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Functional Analysis of the Nitrogenase-Like Protochlorophyllide Reductase Encoded in Chloroplast Genome Using Cyanobacterium Leptolyngbya Boryana

机译:叶绿体蓝单胞菌Boryana对叶绿体基因组中编码的氮酶类似的原绿叶素还原酶的功能分析

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Dark-operative protochlorophyllide (Pchlide) reductase (DPOR) is a nitrogenase-like enzyme consisting of two separable components, L-protein (a ChlL dimer) and NB-protein (a ChlN-ChlB heterotetramer), which are structural counterparts of Fe protein and MoFe protein of nitrogenase, respectively. In contrast to the limited distribution of nitrogenase only among prokaryotes, DPOR is distributed among not only photosynthetic prokaryotes but also eukaryotic phototrophs such as green algae, moss, ferns and gymnosperms. While prokaryotic DPORs have been characterized, there has very little study on eukaryotic DPOR functioning in the chloroplast The three structural genes of DPOR, chlL, chlN and MB, are encoded by the chloroplast DNA. Recently we have established an in-vivo complementation system using mutants lacking DPOR genes of the cyanobacterium Leptolyngbya boryana to examine whether DPOR genes are functional. We applied this system to evaluate the probable DPOR genes encoded by the chloroplast DNAs from the moss Physcomitrella patens and black pine Pinus thunbergii. We discuss the functional operation of DPOR in the chloroplasts of these photosynthetic eukaryotes.
机译:暗部操作的原叶绿素(Pchlide)还原酶(DPOR)是一种类似N的酶,由两个可分离的成分L蛋白(ChlL二聚体)和NB蛋白(ChlN-ChlB异四聚体)组成,它们是Fe蛋白的结构对应物和固氮酶的MoFe蛋白。与仅在原核生物中有限的固氮酶分布相反,DPOR不仅分布在光合作用的原核生物中,而且还分布在真核生物营养体中,例如绿藻,苔藓,蕨类和裸子植物。虽然已经鉴定了原核DPOR,但是对真核DPOR在叶绿体中的功能的研究很少。叶绿体DNA编码DPOR的三个结构基因,即chlL,chlN和MB。最近,我们已经建立了一种体内互补系统,该系统利用缺少蓝细菌钩端螺旋体的DPOR基因的突变体来检查DPOR基因是否具有功能。我们应用该系统评估了苔藓小立碗藓和黑松黑松的叶绿体DNA编码的可能的DPOR基因。我们讨论了DPOR在这些光合真核生物叶绿体中的功能操作。

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