Kato T, Tonomura Y
J Biochem. 1977 Jan;81(1):207-13. doi: 10.1093/oxfordjournals.jbchem.a131437.
Membranous vesicles (microsomes) were isolated from plasmodia of the acellular slime mold, Physarum polycephalum. The microsomes were about 0.2 about 0.2 micronM in diameter, and about 10 nm thick. The main protein component of the vesicles had a molecular weight of 100,000 daltons. Calcium ions were taken up by the microsomes only in the presence of Mg2+- ATP. The maximum amount of Ca2+ ions accumulated in the microsomes was 0.24 micronmole/mg protein. The Ca2+ uptake was not accelerated by oxalate. The ATPase [EC 3.6.1.3] activity required Ca2+ ions for full activation. The concentration of Ca2+ ions required for half-maximum activation was about 1 micronM. The Km and Vm values were 53 micronM and 1.6 micronmole/(mg-min), respectively. About 0.2 mole of Ca2+ ions was taken up by the microsomes, coupled with the hydrolysis of 1 mole of ATP. THE ATPase activity and Ca2+ uptake of the microsomes were not inhibited by sodium azide. Furthermore, electron microscopic examination showed that mitochondrial contamination was slight. These results suggest that a vesicular calcium transport system, analogous to the sacroplasmic reticulum in skeletal muscle, is involved in regulation of the Ca2+ concentration in plasmodia of Physarum.
从无细胞黏菌多头绒泡菌的原质团中分离出了膜泡(微粒体)。这些微粒体直径约为0.2微米,厚度约为10纳米。膜泡的主要蛋白质成分分子量为100,000道尔顿。只有在Mg2+-ATP存在的情况下,微粒体才会摄取钙离子。微粒体中积累的钙离子最大量为0.24微摩尔/毫克蛋白质。草酸盐不会加速钙离子的摄取。ATP酶[EC 3.6.1.3]的活性需要钙离子才能完全激活。半最大激活所需的钙离子浓度约为1微摩尔。Km和Vm值分别为53微摩尔和1.6微摩尔/(毫克·分钟)。微粒体摄取约0.2摩尔钙离子的同时伴随着1摩尔ATP的水解。微粒体的ATP酶活性和钙离子摄取不受叠氮化钠的抑制。此外,电子显微镜检查表明线粒体污染很轻微。这些结果表明,类似于骨骼肌肌浆网的囊泡钙转运系统参与了多头绒泡菌原质团中钙离子浓度的调节。