Nagasawa T, Ryuno K, Yamada H
Biochem Biophys Res Commun. 1986 Sep 30;139(3):1305-12. doi: 10.1016/s0006-291x(86)80320-5.
Nitrile hydratase was purified and crystallized from the crude extract of Brevibacterium R312 and found to be homogeneous by the results of disc gel electrophoresis, analytical ultracentrifuge and double diffusion in agarose. The enzyme has a molecular mass of about 85,000 Da and contains approximately 3 g atoms iron/mol enzyme. The enzyme was composed of two kinds of subunits, of which molecular masses were 26,000 Da and 27,500 Da. The concentrated solution of the enzyme had a pronounced greyish green color and exhibited a broad absorption in visible range with a absorption maxima at 712 nm. The enzyme was active toward various aliphatic nitriles.
腈水合酶从短杆菌R312的粗提物中纯化并结晶,通过圆盘凝胶电泳、分析超速离心和琼脂糖双扩散结果表明其具有均一性。该酶的分子量约为85,000道尔顿,每摩尔酶含有约3克原子铁。该酶由两种亚基组成,其分子量分别为26,000道尔顿和27,500道尔顿。酶的浓缩溶液呈现出明显的灰绿色,在可见光范围内有较宽的吸收峰,最大吸收波长为712纳米。该酶对各种脂肪族腈具有活性。