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Assessment of Enzymatic Endosperm Modification of Malting Barley Using Individual Grain Analyses

机译:使用单个谷物分析评估发芽大麦的酶促胚乳修饰

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Enzymatic modification of the endosperm of malting barley is a main feature of the malting process. Uneven enzymatic modification of the endosperm (heterogeneity) can cause brewhouse problems. Although there is a general correlation between endosperm modification, beta-glucan breakdown and endo-beta-glucanase development, it is based on average results from sample analyses and may conceal heterogeneity. The primary aim of this work was to use individual grain analyses to investigate factors that control endosperm modification and beta-glucan breakdown. In terms of beta-glucan breakdown and physical modification, the barley variety Chariot malted faster than Decanter. However, both varieties showed similar distribution of endo-beta-glucanase in individual grains during malting. Further work on individual grains showed that the correlation between beta-glucan breakdown and endo-beta-glucanase activity was not significant. Surprisingly beta-glucan breakdown did not always correlate with the physical modification of the endosperm. Both these findings suggest that sample analyses of beta-glucan levels and malt beta-glucanase activities are not reliable indicators of the degrees of which malt samples are modified during malting. Since the distribution of beta-glucan in individual grains of the unmalted barley varieties was similar, the total beta-glucan levels of the original barley did not determine the rate at which beta-glucan was broken-down during malting. Although protein studies are at a preliminary stage, the rate of protein breakdown was not correlated with the rate at which beta-glucan was broken down in the malting grain. It is possible that the physico-chemical properties of endosperm storage proteins may limit the rate of beta-glucan breakdown during malting.
机译:麦芽大麦胚乳的酶促修饰是麦芽过程的主要特征。胚乳的酶促修饰不均匀(异质性)可能会导致啤酒厂出现问题。尽管胚乳修饰,β-葡聚糖降解和β-葡聚糖内切酶发育之间存在一般关联,但它基于样品分析的平均结果,可能掩盖了异质性。这项工作的主要目的是使用单独的谷物分析来研究控制胚乳修饰和β-葡聚糖分解的因素。就β-葡聚糖的分解和物理修饰而言,大麦品种Chariot的发芽速度快于Decanter。但是,这两种变种在制麦芽过程中均在单个谷物中显示出相似的内切β-葡聚糖酶分布。对单个谷物的进一步研究表明,β-葡聚糖分解与内切β-葡聚糖酶活性之间的相关性不显着。令人惊讶的是,β-葡聚糖的分解并不总是与胚乳的物理修饰相关。这些发现都表明,对β-葡聚糖水平和麦芽β-葡聚糖酶活性的样品分析不是麦芽制过程中麦芽样品被修饰程度的可靠指标。由于未经发芽的大麦品种的单个谷物中β-葡聚糖的分布相似,因此原始大麦的总β-葡聚糖含量无法确定制麦过程中β-葡聚糖的分解率。尽管蛋白质研究尚处于初步阶段,但蛋白质分解的速度与麦芽谷物中β-葡聚糖的分解速度无关。胚乳贮藏蛋白的物理化学性质可能会限制麦芽制程中β-葡聚糖的分解速率。

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