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豌豆线粒体核苷二磷酸激酶的克隆与特性分析

Cloning and characterisation of a pea mitochondrial NDPK.

作者信息

Escobar Galvis M L, Håkansson G, Alexciev K, Knorpp C

机构信息

Plant Cell Biology, Lund University, Sweden.

出版信息

Biochimie. 1999 Dec;81(12):1089-96. doi: 10.1016/s0300-9084(99)00353-3.

Abstract

Here we report the cloning of a cDNA encoding the first nucleoside diphosphate kinase (NDPK) isolated from plant mitochondria. Amplification of a 317 nt product was performed by PCR, using oligonucleotide primers based on partial amino acid sequences of the pea mitochondria NDPK and other NDPK isoforms. By screening of a pea cDNA library with this PCR product, a full length clone was obtained. Northern analysis revealed the presence of a 1.1 kb single transcript, with high expression in young leaves and reproductive tissues. The clone encodes a precursor protein of 232 amino acids (26 kDa), including an N-terminal extension of 80 amino acids (9 kDa). Analysis of the deduced amino acid sequence confirmed its identity with the sequences obtained from the purified mature pea mitochondrial NDPK. In vitro import experiments carried out in isolated pea mitochondria showed targeting and processing of the 27 kDa precursor into a 16.5 kDa mature form. Phylogenetic analysis of some vertebrate and plant isoforms of NDPK showed that the pea mtNDPK groups together with the NDPK3 isoform from A. thaliana and the chloroplastic NDPK III from spinach. We suggest that it is possible to design a novel classification of the different NDPK isoforms according to their subcellular localisation and origin.

摘要

在此,我们报道了从植物线粒体中分离出的首个核苷二磷酸激酶(NDPK)编码cDNA的克隆。利用基于豌豆线粒体NDPK和其他NDPK同工型部分氨基酸序列的寡核苷酸引物,通过PCR扩增出一个317 nt的产物。用该PCR产物筛选豌豆cDNA文库,获得了一个全长克隆。Northern分析显示存在一个1.1 kb的单一转录本,在幼叶和生殖组织中高表达。该克隆编码一个232个氨基酸(26 kDa)的前体蛋白,包括一个80个氨基酸(9 kDa)的N端延伸。对推导的氨基酸序列分析证实了它与从纯化的成熟豌豆线粒体NDPK获得的序列一致。在分离的豌豆线粒体中进行的体外导入实验表明,27 kDa的前体被靶向并加工成16.5 kDa的成熟形式。对一些脊椎动物和植物NDPK同工型的系统发育分析表明,豌豆线粒体NDPK与拟南芥的NDPK3同工型以及菠菜的叶绿体NDPK III归为一类。我们认为,有可能根据不同NDPK同工型的亚细胞定位和来源设计一种新的分类方法。

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