您的位置: 专家智库 > >

国家林业局948项目(2004-4-58)

作品数:1 被引量:16H指数:1
相关作者:彭镇华刘成刘颖丽高志民更多>>
相关机构:中国林业科学研究院国际竹藤网络中心中国科学院植物研究所更多>>
发文基金:引进国际先进农业科技计划国家林业局重点科研项目更多>>
相关领域:生物学农业科学更多>>

文献类型

  • 1篇中文期刊文章

领域

  • 1篇生物学
  • 1篇农业科学

主题

  • 1篇原核表达
  • 1篇特异性表达
  • 1篇组织特异性
  • 1篇组织特异性表...
  • 1篇毛竹
  • 1篇CAB

机构

  • 1篇中国科学院植...
  • 1篇中国林业科学...
  • 1篇国际竹藤网络...

作者

  • 1篇高志民
  • 1篇刘颖丽
  • 1篇刘成
  • 1篇彭镇华

传媒

  • 1篇林业科学

年份

  • 1篇2009
1 条 记 录,以下是 1-1
排序方式:
毛竹捕光叶绿素a/b结合蛋白基因cab-PhE1的克隆与表达分析被引量:16
2009年
The light harvesting chlorophyll a/b-binding protein is one of key proteins in the transformation from light energy to chemical energy. An open reading frame coding precursor protein of cab gene was cloned from the first strand of bamboo cDNA through RT-PCR methods,and named as cab-PhE1 (cab gene 1 from Phyllostachys edulis EF207229). The sequence analysis showed that the deduced polypeptide was highly homologous to some other CAB proteins from monocotyledon,and the gene belonged to lhcb2 family. Tissue specific expression showed that cab-PhE1 expressed higher in leaf than sheath and stem. The prokaryotic expression vector of cab-PhE1 gene encoding the mature protein was constructed by subcloning the fragment into pET-23 a and was expressed in Escherichia coli induced by IPTG. The molecular weight of the induced protein was about 28 ku,approximate to that of the mature protein. This work is a key to the further research on in vitro reconstitution of light-harvesting Chl a/b complexes.
高志民刘成刘颖丽彭镇华
关键词:毛竹组织特异性表达原核表达
共1页<1>
聚类工具0