Enhanced green fluorescent protein (egfp) gene expression in Tetraselmis subcordiformis chloroplast with endogenous regulators
Cui, YL; Zhao, JL; Hou, SC; Qin, S; Qin, S (reprint author), Chinese Acad Sci, Yantai Inst Coastal Zone Res, Key Lab Coastal Biol & Biol Resource Utilizat, Chunhui Rd 17, Yantai 264003, Shandong, Peoples R China. yulincui@yic.ac.cn; sqin@yic.ac.cn
发表期刊WORLD JOURNAL OF MICROBIOLOGY & BIOTECHNOLOGY
ISSN0959-3993
2016-05-01
卷号32期号:5
关键词Tetraselmis Subcordiformis Chloroplast Promoters Bombardment
DOI10.1007/s11274-016-2039-y
产权排序[Cui, Yulin; Zhao, Jialin; Qin, Song] Chinese Acad Sci, Yantai Inst Coastal Zone Res, Key Lab Coastal Biol & Biol Resource Utilizat, Chunhui Rd 17, Yantai 264003, Shandong, Peoples R China; [Zhao, Jialin] Univ Chinese Acad Sci, Yuquan Rd 19, Beijing 100049, Peoples R China; [Hou, Shichang] Yantai Univ, Coll Life Sci, Qingquan Rd 30, Yantai 264005, Shandong, Peoples R China
作者部门海岸带生物学与生物资源利用所重点实验室
英文摘要On the basis of fundamental genetic transformation technologies, the goal of this study was to optimize Tetraselmis subcordiformis chloroplast transformation through the use of endogenous regulators. The genes rrn16S, rbcL, psbA, and psbC are commonly highly expressed in chloroplasts, and the regulators of these genes are often used in chloroplast transformation. For lack of a known chloroplast genome sequence, the genome-walking method was used here to obtain full sequences of T. subcordiformis endogenous regulators. The resulting regulators, including three promoters, two terminators, and a ribosome combination sequence, were inserted into the previously constructed plasmid pPSC-R, with the egfp gene included as a reporter gene, and five chloroplast expression vectors prepared. These vectors were successfully transformed into T. subcordiformis by particle bombardment and the efficiency of each vector tested by assessing EGFP fluorescence via microscopy. The results showed that these vectors exhibited higher efficiency than the former vector pPSC-G carrying exogenous regulators, and the vector pRFA with Prrn, psbA-5'RE, and TpsbA showed the highest efficiency. This research provides a set of effective endogenous regulators for T. subcordiformis and will facilitate future fundamental studies of this alga.
文章类型Article
资助机构National Natural Science Foundation of China(41406192 ; Science Foundation of the Chinese Academy of Sciences(XDA1102040300) ; 41176144 ; 41376139)
收录类别SCI
语种英语
关键词[WOS]ALGA PLATYMONAS-SUBCORDIFORMIS ; PLASTID TRANSFORMATION ; VECTOR ; CONSTRUCTION ; SEQUENCES ; ELEMENTS ; TOBACCO ; OPERON
研究领域[WOS]Biotechnology & Applied Microbiology
WOS记录号WOS:000375089400012
引用统计
被引频次:7[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.yic.ac.cn/handle/133337/17058
专题海岸带生物学与生物资源利用重点实验室_海岸带生物学与生物资源保护实验室
通讯作者Qin, S (reprint author), Chinese Acad Sci, Yantai Inst Coastal Zone Res, Key Lab Coastal Biol & Biol Resource Utilizat, Chunhui Rd 17, Yantai 264003, Shandong, Peoples R China. yulincui@yic.ac.cn; sqin@yic.ac.cn
作者单位1.Chinese Acad Sci, Yantai Inst Coastal Zone Res, Key Lab Coastal Biol & Biol Resource Utilizat
2.Univ Chinese Acad Sci
3.Yantai Univ, Coll Life Sci
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GB/T 7714
Cui, YL,Zhao, JL,Hou, SC,et al. Enhanced green fluorescent protein (egfp) gene expression in Tetraselmis subcordiformis chloroplast with endogenous regulators[J]. WORLD JOURNAL OF MICROBIOLOGY & BIOTECHNOLOGY,2016,32(5).
APA Cui, YL,Zhao, JL,Hou, SC,Qin, S,Qin, S ,&sqin@yic.ac.cn.(2016).Enhanced green fluorescent protein (egfp) gene expression in Tetraselmis subcordiformis chloroplast with endogenous regulators.WORLD JOURNAL OF MICROBIOLOGY & BIOTECHNOLOGY,32(5).
MLA Cui, YL,et al."Enhanced green fluorescent protein (egfp) gene expression in Tetraselmis subcordiformis chloroplast with endogenous regulators".WORLD JOURNAL OF MICROBIOLOGY & BIOTECHNOLOGY 32.5(2016).
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