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来自秀丽白虾的一种新型精氨酸激酶:第四个精氨酸激酶基因谱系。

A novel arginine kinase from the shrimp Neocaridina denticulata: the fourth arginine kinase gene lineage.

作者信息

Iwanami Kentaro, Iseno Shin-ichi, Uda Kouji, Suzuki Tomohiko

机构信息

Laboratory of Biochemistry, Faculty of Science, Kochi University, Kochi 780-8520, Japan.

出版信息

Gene. 2009 May 15;437(1-2):80-7. doi: 10.1016/j.gene.2009.02.018. Epub 2009 Mar 5.

Abstract

Arginine kinases (AK) evolved independently at least three times: first at an early stage of phosphagen kinase evolution (typical AK), second from the cytoplasmic creatine kinase (CK) gene later in metazoan evolution (Stichopus AK) and third from the mitochondrial CK gene in the course of annelid radiation (Sabellastarte AK). Here, we present a possible fourth AK lineage. We amplified cDNA encoding three AKs (AK1, AK2 and AK3) from the shrimp Neocaridina denticulata, and determined their amino acid sequences (355-356 residues). Each cDNA sequence was cloned in a pET plasmid and the corresponding recombinant kinase was expressed in E. coli. The AKs showed monomeric nature similar to typical AKs on an analytical gel filtration column. While the amino acid sequence of AK2 corresponded to that of typical AK, containing the conserved key residues established in Limulus AK for the substrate binding site, those of AK1 and AK3 lacked some of these key residues, indicating a similar evolution to Stichopus and Sabellastarte AKs. Moreover, phylogenetic analysis of phosphagen kinases indicated that Neocaridina AK1 and AK3 diverged at the deepest branching point close to the root of the tree and formed a distinct cluster outside the typical AK cluster, which included Neocaridina AK2. Kinetic constants of Neocaridina AKs were similar to those of other AKs. However, activation energy (E(a)) for the transition state of AK1 and AK3 was about 1.5-fold larger than that of AK2. The DeltaH(o++) values for AK1 and AK3 were also about 1.5-fold larger than that for AK2, but all three DeltaG(o++) values were very similar (71-72 kJ/mol); this results in similar reaction velocities for the three AK reactions due to a lower decrease in entropy in the activated complexes of AK1 and AK3 reactions compared to that of AK2. These findings suggest that Neocaridina AK1 and AK3 are unique from the known three AK gene lineages and therefore comprises a fourth AK lineage.

摘要

精氨酸激酶(AK)至少独立进化了三次:第一次是在磷酸原激酶进化的早期阶段(典型的AK),第二次是在后生动物进化后期从细胞质肌酸激酶(CK)基因进化而来(刺参AK),第三次是在环节动物辐射过程中从线粒体CK基因进化而来(星虫AK)。在此,我们提出了一种可能的第四个AK谱系。我们从秀丽白虾中扩增出编码三种AK(AK1、AK2和AK3)的cDNA,并确定了它们的氨基酸序列(355 - 356个残基)。每个cDNA序列都克隆到一个pET质粒中,并在大肠杆菌中表达相应的重组激酶。在分析性凝胶过滤柱上,这些AK表现出与典型AK相似的单体性质。虽然AK2的氨基酸序列与典型AK的序列相对应,包含在鲎AK中确定的用于底物结合位点的保守关键残基,但AK1和AK3的氨基酸序列缺少其中一些关键残基,这表明它们与刺参和星虫AK有相似的进化过程。此外,磷酸原激酶的系统发育分析表明,秀丽白虾AK1和AK3在靠近树根部的最深分支点处分化,并在典型AK簇之外形成一个独特的簇,该簇包括秀丽白虾AK2。秀丽白虾AK的动力学常数与其他AK相似。然而,AK1和AK3过渡态的活化能(E(a))比AK2大约1.5倍。AK1和AK3的ΔH(o++)值也比AK2大约1.5倍,但所有三个ΔG(o++)值非常相似(71 - 72 kJ/mol);这导致三个AK反应的反应速度相似,因为与AK2相比,AK1和AK3反应的活化复合物中的熵降低较少。这些发现表明,秀丽白虾AK1和AK3不同于已知的三个AK基因谱系,因此构成了第四个AK谱系。

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