华北农学报 ›› 2004, Vol. 19 ›› Issue (4): 11-13. doi: 10.3321/j.issn:1000-7091.2004.04.004

所属专题: 棉花

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棉花晋A及其保持系酯酶过氧化物酶PAGE电泳分析

李成奇1, 石跃进1, 潘转霞1, 袁钧1, 刘巷禄1, 任雪峰2   

  1. 1. 山西省农业科学院棉花研究所, 山西 运城 044000;
    2. 运城市农业局, 山西 运城 044000
  • 收稿日期:2003-10-18 出版日期:2004-12-28
  • 作者简介:李成奇(1974-),男,山西临猗人,助理研究员,在读硕士,主要从事棉花遗传育种工作.
  • 基金资助:
    国家863项目(2001AA212021)

PAGE Analysis on Esterase and Peroxidase of "JinA-line and B-line" in Cotton

LI Cheng-qi1, SHI Yue-jin1, PAN Zhuan-xia1, YUAN Jun1, LIU Xiang-lu1, REN Xue-feng2   

  1. 1. Cotton Research Institute, Shanxi Academy of Agricultural Sciences, Yuncheng044000, China;
    2. Agricultural Bureau of Shanxi Yuncheng City, Yuncheng044000, China
  • Received:2003-10-18 Published:2004-12-28

摘要: 采用聚丙烯酰胺凝胶电泳(PAGE)方法,对晋A棉花质核雄性不育系及其保持系作了酯酶过氧化物酶同工酶分析。结果表明,晋A及其保持系两种同工酶在所有器官上均具有一些共同的基本酶带,在营养器官上无较大差别,说明它们具有基本一致的遗传背景。受育性基因的影响,进入生殖阶段,在造孢细胞增殖时期的花蕾上,晋A较其保持系明显缺少特征谱带,表明在此阶段雄性不育基因调控了同工酶的合成,导致花粉粒发生败育。

关键词: 晋A, 保持系, 酯酶, 过氧化物酶

Abstract: The PAGE analysis on JinA male sterile and its B-line of cotton showed that there were some re- sponsible bands of esterase and peroxidase for all tissues, and there were less differences in the same nutrient tis- sue part between them, which indicated that they had similar genetic background. Obvious differences were found due to the influence of male sterile genes, when entering reproduction stage, two isozymes of JinA were obvious less than that of B-line in dsporophyte-cell multiplicationd period, which showed that the male sterile genes controlled the synthesis of esterase and peroxidase isozymes, so the abortive pollens were informed.

Key words: JinA, B-line, Esterase, Peroxidase

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引用本文

李成奇, 石跃进, 潘转霞, 袁钧, 刘巷禄, 任雪峰. 棉花晋A及其保持系酯酶过氧化物酶PAGE电泳分析[J]. 华北农学报, 2004, 19(4): 11-13. doi: 10.3321/j.issn:1000-7091.2004.04.004.

LI Cheng-qi, SHI Yue-jin, PAN Zhuan-xia, YUAN Jun, LIU Xiang-lu, REN Xue-feng. PAGE Analysis on Esterase and Peroxidase of "JinA-line and B-line" in Cotton[J]. ACTA AGRICULTURAE BOREALI-SINICA, 2004, 19(4): 11-13. doi: 10.3321/j.issn:1000-7091.2004.04.004.

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