Fujii I, Iwabuchi Y, Teshima T, Shiba T, Kikuchi M
Protein Engineering Research Institute, Osaka, Japan.
Bioorg Med Chem. 1993 Aug;1(2):147-9. doi: 10.1016/s0968-0896(00)82112-4.
A chromogenic substrate 1, 5-bromo-4-chloroindol-3-yl 5-acetamido-3,5-dideoxy-alpha-D-glycero-D-galacto-2-nonulopyranosidon ic acid (X-Neu5Ac), has been synthesized to facilitate the screening of bacterial colonies or plaques for the detection of either natural or mutant neuraminidase activity. Substrate 1 was hydrolyzed by neuraminidase isolated from Clostridium perfringens to release a halogenated indol-3-ol 2 that undergoes rapid aerobic oxidation to form the dark blue pigment, 5,5'-dibromo-4,-4'-dichloroindigo 3. Preliminary kinetic studies indicate that this compound is a good substrate (Km 0.89 x 10(-3) M) for neuraminidase and is quite stable under identical conditions in the absence of enzyme. These results suggest that X-Neu5Ac 1 can be useful to screen for bacterially-encoded enzyme production directly on agar plates.
已合成一种显色底物1,5-溴-4-氯吲哚-3-基5-乙酰氨基-3,5-二脱氧-α-D-甘油-D-半乳糖-2-壬酮吡喃糖苷酸(X-Neu5Ac),以促进对细菌菌落或噬菌斑的筛选,用于检测天然或突变的神经氨酸酶活性。底物1被从产气荚膜梭菌分离的神经氨酸酶水解,释放出卤代吲哚-3-醇2,其经历快速需氧氧化形成深蓝色色素5,5'-二溴-4,4'-二氯靛蓝3。初步动力学研究表明,该化合物是神经氨酸酶的良好底物(Km为0.89×10⁻³ M),并且在无酶的相同条件下相当稳定。这些结果表明,X-Neu5Ac 1可用于直接在琼脂平板上筛选细菌编码的酶的产生。