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BT型杂交粳稻育性及其三系的若干蛋白质标记(英文) 被引量:8
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作者 洪德林 佐藤光 +2 位作者 熊丸敏博 曲乐庆 U S SADAR 《中国水稻科学》 CAS CSCD 北大核心 2001年第3期165-168,共4页
用十二烷基硫酸钠聚丙烯酰胺凝胶电泳 (SDS- PAGE)方法 ,对粳稻 BT细胞质雄性不育系六千辛 A,保持系六千辛 B,恢复系六千辛 R、7730 2 - 1,以及杂交组合六千辛 A/7730 2 - 1的 F1 和 F2 种子的胚乳贮藏蛋白进行了分析。结果表明 ,在谷... 用十二烷基硫酸钠聚丙烯酰胺凝胶电泳 (SDS- PAGE)方法 ,对粳稻 BT细胞质雄性不育系六千辛 A,保持系六千辛 B,恢复系六千辛 R、7730 2 - 1,以及杂交组合六千辛 A/7730 2 - 1的 F1 和 F2 种子的胚乳贮藏蛋白进行了分析。结果表明 ,在谷蛋白α- 3区域 ,恢复系有两条带α- 3a和α- 3b,而六千辛 A和六千辛 B只有一条带α- 3。 F2 代具有α- 3的种子和具有α- 3a加α-3b的种子 1∶ 1分离。谷蛋白α- 4带的移动速率 ,恢复系比六千辛 A快。把较快的α- 4带记为α- 4f。 F2 代具有α- 4的种子和具有 α- 4加 α- 4f的种子也是 1∶ 1分离 ,与配子体不育类型的 F2 代花粉育性恢复基因分离比一致。系谱分析表明六千辛 R中 α-3a和α- 3b来源于 IR8。六千辛 A比六千辛 展开更多
关键词 粳稻 恢复系 细胞质雄性不育性 蛋白质标记 杂交水稻 谷蛋白 醇溶蛋白
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水稻种子储藏蛋白及其基因表达 被引量:12
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作者 陈豫 曲乐庆 贾旭 《遗传》 CAS CSCD 北大核心 2003年第3期367-372,共6页
作为人类氮素营养的一个重要来源,水稻种子储藏蛋白的组成、结构及其合成过程一直是为研究者所关注。随着研究的深入,对于谷蛋白基因的结构特点,表达方式以及与谷蛋白基因表达相关的转录因子也都为人们所逐渐了解。这些知识对于人们改... 作为人类氮素营养的一个重要来源,水稻种子储藏蛋白的组成、结构及其合成过程一直是为研究者所关注。随着研究的深入,对于谷蛋白基因的结构特点,表达方式以及与谷蛋白基因表达相关的转录因子也都为人们所逐渐了解。这些知识对于人们改善水稻籽粒的品质以及利用水稻籽粒来生产外源蛋白都具有十分重要的意义。本文对这些方面做一简要概述。 展开更多
关键词 水稻 种子 储藏蛋白 基因表达 籽粒 品质 外源蛋白
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水稻转基因研究及新品种选育 被引量:13
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作者 朱祯 曲乐庆 张磊 《生物产业技术》 2010年第3期27-34,共8页
水稻是最重要的粮食作物之一,世界上约有一半以上的人口以稻米为主食。我国水稻每年播种面积在4.2亿~4.5亿亩(1亩=0.067公顷.下同)之间,占粮食总产量的38%、食粮的70%,在粮食生产中占有举足轻重的地位。随着人口的增长和耕... 水稻是最重要的粮食作物之一,世界上约有一半以上的人口以稻米为主食。我国水稻每年播种面积在4.2亿~4.5亿亩(1亩=0.067公顷.下同)之间,占粮食总产量的38%、食粮的70%,在粮食生产中占有举足轻重的地位。随着人口的增长和耕地面积的减少.我国将面临粮食问题的严峻挑战。FAO(联合国粮农组织)认为.今后国际粮食总产增长的80%将依赖于单产水平的提高,而单产提高的60%~80%来源于良种的科技进步。传统的育种技术已为培育水稻新品种做出了巨大贡献, 展开更多
关键词 水稻新品种 转基因技术 新品种选育 联合国粮农组织 粮食总产量 应用 粮食作物 单产水平
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认识和改良中国小麦蛋白质量的遗传基础:策略与现有的研究
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作者 王道文 曲乐庆 +3 位作者 贾旭 张相岐 万永芳 李振声 《遗传》 CAS CSCD 北大核心 2001年第1期45-45,共1页
Seed protein content, nutritional balance and processing property of flour are the three major aspects of wheat protein quality. Most Chinese wheat cultivars are comparable to their Western counterparts in terms of se... Seed protein content, nutritional balance and processing property of flour are the three major aspects of wheat protein quality. Most Chinese wheat cultivars are comparable to their Western counterparts in terms of seed protein content and nutritional balance. However, relatively few of them possess good processing property. The main reason underlying the poor processing property of hexaploid Chinese wheat varieties is the weakness in gluten strength. Considering that wheat gluten is mainly composed of a mixture of a finite number of storage protein species and that the storage protein species may determine gluten strength through combinatorial controls, we formed the following strategies in our studies on understanding and manipulating the genetic basis of protein quality in Chinese wheat. 1. Genetic analysis. By performing well structured genetic analysis, we hope to identify two types of storage protein genes, those genes whose presence is associated with good processing property (the desirable genes, or the D type genes) and those whose presence is always associated with undesirable processing property (the undesirable genes, or the U type genes). Two sets of genetic analysis are being conducted currently. The aim of the first set of analysis is to obtain nonfunctional mutants for the majority of the genes whose products are present in the gluten. This analysis is expected to yield information on the function of individual members of storage proteins, some of which may be encoded by the D type genes, in gluten strength control. The aim of the second set of analysis is to identify potential genetic factors that may be responsible for causing weakness in gluten strength in Chinese wheat through the use of recombinant inbreed lines. This analysis may produce information on the function of the storage proteins specified by the U type genes. 2. Molecular analysis. On the basis of above genetic analysis, a molecular approach will be undertaken to clone the D and U type genes. The cloned genes will be characterized in terms of genetic diversity in cultivated wheat and wild species related to wheat and potential application in molecular breeding for processing property improvement. Because of the known association between the HMW glutenin subunit 1D×5 and good processing quality, we are now searching wheat related wild species for better versions of the 1D×5 subunit and testing their potential in wheat processing quality improvement. 3. Molecular breeding. The above genetic and molecular analysis should result in sufficient gene and marker resources suitable for wheat processing quality improvement through molecular breeding. The D type genes will be transferred into high yielding, hexaploid wheat varieties using the transgenic technology. The molecular markers linked to the U type of genes will be used to screen breeding materials for an early avoidance of this type of genes in breeding programs. In summary, the combination of theoretical and applied investigations described above should contribute to wheat protein quality improvement in both China and abroad. In the future, wheat quality breeding will be a more productive and efficient enterprise worldwide. 展开更多
关键词 小麦 蛋白质 遗传基因 改良
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