首页> 外文学位 >GENETIC ANALYSIS OF THE HOR-3 LOCUS AND CHARACTERIZATION OF ITS PRODUCTS IN BARLEY (HORDEUM VULGARE, L.).
【24h】

GENETIC ANALYSIS OF THE HOR-3 LOCUS AND CHARACTERIZATION OF ITS PRODUCTS IN BARLEY (HORDEUM VULGARE, L.).

机译:大麦(HORDEUM VULGARE,L.)HOR-3基因座的遗传分析及其产物表征。

获取原文
获取原文并翻译 | 示例

摘要

The genes encoding the major storage proteins (hordeins) of barley have been previously designated the Hor loci. Two Hor loci, Hor-1 and Hor-2, have been mapped to the short arm of barley chromosome 5, approximately 10-15 centimorgans apart. A third Hor locus, Hor-3 is described and has been determined to lie approximately 30 centimorgans toward the centromere from the Hor-1 locus by recombination analysis.;The near 100,000 molecular weight glutelins of wheat have been implicated in bread wheat baking quality. While there may be significant differences between D hordein of barley and these wheat proteins, no obviously important differences were discovered by this study which could explain the lack of dough strength in barley.;A method for the purification of microgram quantities of D hordein is described. The stability of D hordein to extensive reduction is assessed and the amino acid composition of D hordein from the barley varieties 'Advance', 'Bomi' and 'Hiproly' determined. A glutelin of wheat with similar molecular weight and pI was purified from the variety 'Peak 72'. These four proteins were then subjected to peptide mapping using cyanogen bromide, DPCC-trypsin, chymotrypsin and Staphylococcus aureus V8 protease. Cyanogen bromide failed to cleave within the proteins, while trypsin and chymotrypsin cleaved the proteins into fragments too small to effectively resolve by sodium dodecyl sulfate polyacrylamide gel electrophoresis. Staphylococcus aureus V8 protease cleaved the proteins into a few fragments ranging in apparent molecular weights from 15,000 to 30,000. The conservation of cleavage sites within the proteins indicates the extreme similarity of these proteins.
机译:大麦的主要存储蛋白(大麦醇溶蛋白)的编码基因以前被称为Hor基因座。已将两个Hor基因座Hor-1和Hor-2定位到大麦5号染色体的短臂,相距约10-15厘摩。描述了第三个Hor基因座Hor-3,并通过重组分析确定它位于距Hor-1基因座向着着丝粒约30厘摩的位置。面包小麦的烘烤品质与近100,000分子量的小麦谷蛋白有关。虽然大麦的大麦醇溶蛋白与这些小麦蛋白之间可能存在显着差异,但本研究未发现明显的重要差异,这可以解释大麦的面团强度不足。 。评估了大麦醇溶蛋白对大量还原的稳定性,并确定了来自大麦品种“ Advance”,“ Bomi”和“ Hiproly”的大麦醇溶蛋白的氨基酸组成。从“ Peak 72”品种中纯化出具有相似分子量和pI的小麦谷蛋白。然后使用溴化氰,DPCC-胰蛋白酶,胰凝乳蛋白酶和金黄色葡萄球菌V8蛋白酶对这四种蛋白质进行肽图分析。溴化氰无法在蛋白质中裂解,而胰蛋白酶和胰凝乳蛋白酶则将蛋白质裂解成很小的片段,无法通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳有效地分离。金黄色葡萄球菌V8蛋白酶将蛋白质切割成几个片段,其表观分子量为15,000至30,000。蛋白质内切割位点的保守性表明这些蛋白质的极端相似性。

著录项

  • 作者

    BLAKE, THOMAS KEITH.;

  • 作者单位

    Washington State University.;

  • 授予单位 Washington State University.;
  • 学科 Biology Genetics.
  • 学位 Ph.D.
  • 年度 1983
  • 页码 89 p.
  • 总页数 89
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号