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烟草NtGGPPS4基因的克隆和功能初步分析

李锋 孟利军 史艳梅 郑庆霞 刘萍萍 魏春阳 王燃 杨军 罗朝鹏

烟草科技2017,Vol.50Issue(1):1-5,5.
烟草科技2017,Vol.50Issue(1):1-5,5.DOI:10.16135/j.issn1002-0861.2016.0373

烟草NtGGPPS4基因的克隆和功能初步分析

Cloning and functional analysis of NtGGPPS4 from Nicotiana tabacum

李锋 1孟利军 2史艳梅 3郑庆霞 1刘萍萍 1魏春阳 4王燃 1杨军 1罗朝鹏1

作者信息

  • 1. 中国烟草总公司郑州烟草研究院,郑州高新技术产业开发区枫杨街2号 450001
  • 2. 河南农业大学食品科学技术学院,郑州市文化路95号 450002
  • 3. 河南中医药大学科技处,郑州市金水路1号 450008
  • 4. 中国烟草总公司职工进修学院,郑州市鑫苑路7号 450008
  • 折叠

摘要

Abstract

To clarify the function of geranylgeranyl pyrophosphate synthase gene (NtGGPPS4) in tobacco, the coding sequence of NtGGPPS4 gene was cloned from Nicotiana tabacum. The over-expression vector pCAMBIA1300-NtGGPPS4 was constructed and transferred into Nicotiana tabacum by Agrobacterium tumefaciens mediated method. The contents of α- and β-cembrenediol and plastid pigments in transgenic tobacco plants were measured. The results showed that four transgenic tobacco plants which showed high levels of NtGGPPS4 were obtained. Comparing with the control, the contents of α- and β-cembrenediol, neoxanthin, violaxanthin, lutein, chlorophyll a, chlorophyll b and β-carotene increased significantly in transgenic plants. It indicated that NtGGPPS4 was involved in the biosynthesis of α- and β-cembrenediol and carotenoids in tobacco.

关键词

烟草/牻牛儿基牻牛儿基焦磷酸合成酶基因/超量表达/功能分析

Key words

Nicotiana tabacum/Geranylgeranyl pyrophosphate synthase gene/Over-expression/Functional analysis

分类

轻工纺织

引用本文复制引用

李锋,孟利军,史艳梅,郑庆霞,刘萍萍,魏春阳,王燃,杨军,罗朝鹏..烟草NtGGPPS4基因的克隆和功能初步分析[J].烟草科技,2017,50(1):1-5,5.

基金项目

郑州烟草研究院科技项目“烟草萜类化合物合成关键基因NtGGPPS功能分析和调控机制研究”(902012CZ340)。 ()

烟草科技

OA北大核心CSCDCSTPCD

1002-0861

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