Ogawa Naoto, Okamura Hideo, Hirai Hirofumi, Nishida Tomoaki
Department of Forest Resources Science, Faculty of Agriculture, Shizuoka University, Ohya 836, Shizuoka 422-8529, Japan.
Chemosphere. 2004 Apr;55(3):487-91. doi: 10.1016/j.chemosphere.2003.11.012.
Irgarol 1051 (2-methylthio-4-tert-butylamino-6-cyclopropylamino-s-triazine), a derivative of s-triazine herbicide, is an antifouling compound used as an alternative to organotins. The compound is highly persistent and is known to be biodegraded only by the white rot fungus, Phanerochaete chrysosporium. We used partially purified manganese peroxidase (MnP) prepared from P. chrysosporium to evaluate its capacity to degrade Irgarol 1051. MnP degraded Irgarol 1051 to two major products, one identified as M1 (identical to GS26575, 2-methylthio-4-tert-butylamino-6-amino-s-triazine) and the other not identified but with same mass spectrum as M1 and a different ultraviolet spectrum. This report clearly demonstrates that this ligninolytic enzyme is involved in the degradation of Irgarol 1051.
烯啶菌胺1051(2-甲硫基-4-叔丁氨基-6-环丙氨基-s-三嗪)是一种s-三嗪类除草剂的衍生物,是一种用作有机锡替代品的防污化合物。该化合物具有高度持久性,已知仅能被白腐真菌黄孢原毛平革菌生物降解。我们使用从黄孢原毛平革菌制备的部分纯化的锰过氧化物酶(MnP)来评估其降解烯啶菌胺1051的能力。MnP将烯啶菌胺1051降解为两种主要产物,一种鉴定为M1(与GS26575相同,即2-甲硫基-4-叔丁氨基-6-氨基-s-三嗪),另一种未鉴定,但质谱与M1相同,紫外光谱不同。本报告清楚地表明,这种木质素分解酶参与了烯啶菌胺1051的降解。