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蓖麻和烟草中质体丙酮酸激酶的分子特征

Molecular characterization of plastid pyruvate kinase from castor and tobacco.

作者信息

Blakeley S, Gottlob-McHugh S, Wan J, Crews L, Miki B, Ko K, Dennis D T

机构信息

Department of Biology, Queens University, Kingston, Ontario, Canada.

出版信息

Plant Mol Biol. 1995 Jan;27(1):79-89. doi: 10.1007/BF00019180.

Abstract

Clones encoding two different forms of plastid pyruvate kinase (PKp; EC 2.7.1.40) have been isolated from both castor and tobacco seed cDNA libraries. One form, designated PKpA, from castor was described in a previous report, and the tobacco homologue of PKpA has now been isolated. In addition, a second cDNA, designated PKpG, has been identified and sequenced in both species. Western blot analysis, using antibodies raised against protein overexpressed from these clones, indicates that they encode the two predominant polypeptides of plastid pyruvate kinase from developing castor endosperm. In castor, both PKpA and PKpG are encoded by single genes. In the allotetraploid Nicotiana tabacum, there are two copies of each, one derived from each of the progenitors of this species. The expression of the genes for PKpA and PKpG was examined in various tissues from both castor and tobacco. In castor, both forms are expressed in developing and germinating endosperm and in the root but neither is expressed in the leaf. In tobacco, both forms are expressed in developing seeds but in mature tissues, PKpA is most abundant in roots and PKpG in leaves.

摘要

已从蓖麻和烟草种子cDNA文库中分离出编码两种不同形式质体丙酮酸激酶(PKp;EC 2.7.1.40)的克隆。一种形式,来自蓖麻的命名为PKpA,已在先前的报告中描述,并且现已分离出PKpA的烟草同源物。此外,在这两个物种中均已鉴定并测序了第二个cDNA,命名为PKpG。使用针对这些克隆过表达的蛋白质产生的抗体进行的蛋白质印迹分析表明,它们编码发育中的蓖麻胚乳中质体丙酮酸激酶的两种主要多肽。在蓖麻中,PKpA和PKpG均由单个基因编码。在异源四倍体烟草中,每种都有两个拷贝,一个来自该物种的每个祖先。研究了蓖麻和烟草不同组织中PKpA和PKpG基因的表达。在蓖麻中,两种形式均在发育中和发芽的胚乳以及根中表达,但在叶中均不表达。在烟草中,两种形式均在发育中的种子中表达,但在成熟组织中,PKpA在根中最丰富,PKpG在叶中最丰富。

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