads to substantial annual loss in value through downgrading and discounting of malting barley. KD is a difficult trait to introgress into elite varieties as it is controlled by multiple genes and strongly influenced by environment and maturity. As the first step towards marker assisted selection for KD tolerance, we mapped quantitative trait loci (QTLs) controlling KD measured by grain brightness [Minolta L; (Min L)], redness (Min a), and yellowness (Min b) in 7 barley populations. One to 3 QTLs were detected for grain brightness in various populations, and one QTL could account for 5–31% of the phenotypic variation. The QTL located around the centromere region of chromosome 2H was consistently detected in 6 of the 7 populations, explaining up to 28% of the phenotypic variation. In addition, QTLs for grain brightness were most frequently identified on chromosomes 3H and 7H in various populations. Australian varieties Galleon, Chebec, and Sloop contribute an allele to increase grain brightness on chromosome 7H in 3 different populations. A major gene effect was detected for grain redness. One QTL on chromosome 4H explained 54% of the phenotypic variation in the Sloop/Halcyon population, and was associated with the blue aleurone trait. A second QTL was detected on the long arm of chromosome 2H in 3 populations, accounting for 23–47% of the phenotypic variation. The major QTLs for grain yellowness were mapped on chromosomes 2H and 5H. There were strong associations between the QTLs for heading date, grain brightness, and yellowness. The molecular markers linked with the major QTLs should be useful for marker assisted selection for KD.

Variation in grain β-glucan due to site, cultivar and nitrogen fertiliser in Western Australia

To adjust to projected changes in the future climate, maltsters are looking to reduce their water use. One option is to reduce the number of periods of water immersion during steeping from two to one. This might be possible if cultivars with very low grain β-glucan are used, as high β-glucan concentrations can restrict water penetration into the endosperm and the speed of germination. This study compared the grain β-glucan and various grain quality traits of nine two-row, Australian barley cultivars when grown at three sites with four rates of nitrogen (N) in Western Australia. Significant differences in grain β-glucan were found. Of the main factors, cultivar was found to have the largest effect on grain β-glucan followed by site, with N having the smallest effect. Grain β-glucan increased with increasing N application at two of the three sites. Not all cultivars responded similarly to N application. Grain with low β-glucan concentration generally had lower hectolitre weights, higher screenings, lower grain protein and was softer than grain with high grain β-glucan. There was no correlation between grain β-glucan and average grain weight, grain brightness or malt extract. The implication of these interactions and correlations in the breeding of very low grain β-glucan cultivars suited to single steep malting is discussed.

Molecular marker-assisted backcrossing breeding: an example to transfer a thermostable β-amylase gene from wild barley

Molecular marker-assisted backcrossing (MABC) is widely recommended for transferring favorable alleles from a donor to an elite variety. The question remains whether MABC is an effective approach to developing a competitive commercial variety. Here, we illustrate the transfer of a thermostable β-amylase allele Sd3 from wild barley into a commercial barley variety Gairdner. The elite lines were chosen for the Regional Crop Variety Test that followed a standard conventional breeding process. The results demonstrated that the Sd3 allele not only increased enzyme thermostability but dramatically enhanced diastatic power, an important malting quality trait. The BC1F1 individuals had a fundamental impact on the comprehensive agronomic and quality traits of the final progenies, demonstrating the importance of screening at the early stage of backcrossing in MABC. There was sufficient genetic variation in the BC3F3 families to select other malting quality and agronomic traits. Ten individual breeding lines with improved β-amylase thermostability also had improved yields and grain plumpness. Three elite lines with improved malting quality and agronomic traits were selected to provide a parental line to incorporate the wild barley allele for breeding a commercial variety. A new strategy should be considered that uses marker-assisted selection and backcrossing to transfer a favorable allele from a wild parent.