Laboratoire de Mycologie associé au CNRS, Laboratoire de Physiologie Végétale, Université Lyon 1, 43 Boulevard du 11 Novembre 1918, F-69622, Villeurbanne Cedex, France.
Planta. 1984 Apr;160(5):400-6. doi: 10.1007/BF00429755.
Cytoplasmic membranes from mycelium or protoplasts of Saprolegnia monoica (a cellulosic cell-wall fungus) were separated by continuous sucrose-density-gradient centrifugation. Glucan synthases assayed at low (micromolar uridine 5'-diphosphate (UDP) glucose for β-1-4-glucan synthase) and high (millimolar UDP glucose for β-1-3-glucan synthase) substrate concentrations were associated with membranes exhibiting vanadate-sensitive, oligomycin-insensitive ATPase and equilibrating at density 1.16 g cm(-3). Synthase activities were also bound to membranes of lower density (1.10 and 1.145 g cm(-3)). Plasma membranes were stabilized by coating protoplasts with concanavalin A. After lysis of the protoplasts, plasma membranes recovered by low centrifugal forces were isolated in continuous isopycinic gradients. Both synthase activities peaked with [(3)H]concanavalin A and Na-vanadate ATPase indicating that the synthetases are located at the plasma membrane. Treatments of intact protoplasts with cold glutaraldehyde or proteases before disruption lead to a diminution of glucan-synthase activities indicating that at least part of the enzymes of plasma membrane face the outside of the cell.
从单毛藻(一种纤维素细胞壁真菌)的菌丝体或原生质体中分离出的细胞质膜,通过连续蔗糖密度梯度离心分离。在低(微摩尔尿嘧啶 5'-二磷酸(UDP)葡萄糖用于β-1-4-葡聚糖合酶)和高(毫摩尔 UDP 葡萄糖用于β-1-3-葡聚糖合酶)底物浓度下测定的葡聚糖合酶与表现出钒酸盐敏感、寡霉素不敏感 ATP 酶并在密度 1.16 g cm(-3)处平衡的膜相关联。合酶活性也与密度较低的膜(1.10 和 1.145 g cm(-3))结合。通过用刀豆球蛋白 A 涂覆原生质体来稳定质膜。在用低离心力裂解原生质体后,通过连续等密度梯度分离回收质膜。两种合酶活性均与[(3)H]刀豆球蛋白 A 和 Na-钒酸盐 ATP 酶的峰值相一致,表明这些合酶位于质膜上。在破坏之前,用冷戊二醛或蛋白酶处理完整的原生质体,导致葡聚糖合酶活性降低,表明至少部分质膜酶面向细胞的外部。