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木薯AGPase酶活性及其同工酶位点检测 被引量:3
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作者 闵义 王静 +2 位作者 姚远 胡新文 郭建春 《基因组学与应用生物学》 CAS CSCD 北大核心 2010年第2期298-302,共5页
本文以3个亲缘关系较远的高产木薯品种(SC124,SC8和Arg7)为材料,对块根发育过程中的AGPase活性和淀粉含量进行了测定,并利用AGPase同工酶电泳技术(非变性聚丙烯酰胺凝胶电泳)对AGPase酶活性较高时期同工酶位点进行检测,旨在分析木薯块根... 本文以3个亲缘关系较远的高产木薯品种(SC124,SC8和Arg7)为材料,对块根发育过程中的AGPase活性和淀粉含量进行了测定,并利用AGPase同工酶电泳技术(非变性聚丙烯酰胺凝胶电泳)对AGPase酶活性较高时期同工酶位点进行检测,旨在分析木薯块根AGPase同工酶位点与AGPase酶活性和淀粉积累的关系。结果表明:木薯块根发育过程中AGPase酶活性和淀粉含量呈极显著正相关(R=0.80212),Arg7的AGPase酶活性和淀粉含量在块根发育都显著高于SC124和SC8。同工酶分析表明,木薯至少有6个同工酶位点(AGPa,AGPb,AGPc,AGPd,AGPe和AGPf),且品种间具有多态性。其中,3个品种共有的4个同工酶位点分别为AGPa、AGPc、AGPd和AGPf,AGPe位点只在Arg7中出现,初步判断同工酶位点AGPe可能与其较高的酶活性和淀粉含量有关。本研究为系统研究木薯品种间AGPase酶活性与淀粉积累的关系提供了参考。 展开更多
关键词 木薯 腺苷二磷酸葡萄糖焦磷酸化(AGPase) 同工酶位点 活性 淀粉含量
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同工酶差异位点分析在蔬菜杂交种纯度检测中的应用 被引量:3
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作者 郑晓鹰 李丽 邢宝田 《生物技术通报》 CAS CSCD 2000年第3期29-33,共5页
用 10种同工酶和蛋白质分析体系 ,分析了 7种重要蔬菜的 71个杂交种与其亲本之间的差异位点以及这些差异位点用于杂交种纯度检测的可能性和存在的问题。试验表明 ,作物的不同种类 ,杂交种与亲本之间的亲缘关系以及作物种类的遗传多态性 ... 用 10种同工酶和蛋白质分析体系 ,分析了 7种重要蔬菜的 71个杂交种与其亲本之间的差异位点以及这些差异位点用于杂交种纯度检测的可能性和存在的问题。试验表明 ,作物的不同种类 ,杂交种与亲本之间的亲缘关系以及作物种类的遗传多态性 ,都会影响同工酶差异位点产生的多寡 ,从而影响到这一技术是否能用于此种作物的纯度检测。分析了不同同工酶在不同蔬菜中的多态性以及在蔬菜种子纯度检测中的表现。 展开更多
关键词 杂种纯度 蔬菜 同工差异位点 种子检验
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Genetic Analysis of Five Porphyra Species by Isozyme Markers
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作者 沈颂东 李艳燕 +4 位作者 许璞 张美如 袁昭兰 王建伟 朱建一 《Marine Science Bulletin》 CAS 2010年第1期65-78,共14页
Vertical polyamide gel electrophoresis was used to investigate isozyme polymorphisms among different isolates (including wild and cultivated) of Porphyra katadai, Porphyra oligospermatangia, Porphyra yezoensis, Porp... Vertical polyamide gel electrophoresis was used to investigate isozyme polymorphisms among different isolates (including wild and cultivated) of Porphyra katadai, Porphyra oligospermatangia, Porphyra yezoensis, Porphyra haitanensis, and a hybridize species (Porphyra yezoensis x Porphyra haitanensis) sampled from China. Whereafter, the analyses of probable minimum loci numbers, observed alleles sum, genetic diversity, and unweighted pair-group arithmetic average (UPGMA) cluster were carded out. After initial activity and resolution testing of bands of 23 enzymes, 6 of them (MDH, ME, LDH, GDH, IDH and G-6-PDH) were proved to be appropriate for analysis of the full sample set. The probable minimum numbers of loci and alleles analyses showed that the five species of Porphyra had an extraordinary consistent result in ME loci and alleles. However, P. katadai and P. oligospermatangia differed from other three species of Porphyra in LDH and GDH loci and alleles. P. katadai was independent in the analyses of MDH and P. oligosperTnatangia and P. haitanensis differed from other three species in IDH analyses. Moreover, P. yezoensis and P. haitanensis were apart from other three species in G-6-PDH analysis. Taking one with another, P. katadai was relatively separated in the probable minimum numbers of loci and alleles analyses. The results indicated that the genetic variation among the five Porphyra species was limited with a genetic identity of 0.7550. The hybridize species (P. yezoensis x P. haitanensis) seemed to be high homologue with P. oligospermatangia, unexpectedly got relatively lower average genetic identities with both P. yezoensis and P. haitanensis. The 4 strains of P. yezoensis were relatively divergent with an average genetic identity of 0.7428, and P. katadai presented the most differentiated, compared with other species, which consistented with the result summarized in the probable minimum numbers of loci and alleles analyses. 展开更多
关键词 PORPHYRA ISOZYME ALLELE gene locus genetic variety
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