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矮牵牛硝酸还原酶缺陷突变体的生化和遗传特征。

Biochemical and genetical characterization of nitrate reductase deficient mutants of Petunia.

机构信息

Max-Planck-Institut für Züchtungsforschung (Erwin-Baur-Institut), D-5000, Köln 30, Federal Republic of Germany.

出版信息

Plant Cell Rep. 1984 Aug;3(4):134-7. doi: 10.1007/BF00270206.

Abstract

Four NR(-) lines were selected by their resistance to 100 mM chlorate from X-ray irradiated protoplasts of haploid Petunia hybrida var. Mitchell. The four cell lines were characterized by the presence of xanthine dehydrogenase activity and by complementation tests via protoplast fusion. One mutant (line 1) was classified as defective in the NR apoprotein (tentatively, nia-type) and the other three (lines 2, 3, 4) in the molybdenum cofactor (tentatively, cnx-type). Some NR activity (15 %) could be restored by adding unphysiologically high concentrations of molybdate to the culture medium in two of the cnx-lines (lines 3 and 4). The third cnx-line (line 2) had no NR activity. A complementation analysis via protoplast fusion confirmed that the mutants comprised 3 non-allelic groups. From these results it can be concluded that these NR(-) mutants are recessive and that two of the cnx-mutants (lines 3, 4) are allelic.

摘要

从经 X 射线处理的矮牵牛(Petunia hybrida var. Mitchell)原生质体中筛选出 4 株对 100mM 氯酸盐有抗性的 NR(-)系。这 4 个细胞系的特征是存在黄嘌呤脱氢酶活性,并通过原生质体融合进行互补测试。一个突变体(系 1)被归类为 NR 脱辅基蛋白缺陷(暂定,nia 型),另外 3 个(系 2、3、4)为钼辅因子缺陷(暂定,cnx 型)。在两个 cnx 系(系 3 和系 4)中,通过向培养基中添加非生理浓度的钼酸盐,可以部分恢复 NR 活性(15%)。第三个 cnx 系(系 2)没有 NR 活性。通过原生质体融合的互补分析证实,这些突变体包含 3 个非等位基因群。根据这些结果可以得出结论,这些 NR(-)突变体是隐性的,其中两个 cnx 突变体(系 3、4)是等位基因。

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