Davis R H, Ristow J L
J Biol Chem. 1987 May 25;262(15):7109-17.
Citrulline is synthesized in mitochondria of Neurospora crassa from ornithine and carbamoyl phosphate. In mycelia grown in minimal medium, carbamoyl phosphate limits citrulline (and arginine) synthesis. Addition of arginine to such cultures reduces the availability of intramitochondrial ornithine, and ornithine then limits citrulline synthesis. We have found that for some time after addition of excess arginine, carbamoyl phosphate synthesis continued. Very little of this carbamoyl phosphate escaped the mitochondrion to be used in the pyrimidine pathway in the nucleus. Instead, mitochondrial carbamoyl phosphate accumulated over 40-fold and turned over rapidly. This was true in ornithine- or ornithine carbamoyltransferase-deficient mutants and in normal mycelia during feedback inhibition of ornithine synthesis. The data suggest that the rate of carbamoyl phosphate synthesis is dependent to a large extent upon the specific activity of the slowly and incompletely repressible synthetic enzyme, carbamoyl-phosphate synthetase A. In keeping with this conclusion, we found that when carbamoyl-phosphate synthetase A was repressed 2-10-fold by growth of mycelia in arginine, carbamoyl phosphate was still synthesized in excess of that used for residual citrulline synthesis. Again, only a small fraction of the excess carbamoyl phosphate could be accounted for by diversion to the pyrimidine pathway. The continued synthesis and turnover of carbamoyl phosphate in mitochondria of arginine-grown cells may allow rapid resumption of citrulline formation after external arginine disappears and no longer exerts negative control on ornithine biosynthesis.
瓜氨酸在粗糙脉孢菌的线粒体中由鸟氨酸和氨甲酰磷酸合成。在基本培养基中生长的菌丝体中,氨甲酰磷酸限制瓜氨酸(和精氨酸)的合成。向此类培养物中添加精氨酸会降低线粒体内鸟氨酸的可用性,然后鸟氨酸会限制瓜氨酸的合成。我们发现,在添加过量精氨酸后的一段时间内,氨甲酰磷酸的合成仍在继续。这种氨甲酰磷酸很少逸出线粒体而用于细胞核中的嘧啶途径。相反,线粒体氨甲酰磷酸积累了40多倍并迅速周转。在鸟氨酸或鸟氨酸氨甲酰转移酶缺陷型突变体以及正常菌丝体在鸟氨酸合成的反馈抑制过程中都是如此。数据表明,氨甲酰磷酸的合成速率在很大程度上取决于缓慢且不完全可抑制的合成酶氨甲酰磷酸合成酶A的比活性。与此结论一致,我们发现,当菌丝体在精氨酸中生长使氨甲酰磷酸合成酶A被抑制2至10倍时,氨甲酰磷酸的合成量仍超过用于残余瓜氨酸合成的量。同样,过量氨甲酰磷酸中只有一小部分可通过转向嘧啶途径来解释。在精氨酸生长的细胞的线粒体中氨甲酰磷酸的持续合成和周转可能使外部精氨酸消失且不再对鸟氨酸生物合成施加负调控后,瓜氨酸的形成能够迅速恢复。