Thompson S N, Lee R W
Analytical Chemistry Instrumentation Facility, University of California, Riverside 92521.
Biochim Biophys Acta. 1993 Jul 11;1157(3):259-69. doi: 10.1016/0304-4165(93)90108-k.
The fate of [3-13C]alanine administered to last instar larvae of an insect Manduca sexta was investigated in vivo by 13C-NMR spectroscopy. Following injection of the isotopically substituted substrate and conversion to [3-13C]pyruvate 13C was principally incorporated into C2, C3 and C4 of glutamate and glutamine in unparasitized ad libitum-fed larvae, insects starved 48 hr prior to injection and larvae parasitized by the insect parasite Cotesia congregata. Selective labeling at C2 and C3 of glutamate/glutamine resulted from carboxylation of [3-13C]pyruvate to [2,3-13C]oxaloacetate catalyzed by pyruvate carboxylase, randomization of the label in fumarate, and synthesis of glutamate and glutamine after condensation with acetyl CoA to [2 proR,3-13C]citrate. In contrast, enrichment at C4 of glutamate and glutamine resulted from oxidation [3-13C]pyruvate to [2-13C]acetyl CoA catalyzed by pyruvate dehydrogenase followed by condensation with oxaloacetate. The ratio of enrichment (C2 + C3): C4 provided a measure of the relative contributions of the pyruvate dehydrogenase and pyruvate carboxylase catalyzed pathways of substrate utilization by the tricarboxylic acid cycle. The mean ratio was 0.6 and 0.7 in control and parasitized larvae, respectively, and 2.4 in starved insects. The latter result demonstrated that substrate utilization by the TCA cycle was markedly altered by starvation. In addition, the rate of labeled alanine metabolism was significantly reduced by starvation. The concentrations of glutamate and glutamine in the blood (hemolymph) were similar in all three groups of insects. No evidence for gluconeogenesis was observed in any group. Starved larvae incorporated label into C6 of glucose and trehalose but no complementary enrichment at C1 was observed. This result was consistent with the activity of the non-oxidative phase of the pentose phosphate pathway during which labeled glyceraldehyde-3-phosphate arising from [3-13C]alanine reacts with sedoheptulose-7-phosphate yielding erythrose-4-phosphate and [6-13C]fructose-6-phosphate catalyzed by transaldolase. Specifically labeled fructose-6-phosphate then gives rise to glucose and trehalose labeled at C6. Preliminary analysis of the hemolymph of starved insects indicated the presence of several hexose phosphates labeled at C6. The hemolymph level of trehalose was significantly reduced in both starved and parasitized insects. Lipogenesis from [3-13C]alanine was evident in unparasitized control larvae but was absent in parasitized and starved insects. The pattern of labeling in fatty acid was consistent with de novo pathway utilizing [2-13C]acetyl CoA derived by oxidation of [3-13C]alanine.
通过¹³C - NMR光谱法在体内研究了给烟草天蛾末龄幼虫注射[3 - ¹³C]丙氨酸后的命运。在未寄生的自由取食幼虫、注射前饥饿48小时的昆虫以及被昆虫寄生虫聚瘤姬蜂寄生的幼虫中,注射同位素取代的底物并转化为[3 - ¹³C]丙酮酸后,¹³C主要掺入谷氨酸和谷氨酰胺的C2、C3和C4位。谷氨酸/谷氨酰胺C2和C3位的选择性标记源于丙酮酸羧化酶催化[3 - ¹³C]丙酮酸羧化为[2,3 - ¹³C]草酰乙酸,富马酸中标记的随机化,以及与乙酰辅酶A缩合为[2 proR,3 - ¹³C]柠檬酸后谷氨酸和谷氨酰胺的合成。相反,谷氨酸和谷氨酰胺C4位的富集源于丙酮酸脱氢酶催化[3 - ¹³C]丙酮酸氧化为[2 - ¹³C]乙酰辅酶A,随后与草酰乙酸缩合。富集比(C2 + C3): C4提供了三羧酸循环中丙酮酸脱氢酶和丙酮酸羧化酶催化的底物利用途径相对贡献的一种度量。对照组和寄生幼虫中的平均比值分别为0.6和0.7,饥饿昆虫中的平均比值为2.4。后一结果表明饥饿显著改变了三羧酸循环的底物利用。此外,饥饿显著降低了标记丙氨酸的代谢速率。三组昆虫血淋巴中谷氨酸和谷氨酰胺的浓度相似。在任何一组中均未观察到糖异生的证据。饥饿幼虫将标记掺入葡萄糖和海藻糖的C6位,但未观察到C1位的互补富集。该结果与磷酸戊糖途径非氧化阶段的活性一致,在此期间,由[3 - ¹³C]丙氨酸产生的标记3 - 磷酸甘油醛与景天庚酮糖 - 7 - 磷酸反应,在转醛醇酶催化下生成赤藓糖 - 4 - 磷酸和[6 - ¹³C]果糖 - 6 - 磷酸。具体标记的果糖 - 6 - 磷酸随后产生在C6位标记的葡萄糖和海藻糖。对饥饿昆虫血淋巴的初步分析表明存在几种在C6位标记的己糖磷酸。饥饿和寄生昆虫中海藻糖的血淋巴水平均显著降低。在未寄生的对照幼虫中,[3 - ¹³C]丙氨酸的脂肪生成明显,但在寄生和饥饿昆虫中不存在。脂肪酸中的标记模式与利用[3 - ¹³C]丙氨酸氧化衍生的[2 - ¹³C]乙酰辅酶A的从头合成途径一致。