Douma A C, Veenhuis M, Sulter G J, Waterham H R, Verheyden K, Mannaerts G P, Harder W
Department of Microbiology, University of Groningen, Haren, The Netherlands.
Arch Microbiol. 1990;153(5):490-5. doi: 10.1007/BF00248432.
We have studied the permeability properties of intact peroxisomes and purified peroxisomal membranes from two methylotrophic yeasts. After incorporation of sucrose and dextran in proteoliposomes composed of asolectin and peroxisomal membranes isolated from the yeasts Hansenula polymorpha and Candida boidinii a selective leakage of sucrose occurred indicating that the peroxisomal membranes were permeable to small molecules. Since the permeability of yeast peroxisomal membranes in vitro may be due to the isolation procedure employed, the osmotic stability of peroxisomes was tested during incubations of intact protoplasts in hypotonic media. Mild osmotic swelling of the protoplasts also resulted in swelling of the peroxisomes present in these cells but not in a release of their matrix proteins. The latter was only observed when the integrity of the cells was disturbed due to disruption of the cell membrane during further lowering of the concentration of the osmotic stabilizer. Stability tests with purified peroxisomes indicated that this leak of matrix proteins was not associated with the permeability to sucrose. Various attempts to mimic the in vivo situation and generate a proton motive force across the peroxisomal membranes in order to influence the permeability properties failed. Two different proton pumps were used for this purpose namely bacteriorhodopsin (BR) and reaction center-light-harvesting complex I (RCLH1 complex). After introduction of BR into the membrane of intact peroxisomes generation of a pH-gradient was not or barely detectable. Since this pump readily generated a pH-gradient in pure liposomes, these results strengthened the initial observations on the leakiness of the peroxisomal membrane fragments.(ABSTRACT TRUNCATED AT 250 WORDS)
我们研究了来自两种甲基营养型酵母的完整过氧化物酶体和纯化的过氧化物酶体膜的通透性特性。在将蔗糖和葡聚糖掺入由大豆卵磷脂和从多形汉逊酵母和博伊丁假丝酵母分离的过氧化物酶体膜组成的蛋白脂质体后,蔗糖发生选择性渗漏,表明过氧化物酶体膜对小分子具有通透性。由于体外酵母过氧化物酶体膜的通透性可能归因于所采用的分离程序,因此在低渗培养基中完整原生质体孵育期间测试了过氧化物酶体的渗透稳定性。原生质体的轻度渗透性肿胀也导致这些细胞中存在的过氧化物酶体肿胀,但不会释放其基质蛋白。只有当渗透压稳定剂浓度进一步降低期间细胞膜破裂导致细胞完整性受到干扰时,才会观察到后者。用纯化的过氧化物酶体进行的稳定性测试表明,这种基质蛋白的泄漏与对蔗糖的通透性无关。为了影响通透性特性,进行了各种模拟体内情况并在过氧化物酶体膜上产生质子动力势的尝试,但均未成功。为此使用了两种不同的质子泵,即细菌视紫红质(BR)和反应中心-光捕获复合体I(RCLH1复合体)。将BR引入完整过氧化物酶体膜后,未检测到或几乎检测不到pH梯度的产生。由于该泵在纯脂质体中很容易产生pH梯度,这些结果强化了对过氧化物酶体膜片段渗漏性的初步观察。(摘要截短至250字)