HAROLD F M
J Bacteriol. 1962 May;83(5):1047-57. doi: 10.1128/jb.83.5.1047-1057.1962.
Harold, F. M. (National Jewish Hospital, Denver, Colo.). Depletion and replenishment of the inorganic polyphosphate pool in Neurospora crassa. J. Bacteriol. 83:1047-1057. 1962.-Turnover of the inorganic polyphosphate pool of Neurospora crassa was demonstrated in both growing and nongrowing mycelium. In nitrogen-deficient cultures, polyphosphate synthesis and degradation were in balance and no net changes occurred. When mycelium was suspended in a growth medium deficient in phosphate, polyphosphate was degraded to acid-soluble compounds, including adenosine triphosphate (ATP) and orthophosphate; net synthesis of nucleic acids and phospholipids occurred at the expense of polyphosphate. Various attempts were made to demonstrate direct formation of ATP from polyphosphate when oxidative and fermentative ATP generation were blocked. No evidence for this reaction could be obtained, suggesting that the primary product of polyphosphate degradation is not ATP but probably orthophosphate. Addition of phosphate to phosphate-starved mycelium induced rapid replenishment of the polyphosphate pool; polyphosphate accumulation ceased abruptly when the original level had been restored. The finding that ATP accumulation within the mycelium preceded polyphosphate synthesis, together with the rapid turnover of this compound, supports the view that ATP is the metabolic precursor of polyphosphate. The results suggest a cyclic pattern of polyphosphate metabolism. In N. crassa at least, polyphosphate does not appear to function as a reservoir of "high-energy" phosphate, but the polyphosphate cycle may be involved in the dissipation of excess ATP.
哈罗德,F.M.(科罗拉多州丹佛市国家犹太医院)。粗糙脉孢菌中无机多聚磷酸盐库的消耗与补充。《细菌学杂志》83:1047 - 1057。1962年。——在生长和不生长的菌丝体中均证明了粗糙脉孢菌无机多聚磷酸盐库的周转。在缺氮培养物中,多聚磷酸盐的合成与降解处于平衡状态,没有净变化发生。当菌丝体悬浮于缺磷的生长培养基中时,多聚磷酸盐被降解为酸溶性化合物,包括三磷酸腺苷(ATP)和正磷酸盐;核酸和磷脂的净合成以多聚磷酸盐为代价发生。当氧化和发酵产生ATP被阻断时,进行了各种尝试以证明由多聚磷酸盐直接形成ATP。未获得该反应的证据,这表明多聚磷酸盐降解的主要产物不是ATP,而可能是正磷酸盐。向缺磷的菌丝体中添加磷酸盐会诱导多聚磷酸盐库的快速补充;当恢复到原始水平时,多聚磷酸盐的积累会突然停止。菌丝体内ATP积累先于多聚磷酸盐合成这一发现,以及该化合物的快速周转,支持了ATP是多聚磷酸盐代谢前体的观点。结果表明了多聚磷酸盐代谢的循环模式。至少在粗糙脉孢菌中,多聚磷酸盐似乎并不作为“高能”磷酸盐的储存库起作用,但多聚磷酸盐循环可能参与了过量ATP的消耗。