Zheleva D, Hankamer B, Barber J
Wolfson Laboratories, Department of Biochemistry, Imperial College of Science, Technology and Medicine, London, United Kingdom.
Biochemistry. 1996 Nov 26;35(47):15074-9. doi: 10.1021/bi961382h.
Photosystem II reaction centers (RC) isolated from peas (Pisum sativum L) purified by ionexchange chromatography were shown, by high-performance liquid chromatography (HPLC) size-exclusion analyses, to consist of a mixture of monomers (180 +/- 20 kDa) and dimers (390 +/- 35 kDa). Both fractions were resolved and purified by sucrose density gradient centrifugation and their homogeneity was demonstrated in size-exclusion HPLC elution profiles. Also present in the nonresolved preparation and the monomeric fraction were low levels of CP47 apoprotein (1.8% and 0.9% apoprotein of that found in a CP47-RC preparation). This CP47 contamination could maximally account for 0.41 and 0.22 Chl/RC, respectively, based on 22 chlorophylls being bound to each CP47 protein. The level of CP47 apoprotein was undetectable in the dimeric fractions. Pigment analysis using reverse-phase HPLC confirmed that contamination by chlorophyll bound to the CP47 apoprotein in the nonresolved RC preparation was low and that the ratio of chlorophyll a to pheophytin a remained 6 when the preparation was separated into its monomeric and dimeric components. We conclude, in agreement with earlier work, that the reaction center of PSII, when isolated using mild detergents and ion-exchange chromatography, contains 6 chlorophyll a/2 pheophytin a. We therefore do not concur with the recent published work of Pueyo et al. [(1995) Biochemistry 34, 15214-15218) that this type of preparation contains 4 chlorophyll a/2 pheophytin a and that the remaining 2 chlorophyll a are due to contamination by CP47.
通过离子交换色谱法从豌豆(Pisum sativum L)中分离纯化得到的光系统II反应中心(RC),经高效液相色谱(HPLC)尺寸排阻分析表明,其由单体(180±20 kDa)和二聚体(390±35 kDa)的混合物组成。通过蔗糖密度梯度离心对这两种组分进行了分离和纯化,并通过尺寸排阻HPLC洗脱图谱证明了它们的均一性。在未分离的制剂和单体组分中还存在低水平的CP47脱辅基蛋白(分别为CP47-RC制剂中发现的脱辅基蛋白的1.8%和0.9%)。基于每个CP47蛋白结合22个叶绿素,这种CP47污染最多分别占0.41和0.22 Chl/RC。在二聚体组分中未检测到CP47脱辅基蛋白的水平。使用反相HPLC进行的色素分析证实,未分离的RC制剂中与CP47脱辅基蛋白结合的叶绿素污染较低,并且当制剂分离为单体和二聚体组分时,叶绿素a与脱镁叶绿素a的比例仍为6。我们得出结论,与早期工作一致,当使用温和的去污剂和离子交换色谱法分离时,PSII的反应中心含有6个叶绿素a/2个脱镁叶绿素a。因此,我们不同意Pueyo等人最近发表的工作[(1995年)《生物化学》34卷,15214 - 15218页],即这种类型的制剂含有4个叶绿素a/2个脱镁叶绿素a,其余2个叶绿素a是由于CP47的污染。