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集胞藻PCC 7942中psbD基因家族的光调节表达:蓝细菌中重复的psbD基因作用的证据

Light-regulated expression of the psbD gene family in Synechococcus sp. strain PCC 7942: evidence for the role of duplicated psbD genes in cyanobacteria.

作者信息

Bustos S A, Golden S S

机构信息

Department of Biology, Texas A & M University, College Station 77843.

出版信息

Mol Gen Genet. 1992 Mar;232(2):221-30. doi: 10.1007/BF00280000.

Abstract

The genome of the cyanobacterium Synechococcus sp. strain PCC 7942 contains two psbD genes encoding the D2 protein of the photosystem II reaction center: psbDI, which is cotranscribed as a discistronic message with psbC (the gene encoding CP43, a chlorophyll-a binding protein), and psbDII, which is monocistronic. Northern blot analysis of psbD transcripts showed that the two genes responded differently when wild-type cells were shifted from moderate to high light intensity. Whereas psbDII transcripts increased 500% relative to unshifted control cells, psbDI-psbC transcripts remained unchanged. The beta-galactosidase activities expressed from translational fusions between the psbD genes and the Escherichia coli lacZ reporter gene displayed responses similar to those seen in the RNA. D2 protein levels in thylakoid membranes from wild-type cells increased to 250% of those of the unshifted control cells 12 h after a shift to high light intensities. In contrast, in a mutant strain (AMC016) that carries an inactive psbDII gene, D2 levels decreased by 50% under identical conditions. These results suggested that induction of psbDII gene expression by light can serve as a supplementary system for maintaining a functional photosystem II reaction center at high light intensity. This hypothesis was corroborated by mixed-culture experiments, in which AMC016 cells competed poorly with wild-type cells at high light intensity. These data suggest for the first time that differential expression of members of a cyanobacterial gene family serves to maintain a functional PSII reaction center under diverse environmental conditions.

摘要

集胞藻属蓝细菌PCC 7942菌株的基因组包含两个编码光系统II反应中心D2蛋白的psbD基因:psbDI,它与psbC(编码CP43,一种叶绿素a结合蛋白的基因)作为双顺反子信息共转录;以及psbDII,它是单顺反子。对psbD转录本的Northern印迹分析表明,当野生型细胞从中等光照强度转移到高光强度时,这两个基因的反应不同。相对于未转移的对照细胞,psbDII转录本增加了500%,而psbDI - psbC转录本保持不变。从psbD基因与大肠杆菌lacZ报告基因之间的翻译融合表达的β-半乳糖苷酶活性显示出与RNA中相似的反应。转移到高光强度12小时后,野生型细胞类囊体膜中的D2蛋白水平增加到未转移对照细胞的250%。相反,在携带无活性psbDII基因的突变菌株(AMC016)中,在相同条件下D2水平下降了50%。这些结果表明,光诱导psbDII基因表达可作为在高光强度下维持功能性光系统II反应中心的补充系统。混合培养实验证实了这一假设,在该实验中,AMC016细胞在高光强度下与野生型细胞竞争能力较差。这些数据首次表明,蓝细菌基因家族成员的差异表达有助于在不同环境条件下维持功能性PSII反应中心。

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