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Complementary DNA cloning and characterization of ferredoxin localized in bundle-sheath cells of maize leaves

机译:玉米叶片束鞘细胞中铁氧还蛋白的互补DNA克隆和鉴定

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摘要

In maize (Zea mays L.) two leaf-specific ferredoxin (Fd) isoproteins, Fd I and Fd II, are distributed differentially in mesophyll and bundle-sheath cells. A novel cDNA encoding the precursor of Fd II (pFD2) was isolated by heterologous hybridization using a cDNA for Fd I (pFD1) as a probe. The assignment of the cDNAs to the Fds was verified by capillary liquid-chromatography/electrospray ionization-mass spectrometry. RNA-blot analysis demonstrated that transcripts for Fd I and Fd II accumulated specifically in mesophyll and bundle-sheath cells, respectively. The mature regions of pFD1 and pFD2 were expressed in Escherichia coli as functional Fds. Fd I and Fd II had similar redox potentials of -423 and -406 mV, respectively, but the K(m) value of Fd-NADP superior + reductase for Fd II was about 3-fold larger than that for Fd I. Asparagine at position 65 of Fd II is a unique residue compared with Fd I and other Fds from various plants, which have aspartic acid or glutamic acid at the corresponding position as an electrostatic interaction site with Fd-NADP superior + reductase. Substitution of asparagine-65 with aspartic acid increased the affinity of Fd II with Fd-NADP superior + reductase to a level comparable to that of Fd I. These structural and functional differences of Fd I and Fd II may be related to their cell-specific expression in the leaves of a C inferior 4 plant.
机译:在玉米(Zea mays L.)中,两种叶特异性铁氧还蛋白(Fd)同蛋白Fd I和Fd II在叶肉和束鞘细胞中差异分布。使用Fd I的cDNA(pFD1)作为探针,通过异源杂交分离了编码Fd II的前体的新cDNA(pFD2)。通过毛细管液相色谱/电喷雾电离质谱法验证了将cDNA分配给Fds。 RNA印迹分析表明,Fd I和Fd II的转录本分别在叶肉和束鞘细胞中特异性积累。 pFD1和pFD2的成熟区域在大肠杆菌中以功能性Fds的形式表达。 Fd I和Fd II的氧化还原电位分别相似,分别为-423和-406 mV,但Fd II的Fd-NADP上等+还原酶的K(m)值比Fd I的K(m)约大3倍。与Fd I和其他植物的Fd相比,Fd II的65位是一个独特的残基,后者在相应位置具有天冬氨酸或谷氨酸作为与Fd-NADP上位+还原酶的静电相互作用位点。用天冬氨酸替代天冬酰胺65可使Fd II与Fd-NADP上清+还原酶的亲和力提高到与Fd I相当的水平。FdI和Fd II的这些结构和功能差异可能与其细胞特异性有关在劣质C 4植物的叶子中表达。

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