Kreps J A, Town C D
Biology Department, Case Western Reserve University, Cleveland, Ohio 44106.
Plant Physiol. 1992 May;99(1):269-75. doi: 10.1104/pp.99.1.269.
Mutants of Arabidopsis thaliana have been selected for resistance to growth inhibition at the seedling stage by alpha-methyltryptophan (aMT). One mutant, amt-1 has been characterized in detail. The appearance and growth rate of the mutant in the absence of the inhibitor are similar to wild type, both as plants and callus. However, mutant plant growth is unaffected by 25 micromolar aMT and mutant callus growth by 50 micromolar aMT, concentrations that completely inhibit the growth of wild-type plants and callus, respectively. Tryptophan levels in mutant and wild-type plants are 24.3 +/- 2.7 and 4.7 +/- 1.2 micrograms per gram fresh weight, respectively, and in the corresponding callus 64.0 +/- 2.6 and 31.8 +/- 8.4 micrograms per gram fresh weight, respectively. Anthranilate synthase (AS) activity levels in crude extracts from whole plants are 3.09 +/- 0.54 nanomoles per milligram protein per hour in amt-1 and 1.32 +/- 0.21 nanomoles per milligram protein per hour in wild-type plants. In crude extracts from callus, anthranilate synthase levels are 11.54 +/- 2.05 nanomoles per milligram protein per hour and 7.74 +/- 1.58 in amt-1 and wild type, respectively. Enzyme extracts are inhibited by l-tryptophan; the concentrations required for 50% inhibition (I(50)) are 3.9 and 1.9 micromolar for amt-1 and for wild type, respectively. The mutation segregates as a single nuclear allele and shows incomplete dominance. The concomitant increases in both AS activity and its I(50) for tryptophan suggest that the mutation amt-1 either resides in one of the AS structural genes or causes increased expression of an AS isoform with an I(50) greater than the average for the entire extract.
已筛选出拟南芥对α-甲基色氨酸(aMT)在幼苗期生长抑制具有抗性的突变体。对其中一个突变体amt-1进行了详细表征。在没有抑制剂的情况下,该突变体作为植株和愈伤组织的外观及生长速率均与野生型相似。然而,25微摩尔的aMT对突变体植株生长无影响,50微摩尔的aMT对突变体愈伤组织生长无影响,而这两个浓度分别能完全抑制野生型植株和愈伤组织的生长。突变体和野生型植株中色氨酸水平分别为每克鲜重24.3±2.7微克和4.7±1.2微克,相应愈伤组织中分别为每克鲜重64.0±2.6微克和31.8±8.4微克。全株粗提物中邻氨基苯甲酸合酶(AS)的活性水平在amt-1中为每毫克蛋白质每小时3.09±0.54纳摩尔,在野生型植株中为每毫克蛋白质每小时1.32±0.21纳摩尔。在愈伤组织粗提物中,amt-1和野生型中邻氨基苯甲酸合酶水平分别为每毫克蛋白质每小时11.54±2.05纳摩尔和7.74±1.58纳摩尔。酶提取物受到L-色氨酸的抑制;50%抑制所需的浓度(I(50))在amt-1和野生型中分别为3.9微摩尔和1.9微摩尔。该突变作为单个核等位基因分离,表现出不完全显性。AS活性及其对色氨酸的I(50)同时增加表明,突变体amt-1要么位于AS结构基因之一中,要么导致具有大于整个提取物平均值的I(50)的AS同工型表达增加。