Moody A J, West I C, Mitchell R, Mitchell P
Eur J Biochem. 1986 Jun 2;157(2):243-9. doi: 10.1111/j.1432-1033.1986.tb09662.x.
The observation in this laboratory that respiration and Sr2+ import were stimulated by the addition of 3-hydroxybutyrate to suspensions of N-ethylmaleimide-treated mitochondria respiring in state 6, after the addition of Sr2+, in a sucrose medium containing choline as substrate, led to the proposal by Moyle and Mitchell [(1977) FEBS Lett. 84, 135-140] that there is a Ca2+(Sr2+)-3-hydroxybutyrate symporter in rat liver mitochondria. However, experiments described in the present paper support a different interpretation. Under the conditions of the experiments by Moyle and Mitchell, the rate of respiration and the poise of Sr2+ accumulation are mainly limited, not by delta mu H+, but by lack of respiratory substrate. Even though N-ethylmaleimide is a potent inhibitor of 3-hydroxybutyrate dehydrogenase, we have found that, somewhat surprisingly, under the special conditions of these experiments, sufficient 3-hydroxybutyrate dehydrogenase activity remains available to account for the 3-hydroxybutyrate-dependent respiratory stimulation and Sr2+ import.
本实验室观察到,在以胆碱为底物的蔗糖培养基中,于状态6呼吸的经N - 乙基马来酰亚胺处理的线粒体悬液中加入Sr²⁺后,再添加3 - 羟基丁酸可刺激呼吸和Sr²⁺的摄取,由此莫伊尔和米切尔[(1977年)《欧洲生物化学学会联合会快报》84卷,第135 - 140页]提出大鼠肝线粒体中存在Ca²⁺(Sr²⁺)- 3 - 羟基丁酸同向转运体。然而,本文所述实验支持另一种解释。在莫伊尔和米切尔的实验条件下,呼吸速率和Sr²⁺积累的平衡主要受限于缺乏呼吸底物,而非质子动力势。尽管N - 乙基马来酰亚胺是3 - 羟基丁酸脱氢酶的有效抑制剂,但我们发现,有些出人意料的是,在这些实验的特殊条件下,仍有足够的3 - 羟基丁酸脱氢酶活性可解释3 - 羟基丁酸依赖的呼吸刺激和Sr²⁺摄取。