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描述集胞藻 PCC 6803 的 psbK 基因座在光系统 II 功能方面的特征。

Characterization of the psbK locus of Synechocystis sp. PCC 6803 in terms of Photosystem II function.

机构信息

AFRC Photosynthesis Research Group, Wolfson Laboratories, Biochemistry Department, Imperial College of Science, Technology & Medicine, SW7 2AY, London, UK.

出版信息

Photosynth Res. 1993 Jan;38(3):369-77. doi: 10.1007/BF00046763.

Abstract

The psbK gene encodes a small protein of Photosystem II. The gene has previously been cloned and sequenced in Synechocystis sp. PCC 6803. Our new results, presented here, confirm the conclusions of Ikeuchi et al. Based on Northern hybridization and primer extension analyses, we show that psbK is transcribed as a monocistronic message in this cyanobacterium. Analysis of DNA sequence immediately upstream of the transcription start site revealed an E. coli-like-10 consensus sequence. A deletion mutant was constructed where the psbK gene was replaced by a kanamycin resistant cartridge. In situ complementation experiments, as well as Southern and Northern hybridization analyses, confirmed that the mutant strain contains a lesion in psbK. The psbK-less mutant could grow photoautotrophically as well as photoheterotrophically both in liquid culture and on agar plates. The rate of growth was slightly less compared with the wild-type as clearly observed by in situ complementation experiments. Although the mutant showed correspondingly lower rates of electron transport, thermoluminescence, oxygen flash yield and chlorophyll a fluorescence measurements did not detect any significant modification of the reactions of PS II. Moreover, the mutant was no more susceptible to excess light than the wild-type. It is, therefore, concluded that the product of the psbK gene is not crucial for PS II activity and possibly plays some other role in the metabolism of Synechocystis.

摘要

psbK 基因编码光合系统 II 的一个小蛋白。该基因已在集胞藻 PCC 6803 中被克隆和测序。我们在此呈现的新结果证实了 Ikeuchi 等人的结论。通过 Northern 杂交和引物延伸分析,我们表明 psbK 在这种蓝藻中作为单顺反子转录。对转录起始位点上游的 DNA 序列进行分析,揭示了一个类似于大肠杆菌的-10 共识序列。构建了一个缺失突变体,其中 psbK 基因被卡那霉素抗性盒取代。原位互补实验以及 Southern 和 Northern 杂交分析证实,突变株在 psbK 中存在缺陷。psbK 缺失突变体能在液体培养和琼脂平板上进行光自养和光异养生长。与野生型相比,通过原位互补实验清楚地观察到生长速度略有降低。尽管突变体的电子传递、热致发光、氧闪光产额和叶绿素 a 荧光测量的速率相应较低,但 PS II 的反应没有检测到任何明显的修饰。此外,突变体对过量光的敏感性并不高于野生型。因此,可以得出结论,psbK 基因的产物对于 PS II 活性不是至关重要的,并且可能在集胞藻的代谢中发挥其他作用。

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