Kodaki T, Murakami H, Taguchi M, Izui K, Katsuki H
J Biochem. 1981 Nov;90(5):1437-44. doi: 10.1093/oxfordjournals.jbchem.a133610.
A large amount of pyruvate was excreted into the medium by CP78 (rel+) cells grown on succinate when they were starved for amino acids. In contrast, no such excretion was observed with CP79 (rel-) cells. This phenomenon was also seen with two other isogenic pairs of strains: NF161 (rel+) and NF162 (rel-), and 10B601 (rel+) and 10B602 (rel-). Besides succinate, L-malate, and fumarate were effective carbon sources for the excretion, but glucose, glycerol, and acetate were not. When DL-lactate was used, not only CP78 but also CP79 cells excreted pyruvate. Experiments using [1,4-14C]succinate as a carbon source revealed that pyruvate was formed by decarboxylation of one carboxyl group of succinate and that the pyruvate excretion amounted to about 40% of the total succinate degraded. Experiments designed to elucidate the mechanism of the excretion yielded the following observations. (i) The concentration of pyruvate in CP78 cells grown on the C4-dicarboxylic acids mentioned above was not significantly changed upon amino acid starvation. (ii) Guanosine 5'-diphosphate-3'-diphosphate exerted no effect on the activities of several enzymes thought to be involved in pyruvate-related metabolism. It is suggested firstly that the excretion was not due to some impairment in the biosynthetic pathway of a particular amino acid, but was due to the stringent control of central amphibolic metabolism, and secondly that no de novo protein synthesis was involved in the excretion.
当在琥珀酸上生长的CP78(rel +)细胞缺乏氨基酸时,大量丙酮酸被排泄到培养基中。相比之下,CP79(rel -)细胞未观察到这种排泄现象。在另外两对同基因菌株中也观察到了这种现象:NF161(rel +)和NF162(rel -),以及10B601(rel +)和10B602(rel -)。除琥珀酸外,L-苹果酸和富马酸是促进排泄的有效碳源,但葡萄糖、甘油和乙酸不是。当使用DL-乳酸时,不仅CP78细胞,CP79细胞也排泄丙酮酸。以[1,4 - 14C]琥珀酸作为碳源的实验表明,丙酮酸是由琥珀酸的一个羧基脱羧形成的,丙酮酸排泄量约占降解的琥珀酸总量的40%。旨在阐明排泄机制的实验得出了以下观察结果。(i)在上述C4 - 二羧酸上生长的CP78细胞中,丙酮酸浓度在氨基酸饥饿时没有显著变化。(ii)鸟苷5'-二磷酸-3'-二磷酸对几种被认为参与丙酮酸相关代谢的酶的活性没有影响。首先表明,排泄不是由于特定氨基酸生物合成途径的某些损伤,而是由于中心两用代谢的严格控制,其次表明排泄过程中不涉及从头蛋白质合成。