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卤虫休眠胚胎中二(5'-核苷基)四磷酸焦磷酸水解酶的特性研究

Characterization of the bis(5'-nucleosidyl) tetraphosphate pyrophosphohydrolase from encysted embryos of the brine shrimp Artemia.

作者信息

Prescott M, Milne A D, McLennan A G

机构信息

Department of Biochemistry, University of Liverpool, U.K.

出版信息

Biochem J. 1989 May 1;259(3):831-8. doi: 10.1042/bj2590831.

Abstract

The P1P4-bis(5'-nucleosidyl) tetraphosphate asymmetrical-pyrophosphohydrolase from encysted embryos of the brine shrimp Artemia has been purified over 11,000-fold to homogeneity. Anion-exchange chromatography resolves two major species with very similar properties. The enzyme is a single polypeptide of Mr 17,600 and is maximally active at pH 8.4 and 2 mM-Mg2+. It is inhibited by Ca2+ (IC50 = 0.9 mM with 2 mM-Mg2+) but not by Zn2+ ions. It preferentially hydrolyses P1P4-bis(5'-nucleosidyl) tetraphosphates, e.g. P1P4-bis(5'-adenosyl) tetraphosphate (Ap4A) (kcat. = 12.7 s-1; Km = 33 microM) and P1P4-bis(5'-guanosyl) tetraphosphate (Gp4G) (kcat. = 6.2 s-1; Km = 5 microM). With adenosine 5'-P1-tetraphospho-P4-5"'-guanosine (Ap4G) as substrate, there is a 4.5-fold preference for AMP and GTP as products and biphasic reaction kinetics are observed giving Km values of 4.7 microM and 34 microM, and corresponding rate constants of 6.5 s-1 and 11.9 s-1. The net rate constant for Ap4G hydrolysis is 7.6 s-1. The enzyme will also hydrolyse nucleotides with more than four phosphate groups, e.g. Ap5G, Ap6A and Gp5G are hydrolysed at 25%, 18% and 10% of the rate of Ap4A respectively. An NTP is always one of the products. Ap2A and Gp2G are not hydrolysed, while Ap3A and Gp3G are very poor substrates. When the enzyme is partially purified from embryos and larvae at different stages of development by sedimentation through a sucrose density gradient, its activity increases 3-fold during the first 12 h of pre-emergence development. This is followed by a slow decline during subsequent larval development. The similarity of this enzyme to other asymmetrical-pyrophosphohydrolases suggests that it did not evolve specifically to degrade the large yolk platelet store of Gp4G which is found in Artemia embryos, but that it probably serves the same general function in bis(5'-nucleosidyl) oligophosphate metabolism as in other cells.

摘要

从卤虫(Artemia)包囊胚胎中提取的P1P4 - 双(5'-核苷基)四磷酸不对称焦磷酸水解酶已被纯化至超过11000倍的纯度,达到同质状态。阴离子交换色谱法分离出两种性质非常相似的主要成分。该酶是一种分子量为17600的单条多肽链,在pH 8.4和2 mM - Mg2+条件下活性最高。它受到Ca2+的抑制(在2 mM - Mg2+存在时IC50 = 0.9 mM),但不受Zn2+离子的抑制。它优先水解P1P4 - 双(5'-核苷基)四磷酸,例如P1P4 - 双(5'-腺苷基)四磷酸(Ap4A)(kcat. = 12.7 s-1;Km = 33 microM)和P1P4 - 双(5'-鸟苷基)四磷酸(Gp4G)(kcat. = 6.2 s-1;Km = 5 microM)。以腺苷5'-P1 - 四磷酸 - P4 - 5'''-鸟苷(Ap4G)作为底物时,产物中AMP和GTP的生成偏好性为4.5倍,并且观察到双相反应动力学,Km值分别为4.7 microM和34 microM,相应的速率常数分别为6.5 s-1和11.9 s-1。Ap4G水解的净速率常数为7.6 s-1。该酶还能水解具有四个以上磷酸基团的核苷酸,例如Ap5G、Ap6A和Gp5G的水解速率分别为Ap4A的25%、18%和10%。NTP始终是产物之一。Ap2A和Gp2G不被水解,而Ap3A和Gp3G是非常差的底物。当通过蔗糖密度梯度沉降从不同发育阶段的胚胎和幼虫中对该酶进行部分纯化时,其活性在孵化前发育的最初12小时内增加3倍。随后在幼虫发育过程中缓慢下降。这种酶与其他不对称焦磷酸水解酶的相似性表明,它并非专门为降解卤虫胚胎中发现的大量卵黄血小板储存的Gp4G而进化,而是可能在双(5'-核苷基)寡磷酸代谢中发挥与其他细胞相同的一般功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9f5/1138592/6d65e666fd67/biochemj00208-0199-a.jpg

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