Shen G, Vermaas W F
Department of Botany, Arizona State University, Tempe 85287-1601.
J Biol Chem. 1994 May 13;269(19):13904-10.
The chlorophyll protein organization has been investigated in thylakoid membranes from mutants of the cyanobacterium Synechocystis sp. PCC 6803, in which the photosystem II (PS II) genes psbB and/or psbC (coding for CP47 and CP43, respectively) were inactivated together with the psaAB operon (coding for the photosystem I (PS I) core complex) and the apcE gene (coding for the phycobilisome anchor protein). Lack of the CP43 protein led to a significant decrease of the D1, D2, and CP47 proteins and a decrease in the 77 K fluorescence emission peak at 685 nm. In the absence of the CP47 protein, no PS II reaction center assembly was detected and the 77 K fluorescence emission peak at 695 nm was lost. The psbB-/psbC-/PS I-less/apcE- mutant had no assembly of the D1, D2, CP47, and CP43 proteins, had lost the 77 K fluorescence emission peaks at 685 and 695 nm, but retained about 15% of the chlorophyll present in the PS I-less/apcE- background strain. A broad 77 K fluorescence emission band with a maximum at 678 nm was displayed in the PS II-less, PS I-less mutant upon excitation of the remaining chlorophyll. A 678 nm shoulder was observed in the 77 K fluorescence emission spectrum of thylakoids from the psbB-/PS I-less/apcE- mutant, which still contains CP43 but no PS II reaction center. This shoulder was absent in thylakoids from the psbC-/PS I-less/apcE- mutant, which contain some PS II reaction center complexes. These results are consistent with the chlorophyll associated with the 678 nm emission to serve as peripheral antenna to PS II. The fluorescence emission characteristics of this chlorophyll are different from those of an accessory chlorophyll-binding protein expressed under iron-stress conditions in cyanobacteria. The chlorophyll remaining in the absence of PS II and PS I is indicative of a new chlorophyll-binding protein in cyanobacterial thylakoids.
对集胞藻6803(Synechocystis sp. PCC 6803)蓝细菌突变体类囊体膜中的叶绿素蛋白组织进行了研究。在这些突变体中,光系统II(PS II)基因psbB和/或psbC(分别编码CP47和CP43)与psaAB操纵子(编码光系统I(PS I)核心复合物)以及apcE基因(编码藻胆体锚定蛋白)一起失活。缺乏CP43蛋白导致D1、D2和CP47蛋白显著减少,并且685 nm处的77 K荧光发射峰降低。在缺乏CP47蛋白的情况下,未检测到PS II反应中心组装,并且695 nm处的77 K荧光发射峰消失。psbB - /psbC - /PS I缺失/apcE - 突变体没有D1、D2、CP47和CP43蛋白的组装,失去了685和695 nm处的77 K荧光发射峰,但保留了PS I缺失/apcE - 背景菌株中约15%的叶绿素。在剩余叶绿素激发后,PS II缺失、PS I缺失的突变体中显示出一个在678 nm处有最大值的宽77 K荧光发射带。在psbB - /PS I缺失/apcE - 突变体的类囊体77 K荧光发射光谱中观察到一个678 nm的肩峰,该突变体仍含有CP43但没有PS II反应中心。在含有一些PS II反应中心复合物的psbC - /PS I缺失/apcE - 突变体的类囊体中,这个肩峰不存在。这些结果与与678 nm发射相关的叶绿素作为PS II的外周天线一致。这种叶绿素的荧光发射特性与蓝细菌在铁胁迫条件下表达的一种辅助叶绿素结合蛋白的荧光发射特性不同。在没有PS II和PS I的情况下剩余的叶绿素表明蓝细菌类囊体中存在一种新的叶绿素结合蛋白。