DowElanco, Walnut Creek, California 94598.
Plant Physiol. 1990 Sep;94(1):239-44. doi: 10.1104/pp.94.1.239.
Triazolopyrimidine sulfanilides are a class of highly active herbicides whose primary target is acetolactate synthase. Spontaneous mutants of tobacco (Nicotiana tabacum) (KS-43) and cotton (Gossypium hirsutum) (PS-3 and DO-2) resistant to triazolopyrimidine sulfonanilide were selected in tissue culture. Acetolactate synthase partially purified from the three mutants were 80- to 1000-fold less sensitive to inhibition by the compound compared with the corresponding wild-type enzyme. The mutants also varied in the cross-resistance pattern to other acetolactate synthase inhibiting herbicides in the sulfonylurea, imidazolinone, and pyrimidyl-oxy-benzoate chemical families. Thus, acetolactate synthase from KS-43, PS-3, and DO-2 cultures have different mutations. The affinities for pyruvate, thiamine pyrophosphate, as well as the activity of the mutant enzymes were found to be comparable to the corresponding wild-type enzymes. However, the enzyme from PS-3 was highly resistant to feedback inhibition by valine and leucine. In contrast, acetolactate synthase from KS-43 and DO-2 were inhibited by valine and leucine to nearly the same extent as the wild-type enzymes. Also, PS-3 cultures accumulated much higher levels of the branched chain amino acids compared to the wild-type cotton culture. The mutation in the PS-3 enzyme has therefore rendered it insensitive to feedback regulation by valine and leucine.
三唑并嘧啶磺酰脲类是一类高效除草剂,其主要靶标是乙酰乳酸合成酶。在组织培养中选择了对三唑并嘧啶磺酰脲类具有抗性的烟草(Nicotiana tabacum)(KS-43)和棉花(Gossypium hirsutum)(PS-3 和 DO-2)自发突变体。从这三个突变体中部分纯化的乙酰乳酸合成酶对该化合物的抑制作用比对相应的野生型酶的抑制作用低 80-1000 倍。突变体对磺酰脲类、咪唑啉酮类和嘧啶氧基苯甲酸类中其他乙酰乳酸合成酶抑制剂类除草剂的交叉抗性模式也有所不同。因此,KS-43、PS-3 和 DO-2 培养物中的乙酰乳酸合成酶有不同的突变。发现丙酮酸、硫胺素焦磷酸的亲和力以及突变酶的活性与相应的野生型酶相当。然而,来自 PS-3 的酶对缬氨酸和亮氨酸的反馈抑制具有高度抗性。相比之下,KS-43 和 DO-2 的乙酰乳酸合成酶对缬氨酸和亮氨酸的抑制作用与野生型酶相当。此外,PS-3 培养物中支链氨基酸的积累水平比野生型棉花培养物高得多。因此,PS-3 酶的突变使其对缬氨酸和亮氨酸的反馈调节不敏感。