Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06504.
Plant Physiol. 1980 Aug;66(2):334-41. doi: 10.1104/pp.66.2.334.
Seven lines of haploid Nicotiana tabacum tissue culture selected for resistance to normally toxic levels of the glycine analog glycine hydroxamate, a competitive inhibitor of the glycine decarboxylase reaction, were investigated. The presence of glycine hydroxamate greatly increased the intracellular concentration of both glycine and alanine in wild type and resistant cell lines, suggesting that the inhibitor blocks both glycine- and alanine-utilizing reactions. All the resistant cell lines, whether grown in the presence or absence of glycine hydroxamate, had high intracellular concentrations of the 12 free amino acids which were analyzed, including glycine and serine. (These lines averaged 3.6 times the total amino acid content of wild-type cells in the absence of the inhibitor). The resistant cell lines were indistinguishable from wild-type cell lines in their metabolism of radioactively labeled glycine hydroxamate and glycine. Comparison of the metabolism of radioactively labeled alanine, glycolate, and glyoxylate in wild-type and alpha resistant line also revealed no distinctive differences. Glycine decarboxylase activities were unaltered in the resistant cell lines. The cellular toxicity of glycine hydroxamate is considered in relation to (1) the competitive inhibition by glycine hydroxamate of the glycine- and alanine-utilizing enzymes and (2) the resultant imbalances caused by high intracellular concentrations of these amino acids. The significance of elevation of total free amino acid concentration in effecting resistance to the inhibitor is discussed.Plants were regenerated from 5 of these lines and callus cultures of explants were tested for glycine hydroxamate resistance. Plants from seedlings of two lines which retained the resistant characteristic in explanted callus did not have high amino acid levels in leaves.
选择了七条单倍体烟草组织培养物,这些培养物对甘氨酸类似物草酰氨的正常毒性水平具有抗性,草酰氨是甘氨酸脱羧酶反应的竞争性抑制剂。在野生型和抗性细胞系中,草酰氨的存在大大增加了甘氨酸和丙氨酸的细胞内浓度,这表明抑制剂阻断了甘氨酸和丙氨酸利用反应。所有抗性细胞系,无论是在存在还是不存在草酰氨的情况下生长,都具有高水平的 12 种游离氨基酸,包括甘氨酸和丝氨酸。(这些细胞系在没有抑制剂的情况下,平均比野生型细胞系的总氨基酸含量高 3.6 倍)。抗性细胞系在代谢放射性标记的草酰氨和甘氨酸方面与野生型细胞系没有区别。在野生型和 alpha 抗性系中,放射性标记的丙氨酸、乙二醇酸盐和乙醛酸盐的代谢比较也没有显示出明显的差异。抗性细胞系中的甘氨酸脱羧酶活性没有改变。草酰氨的细胞毒性与(1)草酰氨对甘氨酸和丙氨酸利用酶的竞争性抑制作用以及(2)这些氨基酸在细胞内浓度升高引起的不平衡有关。讨论了总游离氨基酸浓度升高对抵抗抑制剂的意义。从其中的 5 个系中再生了植物,并测试了外植体愈伤组织对草酰氨的抗性。在保留了外植体愈伤组织抗性特征的两个系的幼苗中再生的植物叶片中没有高氨基酸水平。