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Soybean Roots Retain the Seed Urease Isozyme Synthesized during Embryo Development

机译:大豆根保留了胚发育过程中合成的种子脲酶同工酶

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摘要

Roots of young soybean (Glycine max [L.] Merr.) plants (up to 25 days old) contain two distinct urease isozymes, which are separable by hydroxyapatite chromatography. These two urease species (URE1 and URE2) differ in: (a) electrophoretic mobility in native gels, (b) pH dependence, and (c) recognition by a monoclonal antibody specific for the seed (“embryo-specific”) urease. By these parameters root URE1 urease is similar to the abundant embryo-specific urease isozyme, while root URE2 resembles the “ubiquitous” urease which has previously been found in all soybean tissues examined (leaf, embryo, seed coat, and cultured cells). The embryo-specific and ubiquitous urease isozymes are products of the Eu1 and Eu4 structural genes, respectively. Roots of the eu1-sun/eu1-sun genotype, which lacks the embryo-specific urease (i.e. `seed urease-null'), contain no URE1 urease activity. Roots of eu4/eu4, which lacks ubiquitous urease, lack the URE2 (leaflike) urease activity. From these genetic and biochemical criteria, then, we conclude that URE1 and URE2 are the embryo-specific and ubiquitous ureases, respectively. Adventitious roots generated from cuttings of any urease genotype lack URE1 activity. In seedling roots the seedlike (URE1) activity declines during development. Roots of 3-week-old plants contain 5% of the total URE1 activity of the radicle of 4-day-old seedlings, which, in turn, has approximately the same urease activity level as the dormant embryonic axis. The embryo-specific urease incorporates label from [35S]methionine during embryo development but not during germination, indicating that there is no de novo synthesis of the embryo-specific (URE1) urease in the germinating root. We conclude that the seedlike urease (URE1) found in roots of young soybean plants is a remnant of the Eu1-encoded, abundant, embryo-specific urease which accumulates in the embryonic root axis during seed development.
机译:幼小大豆(Glycine max [L.] Merr。)植物(长达25天大)的根中含有两种不同的脲酶同工酶,可通过羟磷灰石色谱法分离。这两种脲酶(URE1和URE2)的不同之处在于:(a)天然凝胶中的电泳迁移率,(b)pH依赖性,以及(c)对种子(“胚胎特异性”)脲酶具有特异性的单克隆抗体识别。通过这些参数,根URE1脲酶类似于丰富的胚胎特异性脲酶同工酶,而根URE2类似于先前在所有检查的大豆组织(叶,胚,种皮和培养细胞)中都发现的“普遍存在”脲酶。胚胎特异性和普遍存在的脲酶同工酶分别是Eu1和Eu4结构基因的产物。 eu1-sun / eu1-sun基因型的根缺乏胚特异性脲酶(即“种子脲酶零”),没有URE1脲酶活性。 eu4 / eu4的根缺乏普遍存在的脲酶,而缺乏URE2(叶状)脲酶活性。从这些遗传和生化标准,然后,我们得出结论,URE1和URE2分别是胚胎特异性尿素酶和普遍存在的脲酶。由任何脲酶基因型的插条产生的不定根缺乏URE1活性。在幼苗的根中,类种子(URE1)活性在发育过程中下降。 3周龄植物的根系占4天龄幼苗胚根总URE1活性的5%,而后者具有与休眠胚轴大致相同的脲酶活性水平。胚胎特异性脲酶在胚胎发育过程中掺入了来自[ 35 S]蛋氨酸的标签,但在发芽过程中并未掺入,这表明发芽的根中没有从头合成胚胎特异性(URE1)脲酶。我们得出的结论是,在年轻大豆植株的根中发现的类种子脲酶(URE1)是Eu1编码的,丰富的,特定于胚的脲酶的残留物,该酶在种子发育过程中累积在胚根轴中。

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