Kruse D, Cole G T
Department of Botany, University of Texas, Austin 78713-7640.
Infect Immun. 1992 Oct;60(10):4350-63. doi: 10.1128/iai.60.10.4350-4363.1992.
A beta-glucosidase of Coccidioides immitis was identified in electrophoresis gel separations of the concanavalin A-bound mycelial culture-filtrate-plus-lysate preparation. p-Nitrophenol-beta-D-glucopyranoside was used as the substrate to visualize the enzymatically active fraction in nonreducing gels. The gel-isolated, chromatographically purified enzyme has an optimal pH of 8.0 and cleaves beta-1,3-glycosyl linkages. The alkaline beta-glucosidase was further characterized by a pI of 3.8 to 4.0, optimal activity at 37 to 40 degrees C, and molecular size of 120 kDa as identified by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The purified beta-glucosidase is identical to a previously reported 120-kDa antigen (Ag) which reacts with immunoglobulin M (IgM) tube precipitin (TP) antibody in sera from patients with coccidioidomycosis. The TP-Ag was described as a valuable serodiagnostic reagent for detection of specific IgM in patients with early coccidioidal infections. The beta-glucosidase, like the TP-Ag, was localized in the cell wall and cytoplasmic vesicles of parasitic cells (spherules) by immunofluorescence and immunoelectron microscopy with specific antiserum raised against the purified enzyme. The boiled cell wall fraction isolated from these same young (presegmented) spherules was partially digested by the beta-glucosidase. Addition of a potent beta-glucosidase inhibitor, 1-deoxynojirimycin, to the parasitic-phase culture medium at a concentration of 200 microM blocked or retarded conversion of arthroconidia to spherules. Antibody was raised in guinea pigs against chromatographically purified 1-deoxynojirimycin which was conjugated with bovine serum albumin. The inhibitor was localized by immunofluorescence in the wall of the 1-deoxynojirimycin-treated cells. We suggest that the spherule wall-associated, alkaline hydrolase functions as a beta-1,3-glucanase to provide for wall plasticity as well as intussusception of newly synthesized wall polymers during the period of rapid diametric growth of parasitic cells of C. immitis.
在伴刀豆球蛋白A结合的菌丝体培养滤液加裂解物制剂的电泳凝胶分离中鉴定出了粗球孢子菌的一种β-葡萄糖苷酶。对硝基苯酚-β-D-吡喃葡萄糖苷用作底物,以在非还原凝胶中可视化酶活性部分。凝胶分离、色谱纯化的酶的最适pH为8.0,可裂解β-1,3-糖苷键。碱性β-葡萄糖苷酶的进一步特征为:通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳鉴定,其pI为3.8至4.0,在37至40℃具有最佳活性,分子大小为120 kDa。纯化的β-葡萄糖苷酶与先前报道的一种120 kDa抗原(Ag)相同,该抗原与球孢子菌病患者血清中的免疫球蛋白M(IgM)试管沉淀素(TP)抗体发生反应。TP-Ag被描述为用于检测早期球孢子菌感染患者中特异性IgM的一种有价值的血清学诊断试剂。与TP-Ag一样,通过用针对纯化酶产生的特异性抗血清进行免疫荧光和免疫电子显微镜观察,β-葡萄糖苷酶定位于寄生细胞(球形体)的细胞壁和细胞质小泡中。从这些相同的年轻(未分节)球形体中分离出的煮沸细胞壁部分被β-葡萄糖苷酶部分消化。以200 μM的浓度向寄生期培养基中添加一种有效的β-葡萄糖苷酶抑制剂1-脱氧野尻霉素,可阻断或延缓关节孢子向球形体的转化。用与牛血清白蛋白偶联的经色谱纯化的1-脱氧野尻霉素在豚鼠中制备抗体。通过免疫荧光在1-脱氧野尻霉素处理细胞的壁中定位该抑制剂。我们认为,与球形体壁相关的碱性水解酶作为一种β-1,3-葡聚糖酶发挥作用,以在粗球孢子菌寄生细胞快速直径生长期间提供壁的可塑性以及新合成壁聚合物的内填。