Hoehamer Christopher F, Mazur Chris S, Wolfe N L
National Research Council, U.S. Environmental Protection Agency, 960 College Station Road, Athens, Georgia 30605, USA.
J Agric Food Chem. 2005 Jan 12;53(1):90-7. doi: 10.1021/jf040329u.
An acid phosphatase from the aquatic plant Spirodela oligorrhiza (duckweed) was isolated by fast protein liquid chromatography and partially characterized. The enzyme was purified 1871-fold with a total yield of 40%. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) of the pure acid phosphatase resolved a single protein band that migrated to approximately 60 kDa. Nondenaturing SDS-PAGE electrophoresis revealed a single protein band around 120 kDa after staining with Coomassie Brilliant blue. Quantitative gel filtration chromatography estimated a native molecular mass of this enzyme to be 120 kDa. Thus, this acid phosphatase likely functions as a homodimer, consisting of two similar 60 kDa subunits. An electrophoretic technique using the flourogenic substrate 4-methylumbelliferyl phosphate enabled visualization of an acid phosphatase activity that corresponded to the protein band at 120 kDa on a nondenaturing PAGE gel. It was determined that the acid phosphatase had a pH optimum of 6.0 at 25 degrees C. The enzyme activity appeared to be stable over a broad range of temperatures (10-40 degrees C) and in the presence of the metals Zn2+, Mn2+, and Mg2+ as well as the chelating agents ethylenedinitrilotetraacetic acid and ethylene glycol tetraacetic acid. It was shown that this acid phosphatase could hydrolyze a variety of physiological organophosphate compounds including beta-glycerophosphate, phosphoserine, adenosine triphosphate, adenosine diphosphate, adenosine monphosphate, and pyrophosphate. Furthermore, analysis using capillary electrophoresis demonstrated that this hydrolytic enzyme could transform a wide array of organophosphate pesticides including S-2-ethylthioethyl O,O-dimethylphosphorothioate (demeton-S-methyl); S-1,2-bis(ethoxycarbonyl)ethyl O,O-dimethylphosphorodithioate (malathion); O,O-dimethyl O-4-nitrophenyl (paraoxon); O,O,O,O-tetraethyldithiopyrophosphate (sulfatep); O-2-chloro-4-nitrophenyl O,O-dimethylphosphorothioate (dicapthon); and 2,2-dichlorovinyl dimethylphosphate (dichlorvos).
通过快速蛋白质液相色谱法从水生植物少根紫萍(浮萍)中分离出一种酸性磷酸酶,并对其进行了部分特性鉴定。该酶经纯化后比活提高了1871倍,总产率为40%。纯酸性磷酸酶的十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)显示出一条单一的蛋白条带,迁移至约60 kDa处。非变性SDS-PAGE电泳经考马斯亮蓝染色后显示出一条约120 kDa的单一蛋白条带。定量凝胶过滤色谱法估计该酶的天然分子量为120 kDa。因此,这种酸性磷酸酶可能以同二聚体形式发挥作用,由两个相似的60 kDa亚基组成。一种使用荧光底物4-甲基伞形酮磷酸酯的电泳技术能够在非变性PAGE凝胶上可视化与120 kDa蛋白条带相对应的酸性磷酸酶活性。已确定该酸性磷酸酶在25℃时的最适pH为6.0。在较宽的温度范围(10 - 40℃)以及存在金属Zn2+、Mn2+和Mg2+以及螯合剂乙二胺四乙酸和乙二醇四乙酸的情况下,该酶活性似乎保持稳定。结果表明,这种酸性磷酸酶能够水解多种生理性有机磷酸化合物,包括β-甘油磷酸、磷酸丝氨酸、三磷酸腺苷、二磷酸腺苷、一磷酸腺苷和焦磷酸。此外,毛细管电泳分析表明,这种水解酶能够转化多种有机磷酸农药,包括S-2-乙硫基乙基O,O-二甲基硫代磷酸酯(甲基内吸磷);S-1,2-双(乙氧基羰基)乙基O,O-二甲基二硫代磷酸酯(马拉硫磷);O,O-二甲基O-4-硝基苯基(对氧磷);O,O,O,O-四乙基二硫代焦磷酸酯(硫代磷酸酯);O-2-氯-4-硝基苯基O,O-二甲基硫代磷酸酯(敌百虫);以及2,2-二氯乙烯基二甲基磷酸酯(敌敌畏)。