Suppr超能文献

乌头酸酶:其催化质子的来源。

Aconitase: its source of catalytic protons.

作者信息

Kuo D J, Rose I A

机构信息

Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111.

出版信息

Biochemistry. 1987 Dec 1;26(24):7589-96. doi: 10.1021/bi00398a009.

Abstract

An ordinary isotope partition experiment was performed to determine the rate of dissociation of the proton from the donor site for the hydration of cis-aconitate. Aconitase in [3H]water was efficiently diluted into well-mixed solutions of cis-aconitate. Citrate and isocitrate that were formed within 2 s were more heavily labeled than could be explained by consideration of an isotope effect in the processing of one proton per enzyme equivalent. Control experiments indicate that mixing was much more rapid than catalytic turnover, ruling out incompletely diluted [3H]water as a significant isotope source. Therefore, it appears that significantly more than one enzyme-bound tritium atom (protons) must have been used in the course of the multiple turnover of the enzyme after the dilution was complete. Isotope incorporation reached values in excess of four proton equivalents as a limit with simple Michaelis dependence on cis-aconitate. From the half-saturation concentration value for trapping, 0.15 mM, the t 1/2 for exchange of each of these protons with solvent appears to be approximately 0.1 s at 0 degrees C. The large number of protons trapped seems to suggest the existence of a structurally stabilized pool of protons, or water, that communicates between the active site base and the medium in the hydration of cis-aconitate. The proton abstracted in the dehydration of [3H]citrate is transferred directly to undissociated cis-aconitate to form isocitrate without dilution, or cis-aconitate having dissociated, the tritium passes to the medium, presumably through the pool of bound protons indicated above. All of the citrate-derived protons can be found in isocitrate if cis-aconitate is added in sufficient concentration.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

进行了一项普通的同位素分配实验,以确定顺乌头酸水合过程中质子从供体部位解离的速率。将[³H]水中的乌头酸酶有效稀释到充分混合的顺乌头酸溶液中。在2秒内形成的柠檬酸和异柠檬酸的标记程度比考虑每酶当量处理一个质子时的同位素效应所能解释的要高得多。对照实验表明,混合比催化周转快得多,排除了未完全稀释的[³H]水作为重要同位素来源的可能性。因此,似乎在稀释完成后酶的多次周转过程中,使用的酶结合氚原子(质子)明显多于一个。随着对顺乌头酸的简单米氏依赖性,同位素掺入量达到超过四个质子当量的极限值。从捕获的半饱和浓度值0.15 mM来看,在0℃时,这些质子中每一个与溶剂交换的t1/2似乎约为0.1秒。捕获的大量质子似乎表明存在一个结构稳定的质子或水池,它在顺乌头酸水合过程中在活性部位碱基和介质之间进行沟通。[³H]柠檬酸脱水过程中提取的质子直接转移到未解离的顺乌头酸上形成异柠檬酸而不被稀释,或者如果顺乌头酸已经解离,氚则传递到介质中,大概是通过上述结合质子池。如果加入足够浓度的顺乌头酸,所有柠檬酸衍生的质子都可以在异柠檬酸中找到。(摘要截短于250字)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验