Yu J., Vermaas WFJ.
Department of Botany and the Center for the Study of Early Events in Photosynthesis, Arizona State University, Tempe, Arizona 85287-1601.
Plant Cell. 1990 Apr;2(4):315-322. doi: 10.1105/tpc.2.4.315.
After interruption or deletion of the photosystem II genes psbB, psbC, and psbD in the cyanobacterium Synechocystis sp. PCC 6803, thylakoids from such mutants were found to be depleted in a number of photosystem II proteins in addition to those for which the gene(s) had been inactivated. Transcript levels of photosystem II genes were measured and protein pulse-labeling was carried out to determine the reason for this effect. Transcripts of all photosystem II genes except the inactivated one(s) were found to be present in the various mutants. In certain cases, inactivation of one photosystem II gene led to overexpression of another. Protein pulse-labeling experiments using 35S-methionine, in which not only the rapidly turning over D1 protein but also D2, CP43, and CP47 appear to be preferentially labeled, showed that the mutants studied synthesize the D1 protein as well as other photosystem II proteins whose genes were not inactivated. The fact that, in the various mutants, photosystem II proteins for which the gene is not inactivated are synthesized but do not accumulate in the thylakoid indicates that the psbB, psbC, and psbD gene products are all required for a stable assembly of the photosystem II complex.
在蓝藻集胞藻PCC 6803中对光系统II基因psbB、psbC和psbD进行中断或缺失操作后,发现这些突变体的类囊体中,除了那些基因已失活的光系统II蛋白外,许多光系统II蛋白也减少了。对光系统II基因的转录水平进行了测量,并进行了蛋白质脉冲标记以确定这种效应的原因。发现除了失活的基因外,所有光系统II基因的转录本在各种突变体中均有存在。在某些情况下,一个光系统II基因的失活会导致另一个基因的过表达。使用35S-甲硫氨酸进行的蛋白质脉冲标记实验表明,所研究的突变体不仅能合成快速周转的D1蛋白,还能合成D2、CP43和CP47,而且这些蛋白似乎被优先标记,这表明突变体能够合成D1蛋白以及其他基因未失活的光系统II蛋白。在各种突变体中,基因未失活的光系统II蛋白能够合成,但不在类囊体中积累,这一事实表明,psbB、psbC和psbD基因产物对于光系统II复合物的稳定组装都是必需的。