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集胞藻6803中光系统I多肽的突变分析。psaI的靶向失活揭示了psaI在psaL结构组织中的功能。

Mutational analysis of photosystem I polypeptides in the cyanobacterium Synechocystis sp. PCC 6803. Targeted inactivation of psaI reveals the function of psaI in the structural organization of psaL.

作者信息

Xu Q, Hoppe D, Chitnis V P, Odom W R, Guikema J A, Chitnis P R

机构信息

Division of Biology, Kansas State University, Manhattan 66506-4901, USA.

出版信息

J Biol Chem. 1995 Jul 7;270(27):16243-50. doi: 10.1074/jbc.270.27.16243.

Abstract

We cloned, characterized, and inactivated the psaI gene encoding a 4-kDa hydrophobic subunit of photosystem I from the cyanobacterium Synechocystis sp. PCC 6803. The psaI gene is located 90 base pairs downstream from psaL, and is transcribed on 0.94- and 0.32-kilobase transcripts. To identify the function of PsaI, we generated a cyanobacterial strain in which psaI has been interrupted by a gene for chloramphenicol resistance. The wild-type and the mutant cells showed comparable rates of photoautotrophic growth at 25 degrees C. However, the mutant cells grew slower and contained less chlorophyll than the wild-type cells, when grown at 40 degrees C. The PsaI-less membranes from cells grown at either temperature showed a small decrease in NADP+ photoreduction rate when compared to the wild-type membranes. Inactivation of psaI led to an 80% decrease in the PsaL level in the photosynthetic membranes and to a complete loss of PsaL in the purified photosystem I preparations, but had little effect on the accumulation of other photosystem I subunits. Upon solubilization with nonionic detergents, photosystem I trimers could be obtained from the wild-type, but not from the PsaI-less membranes. The PsaI-less photosystem I monomers did not contain detectable levels of PsaL. Therefore, a structural interaction between PsaL and PsaI may stabilize the association of PsaL with the photosystem I core. PsaL in the wild-type and PsaI-less membranes showed equal resistance to removal by chaotropic agents. However, PsaL in the PsaI-less strain exhibited an increased susceptibility to proteolysis. From these data, we conclude that PsaI has a crucial role in aiding normal structural organization of PsaL within the photosystem I complex and the absence of PsaI alters PsaL organization, leading to a small, but physiologically significant, defect in photosystem I function.

摘要

我们克隆、鉴定并使来自集胞藻6803(Synechocystis sp. PCC 6803)的编码光系统I 4 kDa疏水亚基的psaI基因失活。psaI基因位于psaL下游90个碱基对处,转录产生0.94 kb和0.32 kb的转录本。为了确定PsaI的功能,我们构建了一个蓝藻菌株,其中psaI被氯霉素抗性基因打断。野生型和突变型细胞在25℃下光合自养生长速率相当。然而,在40℃下生长时,突变型细胞生长较慢且叶绿素含量低于野生型细胞。在任一温度下生长的细胞中,不含PsaI的膜与野生型膜相比,NADP+光还原速率略有下降。psaI失活导致光合膜中PsaL水平降低80%,在纯化的光系统I制剂中PsaL完全缺失,但对其他光系统I亚基的积累影响很小。用非离子型去污剂溶解后,野生型可获得光系统I三聚体,而不含PsaI的膜则不能。不含PsaI的光系统I单体不含可检测水平的PsaL。因此,PsaL和PsaI之间的结构相互作用可能稳定PsaL与光系统I核心的结合。野生型和不含PsaI的膜中的PsaL对离液剂去除具有同等抗性。然而,不含PsaI菌株中的PsaL对蛋白水解的敏感性增加。根据这些数据,我们得出结论,PsaI在辅助光系统I复合物中PsaL的正常结构组织方面具有关键作用,PsaI的缺失改变了PsaL的组织,导致光系统I功能出现微小但具有生理意义的缺陷。

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