Siehl D L, Subramanian M V, Walters E W, Lee S F, Anderson R J, Toschi A G
Sandoz Agro, Inc., Research Division, Palo Alto, California 94304-1104, USA.
Plant Physiol. 1996 Mar;110(3):753-8. doi: 10.1104/pp.110.3.753.
The site of action of hydantocidin was probed using Arabidopsis thaliana plants growing on agar plates. Herbicidal effects were reversed when the agar medium was supplemented with AMP, but not IMP or GMP, suggesting that hydantocidin blocked the two-step conversion of IMP to AMP in the de novo purine biosynthesis pathway. Hydantocidin itself did not inhibit adenylosuccinate synthetase or adenylosuccinate lyase isolated from Zea mays. However, a phosphorylated derivative of hydantocidin, N-acetyl-5'-phosphohydantocidin, was a potent inhibitor of the synthetase but not of the lyase. These results identify the site of action of hydantocidin and establish adenylosuccinate synthetase as an herbicide target of commercial potential.
利用生长在琼脂平板上的拟南芥植株探究了稻瘟菌素的作用位点。当在琼脂培养基中添加AMP而非IMP或GMP时,除草效果会逆转,这表明稻瘟菌素在从头嘌呤生物合成途径中阻断了IMP向AMP的两步转化。稻瘟菌素本身并不抑制从玉米中分离出的腺苷酸琥珀酸合成酶或腺苷酸琥珀酸裂解酶。然而,稻瘟菌素的一种磷酸化衍生物N-乙酰-5'-磷酸稻瘟菌素是该合成酶的有效抑制剂,但不是裂解酶的抑制剂。这些结果确定了稻瘟菌素的作用位点,并将腺苷酸琥珀酸合成酶确立为具有商业潜力的除草剂靶点。