首页> 外文期刊>园艺学报:英文版 >Molecular Cloning and Expression Analysis of the ζ-Carotene Desaturase Gene in Chinese kale(Brassica oleracea var.alboglabra Bailey)
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Molecular Cloning and Expression Analysis of the ζ-Carotene Desaturase Gene in Chinese kale(Brassica oleracea var.alboglabra Bailey)

机译:芥蓝中β-胡萝卜素去饱和酶基因的分子克隆和表达分析

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摘要

ζ-Carotene desaturase(ZDS)is an important enzyme in carotenoid biosynthesis.Here,the Brassica oleracea var.alboglabra ZDS(Boa ZDS)gene was cloned from Chinese kale via reverse transcription-polymerase chain reaction(RT-PCR)and deposited in Gen Bank(accession number KY662297).The Boa ZDS gene contains an open reading frame of 1 686 bp that encodes a 561-amino acid protein.Sequence analysis indicates that the ZDS protein is apparently conserved during plant evolution and is most closely related to B.oleracea var.capitata and B.rapa.The promoter sequence of the Boa ZDS gene was predicted to harbor several cis-acting elements that are related to light and phytohormone responses.Semiquantitative RT-PCR analysis showed that Boa ZDS expression varied among different developmental stages and organs.Relative ZDS expression remained stable during germination and seedling stages and rapidly increased at the mature leaf stage.The leaves showed the highest ZDS expression levels compared to the other organs.ZDS expression decreased in all flower tissues during blooming.The fused protein of Boa ZDS was obtained by prokaryotic expression.Heterologous expression of Boa ZDS in Escherichia coli confirmed that Boa ZDS encodes a functionalζ-carotene desaturase that increases β-carotene accumulation in E.coli cells harboring a β-carotene-producing plasmid.The findings of the present study provide a molecular basis for the elucidation of ZDS gene function in Chinese kale.
机译:ζ-胡萝卜素去饱和酶(ZDS)是类胡萝卜素生物合成中的一种重要酶。在此,通过逆转录-聚合酶链反应(RT-PCR)从芥蓝中克隆了甘蓝型油菜(Brassica oleracea var.alboglabra)ZDS(Boa ZDS)基因,并将其存放在Gen银行(登录号KY662297).Boa ZDS基因包含一个1 686 bp的开放阅读框,编码561个氨基酸的蛋白质。序列分析表明ZDS蛋白在植物进化过程中显然是保守的,并且与B密切相关。预测Boa ZDS基因的启动子序列中含有几个与光和植物激素反应有关的顺式作用元件。半定量RT-PCR分析表明Boa ZDS表达在不同发育阶段有所不同ZDS的相对表达在发芽和幼苗期保持稳定,并在成熟叶期迅速增加。与其他植物相比,叶片的ZDS表达水平最高开花时所有花组织中ZDS的表达均下降,通过原核表达获得Boa ZDS的融合蛋白,Boa ZDS在大肠杆菌中的异源表达证实Boa ZDS编码功能性ζ-胡萝卜素去饱和酶,增加了β-胡萝卜素的积累E.coli细胞带有一个生成β-胡萝卜素的质粒。本研究的发现为阐明芥蓝中ZDS基因的功能提供了分子基础。

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  • 来源
    《园艺学报:英文版》 |2018年第003期|P.94-102|共9页
  • 作者单位

    College of Horticulture,Sichuan Agricultural University;

    Department of Horticulture,Zhejiang University;

    College of Horticulture,Sichuan Agricultural University;

    Department of Horticulture,Zhejiang University;

    College of Horticulture,Sichuan Agricultural University;

    Department of Horticulture,Zhejiang University;

    College of Horticulture,Sichuan Agricultural University;

    Department of Horticulture,Zhejiang University;

    College of Horticulture,Sichuan Agricultural University;

    Department of Horticulture,Zhejiang University;

    College of Horticulture,Sichuan Agricultural University;

    Department of Horticulture,Zhejiang University;

    College of Horticulture,Sichuan Agricultural University;

    Department of Horticulture,Zhejiang University;

    College of Horticulture,Sichuan Agricultural University;

    Department of Horticulture,Zhejiang University;

    College of Horticulture,Sichuan Agricultural University;

    Department of Horticulture,Zhejiang University;

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  • 原文格式 PDF
  • 正文语种 CHI
  • 中图分类 植物基因工程;
  • 关键词

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