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豌豆叶绿体核苷二磷酸激酶:纯化、cDNA克隆及导入叶绿体

Nucleoside diphosphate kinase from pea chloroplasts: purification, cDNA cloning and import into chloroplasts.

作者信息

Lübeck J, Soll J

机构信息

Botanisches Institut, Christian-Albrechts-Universität, Kiel, Germany.

出版信息

Planta. 1995;196(4):668-73.

PMID:7580854
Abstract

Nucleoside diphosphate kinase (NDPK; EC 2.7.4.6) was enriched 1900-fold from purified pea (Pisum sativum L. cv. Golf.) chloroplasts. The active enzyme preparation contained two polypeptides of apparent molecular weight 18.5 kDa and 17.4 kDa. Both proteins were enzymatically active and were recognized by an antiserum raised against NDPK from spinach chloroplasts, suggesting the existence of two isoforms in pea chloroplasts. The N-terminal protein sequence data were obtained for both polypeptides and compared with the nucleotide sequence of a cDNA clone isolated from a pea cDNA library. The analysis revealed that the two NDPK forms are encoded for by one mRNA, indicating that the lower-molecular-weight form could represent a proteolytic breakdown product of the 18.5-kDa NDPK. The pea chloroplastic NDPK is made as a larger precursor protein which is imported into chloroplasts. The NDPK precursor is then processed by the stromal processing peptidase to yield the 18.5-kDa form.

摘要

核苷二磷酸激酶(NDPK;EC 2.7.4.6)从纯化的豌豆(Pisum sativum L. cv. Golf.)叶绿体中富集了1900倍。活性酶制剂包含两种表观分子量分别为18.5 kDa和17.4 kDa的多肽。这两种蛋白质都具有酶活性,并且能被针对菠菜叶绿体NDPK产生的抗血清识别,表明豌豆叶绿体中存在两种同工型。获得了这两种多肽的N端蛋白质序列数据,并与从豌豆cDNA文库中分离的一个cDNA克隆的核苷酸序列进行了比较。分析表明,两种NDPK形式由一个mRNA编码,这表明较低分子量的形式可能是18.5 kDa NDPK的蛋白水解产物。豌豆叶绿体NDPK最初作为一种较大的前体蛋白合成,该前体蛋白被导入叶绿体。然后,NDPK前体由基质加工肽酶加工,产生18.5 kDa的形式。

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