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来自巴氏杜氏藻的香叶基香叶基二磷酸合酶编码基因的表征与功能鉴定

Characterization and Functional Identification of a Gene Encoding Geranylgeranyl Diphosphate Synthase from Dunaliella bardawil.

作者信息

Liang Ming-Hua, Liang Ying-Jie, Jin Hong-Hao, Jiang Jian-Guo

机构信息

College of Food Science and Engineering, South China University of Technology , Guangzhou 510640, China.

School of Biological Science & Engineering, South China University of Technology , Guangzhou 510006, China.

出版信息

J Agric Food Chem. 2015 Sep 9;63(35):7805-12. doi: 10.1021/acs.jafc.5b02732. Epub 2015 Aug 25.

Abstract

Geranylgeranyl diphosphate synthase (GGPS) catalyzes the biosynthesis of geranylgeranyl diphosphate, a key precursor for carotenoid biosynthesis. In this study, a full-length cDNA encoding GGPS from Dunaliella bardawil (DbGGPS) was isolated by rapid amplification of cDNA ends (RACE) for the first time. The full-length cDNA of DbGGPS was 1814 bp, containing a 1074 bp ORF encoding 357 amino acids with a calculated mass of 38.88 kDa. Analysis of DbGGPS genomic DNA revealed that it contained 10 exons and 9 introns. It was predicted that DbGGPS possessed a 48 amino acid transit peptide at its N terminus. Bioinformatic analysis revealed that DbGGPS was a member of a group of polyprenyltransferases with five conserved domains and two highly conserved aspartate-rich motifs. Using heterologous expression, carotenoid complementation assay, and gene deletion analysis, it was shown that the coding region of DbGGPS encodes a functional GGPS. This provides new gene sources for carotenoid genetic engineering.

摘要

香叶基香叶基二磷酸合酶(GGPS)催化香叶基香叶基二磷酸的生物合成,香叶基香叶基二磷酸是类胡萝卜素生物合成的关键前体。在本研究中,首次通过cDNA末端快速扩增(RACE)从巴氏杜氏藻(DbGGPS)中分离出编码GGPS的全长cDNA。DbGGPS的全长cDNA为1814 bp,包含一个1074 bp的开放阅读框,编码357个氨基酸,计算分子量为38.88 kDa。对DbGGPS基因组DNA的分析表明,它包含10个外显子和9个内含子。预测DbGGPS在其N端具有一个48个氨基酸的转运肽。生物信息学分析表明,DbGGPS是一组聚异戊二烯转移酶的成员,具有五个保守结构域和两个高度保守的富含天冬氨酸的基序。通过异源表达、类胡萝卜素互补分析和基因缺失分析表明,DbGGPS的编码区编码一种功能性GGPS。这为类胡萝卜素基因工程提供了新的基因来源。

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