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Thermal and Pasting Properties, Morphology of Starch Granules, and Crystallinity of Endosperm Starch in the Rice SSI and SSIIIa Double-Mutant

机译:水稻SSI和SSIIIa双突变体的热糊化特性,淀粉颗粒的形态和胚乳淀粉的结晶度

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摘要

Starch is glucose polymer linked by α-1,4 and α-1,6 glucosidic bonds. The balance of activity between starch synthases (SSs) and branching enzymes (BEs) is important for formation of amylopectin structure. SSI and SSIIIa isozymes account for 60 and 30%, respectively, of soluble SS activity in developing rice endosperm. Complete loss of both SSI and SSIIIa activities induces sterility. By contrast, a double mutant (ss1~L/ss3a) generated by crossing the leaky ss1 mutant, whose SS activity is approximately ca. 16% of the wild type, and the ss3a null mutant is fertile. Although there is only a significant residual SS activity in the developing endosperm of ss1~L/ss3a, the yield and growth of the double-mutant line is sufficient. We analyzed the amylopectin chain-length distribution, thermal and pasting properties, morphologies of starch granules and amyloplasts, and crystallinity of endosperm starch in ss1~L/ss3a and the parental mutant lines. The chain-length distribution pattern of ss1~L/ss3a was similar to that of ss3a and there was an additive effect of the reduction of SSI activity on the chain-length of amylopectin in the ss3a background. These changes in the amylopectin chain-length distribution were considered to increase the gelatinization temperature of the starch. The gelatinized starch viscosity of the double-mutant and ss3a lines was very low. Most ss1~L/ss3a starch granules were round-shaped, and the starch granular size was smaller than those of the parental mutant lines and the wild type. The starch crystallinity of ss1~L/ss3a was slightly reduced compared with that of the wild type.
机译:淀粉是通过α-1,4和α-1,6糖苷键连接的葡萄糖聚合物。淀粉合酶(SSs)和分支酶(BEs)之间的活性平衡对于支链淀粉结构的形成很重要。在发育的水稻胚乳中,SSI和SSIIIa同工酶分别占可溶性SS活性的60%和30%。 SSI和SSIIIa活性完全丧失会导致不育。相比之下,双重突变体(ss1〜L / ss3a)是通过与渗漏的ss1突变体杂交而产生的,其SS活性约为ca。 16%的野生型和ss3a无效突变体可育。尽管在发育中的ss1〜L / ss3a胚乳中仅存在明显的残留SS活性,但双突变株的产量和生长是足够的。我们分析了支链淀粉的链长分布,热和糊化特性,淀粉颗粒和淀粉质体的形态以及胚乳淀粉在ss1〜L / ss3a和亲本突变系中的结晶度。 ss1〜L / ss3a的链长分布模式与ss3a相似,并且在ss3a背景下,SSI活性降低对支链淀粉的链长有累加效应。支链淀粉链长分布的这些变化被认为增加了淀粉的糊化温度。双突变体和ss3a系的糊化淀粉粘度非常低。多数ss1〜L / ss3a淀粉颗粒为圆形,且淀粉颗粒尺寸小于亲本突变系和野生型。与野生型相比,ss1〜L / ss3a的淀粉结晶度略有降低。

著录项

  • 来源
    《Journal of Applied Glycoscience》 |2015年第2期|81-86|共6页
  • 作者单位

    Laboratory of Plant Physiology, Department of Biological Production, Faculty of Bioresource Sciences, Akita Prefectural University (241-438 Kaidobata-nishi, Shimoshinjo-nakano, Akita 010-0195, Japan);

    Laboratory of Plant Physiology, Department of Biological Production, Faculty of Bioresource Sciences, Akita Prefectural University (241-438 Kaidobata-nishi, Shimoshinjo-nakano, Akita 010-0195, Japan);

    Laboratory of Plant Physiology, Department of Biological Production, Faculty of Bioresource Sciences, Akita Prefectural University (241-438 Kaidobata-nishi, Shimoshinjo-nakano, Akita 010-0195, Japan);

    Laboratory of Plant Physiology, Department of Biological Production, Faculty of Bioresource Sciences, Akita Prefectural University (241-438 Kaidobata-nishi, Shimoshinjo-nakano, Akita 010-0195, Japan);

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  • 正文语种 eng
  • 中图分类
  • 关键词

    differential screening calorimetry (DSC); scanning electron microscopy (SEM); starch synthase; rapid visco analyzer (RVA); X-ray diffraction;

    机译:差示筛选量热法(DSC);扫描电子显微镜(SEM);淀粉合酶快速粘度分析仪(RVA);X射线衍射;

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