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Review: Amylopectin synthesis and hydrolysis – understanding isoamylase and limit dextrinase and their impact on starch structure on barley (Hordeum vulgare) quality

机译:综述:支链淀粉的合成和水解–了解异淀粉酶和极限糊精酶及其对淀粉结构对大麦(Hordeum vulgare)品质的影响

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摘要

Background Starch contributes to barley grain and malt quality which in turn contributes to beer quality and flavour; through fermentable sugar profiles, rates of fermentation and Mallard reactions. Both amylopectin and amylose are enzymatically degraded to release maltose, maltotriose and higher order sugars. Scope and approach Amylopectin is highly branched [α-(1 → 6) glycoside bond branch points] with numerous short branches while amylose is a long chained polymer with a few side branches. During grain development, the final level of branching is controlled by two enzymes namely; isoamylase and limit dextrinase (LD). Mutations in either of these genes can also result in changes to structure, content, and granule formation and size. During the malting free LD will to cleave the α-(1 → 6) bonds but during mashing processes, bound LD is release, resulting in chains of various length available for other starch degrading enzymes to hydrolyse. Findings and conclusions While there is a good understanding of most of the individual aspects in amylopectin formation, structure and degradation; the story remains incomplete, as most of this understanding has been gained from experiments with only a limited number of barley varieties, limitations in the technology for structural measurement, and since no data is available to link structure to fermentable sugar profiles.
机译:背景淀粉有助于改善大麦籽粒和麦芽的品质,进而有助于改善啤酒的品质和风味。通过可发酵的糖分布,发酵速率和野鸭反应。支链淀粉和直链淀粉均被酶降解以释放出麦芽糖,麦芽三糖和更高阶的糖。范围和方法支链淀粉是高度分支的[α-(1→6)糖苷键分支点],具有许多短分支,而直链淀粉是具有一些侧分支的长链聚合物。在谷物发育过程中,最终的分支水平受两种酶控制:异淀粉酶和极限糊精酶(LD)。这些基因之一的突变也可能导致结构,含量以及颗粒形成和大小的改变。在制麦过程中,游离的LD将裂解α-(1→6)键,但在糖化过程中,结合的LD被释放,导致各种长度的链可供其他淀粉降解酶水解。结论和结论尽管对支链淀粉的形成,结构和降解的大多数方面都有很好的了解,故事还不完整,因为大多数了解是通过仅使用有限数量的大麦品种的实验获得的,结构测量技术的局限性,并且由于没有可用的数据将结构与可发酵糖谱联系起来。

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    Gous, Peter W.; Fox, Glen P.;

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  • 年度 2017
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  • 原文格式 PDF
  • 正文语种 eng
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