Havel C, Rector E R, Watson J A
J Biol Chem. 1986 Aug 5;261(22):10150-6.
Our previous studies (Watson, J. A., Havel, C. M., Lobos, D. V., Baker, F. C., and Morrow, C. J. (1985) J. Biol. Chem. 260, 14083-14091) suggested that a matabolite, distal to isopentenyl 1-pyrophospate (IPP), served as a regulatory signal for sterol-independent modulation of Kc cell 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase activity. This report summarizes efforts to localize the potential source of the post-IPP regulatory signal molecule. We found no direct correlation between mevalonate-mediated suppression of Kc cell HMG-CoA reductase activity and the rates of [1-14C]-, [3-14C]-, [5-14C]-, or [5-3H]mevalonate incorporation into either carbon dioxide, neutral lipids, water, or water-soluble isopentenoid pyrophosphate esters. [1-14C]Mevalonate's rate of conversion to 14CO2 (a measure of total isopentenyl 1-pyrophosphate synthesis) was minimally 5-fold greater than that for neutral isopentenoid lipid synthesis (measured with either [5-3H]-, [3-14C]-, or [5-14C]mevalonate). However, [5-3H]mevalonate's rate of conversion into [3H]H2O (measure of shunted mevalonate carbon) was equivalent or greater than that measured for neutral isopentenoid lipid synthesis. [5-14C]Mevalonate radioactivity was incorporated into macromolecules and n-fatty acids. Kc cell extracts (100,000 X g supernatant fluid) readily oxidized alcohols with the following activity sequence: geraniol = nerol greater than farnesol = dimethylallyl alcohol greater than geranylgeraniol, isopentenyl alcohol, and allyl alcohol. Oxidation required NAD, and ethanol was not a substrate. We conclude that (a) Kc cells shunted a significant fraction (greater than or equal to 40%) of their post-IPP carbon to prenols for oxidative catabolism and (b) that shunted mevalonate carbon may play a significant role in the mevalonate-mediated regulation of Kc cell HMG-CoA reductase activity.
我们之前的研究(沃森,J.A.,哈维尔,C.M.,洛博斯,D.V.,贝克,F.C.,以及莫罗,C.J.(1985年)《生物化学杂志》260卷,14083 - 14091页)表明,异戊烯基焦磷酸(IPP)下游的一种代谢物作为一种调节信号,用于对Kc细胞3 - 羟基 - 3 - 甲基戊二酰辅酶A(HMG - CoA)还原酶活性进行不依赖于固醇的调节。本报告总结了确定IPP后调节信号分子潜在来源的研究工作。我们发现,甲羟戊酸介导的对Kc细胞HMG - CoA还原酶活性的抑制作用,与[1 - 14C] -、[3 - 14C] -、[5 - 14C] - 或[5 - 3H]甲羟戊酸掺入二氧化碳、中性脂质、水或水溶性异戊烯类焦磷酸酯的速率之间没有直接关联。[1 - 14C]甲羟戊酸转化为14CO2的速率(衡量异戊烯基焦磷酸总合成量的指标)至少比中性异戊烯类脂质合成速率(用[5 - 3H] -、[3 - 14C] - 或[5 - 14C]甲羟戊酸测量)高5倍。然而,[5 - 3H]甲羟戊酸转化为[3H]H2O的速率(衡量分流的甲羟戊酸碳量的指标)与中性异戊烯类脂质合成速率相当或更高。[5 - 14C]甲羟戊酸的放射性被掺入大分子和n - 脂肪酸中。Kc细胞提取物(100,000×g上清液)能轻易氧化醇类,其活性顺序如下:香叶醇 = 橙花醇>法呢醇 = 二甲基烯丙醇>香叶基香叶醇、异戊烯醇和烯丙醇。氧化反应需要NAD,乙醇不是底物。我们得出结论:(a)Kc细胞将其IPP后碳的很大一部分(≥40%)分流至异戊烯醇用于氧化分解代谢;(b)分流的甲羟戊酸碳可能在甲羟戊酸介导的Kc细胞HMG - CoA还原酶活性调节中起重要作用。