Jin Yoshinobu
Agro & Life Solutions Research Laboratory, Sumitomo Chemical Co., Ltd, Hyogo, Japan.
Anal Biochem. 2025 Feb;697:115723. doi: 10.1016/j.ab.2024.115723. Epub 2024 Nov 23.
Acetyl-CoA carboxylase (ACCase) is one of the most important enzymes as a herbicide target in gramineous plant species, however, assay methods for the enzyme are primarily limited to those using radioisotopes (RI). Typically, the measurement method that uses RI necessitates specialized facilities and equipment, and involves complex procedures throughout the experiment. As another method for detecting ACCase activity, the colorimetric method using malachite green (MG) is also known. However, reports on this method are limited, and information regarding the simplicity of the procedure and the scope of its application remains unclear. To better understand the method using MG and to develop a simpler assay method, crude enzymes extracted from various target-site resistant (TSR) biotypes of blackgrass (Alopecurus myosuroides) were examined in enzyme inhibition tests. As a result, this method was able to accurately detect the relationship between the chemical classes of ACC inhibitors and cross-resistance to specific TSRs. Moreover, the ACCase activity of other grass species was also examined using this method. By using crude enzymes from various species and a commercially available phosphatase kit containing MG, ACCase activity was detectable with good accuracy. In addition, enzyme inhibition studies using ACCase inhibiting herbicides revealed that this method reproduced results similar to those obtained with the RI method. The Z'-factor, an index of high-throughput screening (HTS), was around 0.7, indicating that it is an excellent screening system. These results suggest that the assay method using MG is very simple, labor-saving, and accurate with a throughput much higher than that of the existing RI method. Therefore, it is strongly suggested that the method could replace the RI method in most cases. These results indicate that it is applicable to HTS for ACCase inhibitors.
乙酰辅酶A羧化酶(ACCase)是禾本科植物中作为除草剂作用靶标的最重要酶之一,然而,该酶的测定方法主要局限于使用放射性同位素(RI)的方法。通常,使用RI的测量方法需要专门的设施和设备,并且在整个实验过程中涉及复杂的程序。作为检测ACCase活性的另一种方法,使用孔雀石绿(MG)的比色法也为人所知。然而,关于该方法的报道有限,其操作简便性和应用范围的相关信息仍不明确。为了更好地理解使用MG的方法并开发一种更简便的测定方法,我们在酶抑制试验中检测了从多花黑麦草(Alopecurus myosuroides)的各种靶标位点抗性(TSR)生物型中提取的粗酶。结果,该方法能够准确检测ACCase抑制剂的化学类别与对特定TSR的交叉抗性之间的关系。此外,还使用该方法检测了其他禾本科物种的ACCase活性。通过使用来自不同物种的粗酶和市售的含有MG的磷酸酶试剂盒,可以高精度地检测到ACCase活性。此外,使用抑制ACCase的除草剂进行的酶抑制研究表明,该方法得到的结果与RI方法相似。高通量筛选(HTS)指标Z'因子约为0.7,表明它是一个优秀的筛选系统。这些结果表明,使用MG的测定方法非常简单、省力且准确,通量比现有的RI方法高得多。因此,强烈建议该方法在大多数情况下可以取代RI方法。这些结果表明它适用于ACCase抑制剂的高通量筛选。