IOCAS-IR  > 实验海洋生物学重点实验室
Cloning and characterization of beta-carotene ketolase gene promoter in Haematococcus pluvialis
Meng, CX; Teng, CY; Jiang, P; Qin, S; Tseng, CK
2005-04-01
发表期刊ACTA BIOCHIMICA ET BIOPHYSICA SINICA
ISSN1672-9145
卷号37期号:4页码:270-275
文章类型Article
摘要The unicellular green alga Haematococcus pluvialis accumulates a highly valuable ketocarotenoid, astaxanthin, under various environmental stresses. beta-carotene ketolase (BKT) plays a key role in astaxanthin biosynthesis in H. pluvialis. In this paper, an approximate 700 bp 5'-flanking region of the bkt gene containing a putative promoter was cloned through walking upstream. The results of the sequence analysis showed that this bkt 5'-flanking region might have cis-acting elements such as sterol regulatory element (SRE-1)-like motifs, the C-repeat/dehydration responsive element (DRE) and al-3 proximal element (APE)-like motifs, except for typical TATA and CCAAT boxes. The results of the P-galactosidase assay and the transient expression of lacZ driven by a series of sequential deletions revealed that a minimal promoter-like region might exist from -630 to -408 bp, and the highest promoter activity was observed to span the positions from -630 to -308 bp. The results of the site-directed mutagenesis of a C-repeat/DRE and two APE-like motifs in a promoter-like region (-630 to -308 bp) suggested that two APE-like motifs might be essential for transcriptional control of the bkt gene.; The unicellular green alga Haematococcus pluvialis accumulates a highly valuable ketocarotenoid, astaxanthin, under various environmental stresses. beta-carotene ketolase (BKT) plays a key role in astaxanthin biosynthesis in H. pluvialis. In this paper, an approximate 700 bp 5'-flanking region of the bkt gene containing a putative promoter was cloned through walking upstream. The results of the sequence analysis showed that this bkt 5'-flanking region might have cis-acting elements such as sterol regulatory element (SRE-1)-like motifs, the C-repeat/dehydration responsive element (DRE) and al-3 proximal element (APE)-like motifs, except for typical TATA and CCAAT boxes. The results of the P-galactosidase assay and the transient expression of lacZ driven by a series of sequential deletions revealed that a minimal promoter-like region might exist from -630 to -408 bp, and the highest promoter activity was observed to span the positions from -630 to -308 bp. The results of the site-directed mutagenesis of a C-repeat/DRE and two APE-like motifs in a promoter-like region (-630 to -308 bp) suggested that two APE-like motifs might be essential for transcriptional control of the bkt gene.
关键词Haematococcus Pluvialis Astaxanthin Beta-carotene Ketolase Gene (Bkt) Cis-acting Element Promoter
学科领域Biochemistry & Molecular Biology ; Biophysics
DOI10.1111/j.1745-7270.2005.00033.x
URL查看原文
收录类别SCI
语种英语
WOS记录号WOS:000228545300009
引用统计
被引频次:28[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/337002/3112
专题实验海洋生物学重点实验室
作者单位1.Chinese Acad Sci, Inst Oceanol, Qingdao 266071, Peoples R China
2.Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
推荐引用方式
GB/T 7714
Meng, CX,Teng, CY,Jiang, P,et al. Cloning and characterization of beta-carotene ketolase gene promoter in Haematococcus pluvialis[J]. ACTA BIOCHIMICA ET BIOPHYSICA SINICA,2005,37(4):270-275.
APA Meng, CX,Teng, CY,Jiang, P,Qin, S,&Tseng, CK.(2005).Cloning and characterization of beta-carotene ketolase gene promoter in Haematococcus pluvialis.ACTA BIOCHIMICA ET BIOPHYSICA SINICA,37(4),270-275.
MLA Meng, CX,et al."Cloning and characterization of beta-carotene ketolase gene promoter in Haematococcus pluvialis".ACTA BIOCHIMICA ET BIOPHYSICA SINICA 37.4(2005):270-275.
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
meng-Cloning and cha(611KB) 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
[Meng, CX]的文章
[Teng, CY]的文章
[Jiang, P]的文章
百度学术
百度学术中相似的文章
[Meng, CX]的文章
[Teng, CY]的文章
[Jiang, P]的文章
必应学术
必应学术中相似的文章
[Meng, CX]的文章
[Teng, CY]的文章
[Jiang, P]的文章
相关权益政策
暂无数据
收藏/分享
文件名: meng-Cloning and characterization of beta.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。