Koike Hiroyuki, Ikeda Yohei, Yusa Fumie, Kashino Yasuhiro, Satoh Kazuhiko
Department of Life Science, Graduate School of Life Science, University of Hyogo, Ako, Hyogo 678-1297, Japan.
Photosynth Res. 2007 Jul-Sep;93(1-3):45-53. doi: 10.1007/s11120-007-9156-2. Epub 2007 Jun 29.
Envelope membranes were isolated by sucrose density gradient floatation centrifugation from the homogenate of cyanelles prepared from Cyanophora paradoxa. Two yellow bands were separated after 40 h of centrifugation. The buoyant density of one of the two fractions (fraction Y2) coincided with that of inner envelope membranes of spinach or plasma membranes of cyanobacteria. The other yellow fraction (fraction Y1) migrated to top of sucrose-gradient even at 0% sucrose. Pigment analysis revealed that the heavy yellow fraction was rich in zeaxanthin while the light fraction was rich in beta-carotene, and the both fractions contained practically no chlorophylls. Another yellow fraction (fraction Y3) was isolated from the phycobiliprotein fraction, which was the position where the sample was placed for gradient centrifugation. Its buoyant density and absorption spectra were similar to outer membranes of cyanobacteria. We have assigned fractions Y2 and Y3 as inner and outer envelope membrane fractions of cyanelles, respectively. Protein compositions were rather different between the two envelope membranes indicating little cross-contamination among the fractions.
通过蔗糖密度梯度漂浮离心法,从蓝氏原绿藻制备的蓝小体匀浆中分离出包膜膜。离心40小时后分离出两条黄色带。这两个组分之一(组分Y2)的浮力密度与菠菜内膜或蓝细菌质膜的浮力密度一致。另一个黄色组分(组分Y1)即使在0%蔗糖的情况下也迁移到蔗糖梯度的顶部。色素分析表明,重黄色组分富含玉米黄质,而轻组分富含β-胡萝卜素,且两个组分几乎都不含叶绿素。从藻胆蛋白组分中分离出另一个黄色组分(组分Y3),该组分是样品进行梯度离心时的放置位置。其浮力密度和吸收光谱与蓝细菌的外膜相似。我们分别将组分Y2和Y3指定为蓝小体的内膜和外膜组分。两种包膜膜之间的蛋白质组成差异很大,表明各组分之间几乎没有交叉污染。