IOCAS-IR  > 实验海洋生物学重点实验室
Serine/Threonine Protein Kinase SpkG Is a Candidate for High Salt Resistance in the Unicellular Cyanobacterium Synechocystis sp PCC 6803
Liang, Chengwei1,2; Zhang, Xiaowen2,3; Chi, Xiaoyuan2; Guan, Xiangyu4; Li, Youxun2; Qin, Song2; Shao, Hong Bo5
2011-05-26
发表期刊PLOS ONE
ISSN1932-6203
卷号6期号:5页码:e18718
文章类型Article
摘要Background: Seven serine/threonine kinase genes have been predicted in unicellular cyanobacterium Synechocystis sp. PCC6803. SpkA and SpkB were shown to be required for cell motility and SpkE has no kinase activity. There is no report whether the other four STKs are involved in stress-mediated signaling in Synechocystis PCC6803.; Background: Seven serine/threonine kinase genes have been predicted in unicellular cyanobacterium Synechocystis sp. PCC6803. SpkA and SpkB were shown to be required for cell motility and SpkE has no kinase activity. There is no report whether the other four STKs are involved in stress-mediated signaling in Synechocystis PCC6803. Methodology/Principal Findings: In this paper, we examined differential expression of the other four serine/threonine kinases, SpkC, SpkD, SpkF and SpkG, at seven different stress conditions. The transcriptional level was up-regulated of spkG and down-regulated of spkC under high salt stress condition. Two spk deletion mutants, Delta spkC and Delta spkG, were constructed and their growth characteristic were examined compared to the wild strain. The wild strain and Delta spkC mutant were not affected under high salt stress conditions. In contrast, growth of spkG mutant was completely impaired. To further confirm the function of spkG, we also examined the effect of mutation of spkG on the expression of salt stress-inducible genes. We compared genome-wide patterns of transcription between wild-type Synechocystis sp. PCC6803 and cells with a mutation in the SpkG with DNA microarray analysis. Conclusion: In this study, we first study the spkG gene as sensor of high salt signal. We consider that SpkG play essential roles in Synechocystis sp. for sensing the high salt signal directly, rather than mediating signals among other kinases. Our microarray experiment may help select relatively significant genes for further research on mechanisms of signal transduction of Synechocystis sp. PCC6803 under high salt stress.
学科领域Life Sciences & Biomedicine - Other Topics
DOI10.1371/journal.pone.0018718
URL查看原文
收录类别SCI
语种英语
WOS记录号WOS:000291052200008
引用统计
被引频次:30[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.qdio.ac.cn/handle/337002/11941
专题实验海洋生物学重点实验室
作者单位1.Qingdao Univ Sci & Technol, Qingdao, Peoples R China
2.Chinese Acad Sci, Inst Oceanol, Qingdao, Peoples R China
3.Chinese Acad Fishery Sci, Yellow Sea Fisheries Res Inst, Qingdao, Peoples R China
4.Ocean Univ China, Qingdao, Peoples R China
5.Chinese Acad Sci, Yantai Inst Coastal Zone Res, Yantai, Peoples R China
第一作者单位中国科学院海洋研究所
推荐引用方式
GB/T 7714
Liang, Chengwei,Zhang, Xiaowen,Chi, Xiaoyuan,et al. Serine/Threonine Protein Kinase SpkG Is a Candidate for High Salt Resistance in the Unicellular Cyanobacterium Synechocystis sp PCC 6803[J]. PLOS ONE,2011,6(5):e18718.
APA Liang, Chengwei.,Zhang, Xiaowen.,Chi, Xiaoyuan.,Guan, Xiangyu.,Li, Youxun.,...&Shao, Hong Bo.(2011).Serine/Threonine Protein Kinase SpkG Is a Candidate for High Salt Resistance in the Unicellular Cyanobacterium Synechocystis sp PCC 6803.PLOS ONE,6(5),e18718.
MLA Liang, Chengwei,et al."Serine/Threonine Protein Kinase SpkG Is a Candidate for High Salt Resistance in the Unicellular Cyanobacterium Synechocystis sp PCC 6803".PLOS ONE 6.5(2011):e18718.
条目包含的文件
文件名称/大小 文献类型 版本类型 开放类型 使用许可
Serine Threonine Pro(445KB) 限制开放--浏览
个性服务
推荐该条目
保存到收藏夹
查看访问统计
导出为Endnote文件
谷歌学术
谷歌学术中相似的文章
[Liang, Chengwei]的文章
[Zhang, Xiaowen]的文章
[Chi, Xiaoyuan]的文章
百度学术
百度学术中相似的文章
[Liang, Chengwei]的文章
[Zhang, Xiaowen]的文章
[Chi, Xiaoyuan]的文章
必应学术
必应学术中相似的文章
[Liang, Chengwei]的文章
[Zhang, Xiaowen]的文章
[Chi, Xiaoyuan]的文章
相关权益政策
暂无数据
收藏/分享
文件名: Serine Threonine Protein Kinase SpkG Is a Candidate for High Salt Resistance in the Unicellular Cyanobacterium Synechocystis sp PCC 6803.pdf
格式: Adobe PDF
此文件暂不支持浏览
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。