Bond D R, Russell J B
Section of Microbiology, Cornell University, Ithaca, New York 14853, USA.
Appl Environ Microbiol. 1998 Mar;64(3):976-81. doi: 10.1128/AEM.64.3.976-981.1998.
When the rate of glucose addition to nongrowing Streptococcus bovis cell suspensions was increased, the fermentation was homolactic, fructose-1,6-diphosphate (FDP) increased, intracellular inorganic phosphate (P(i)) declined, and the energy-spilling rate increased. ATP and ADP were not significantly affected by glucose consumption rate, but the decrease in P(i) was sufficient to cause an increase in the free energy of ATP hydrolysis (delta G'p). The increase in delta G'p was correlated with an increase in proton motive force (delta p). S. bovis continuous cultures (dilution rate of 0.65 h-1) that were provided with ammonia as the sole nitrogen source also had high rates of lactate production and energy spilling. When Trypticase was added as a source of amino acids, lactate production decreased; a greater fraction of the glucose was converted to acetate, formate, and ethanol; and the energy-spilling rate decreased. Trypticase also caused a decrease in FDP, an increase in P(i), and a decrease in delta p. The change in delta p could be explained by P(i)-dependent changes in the delta G'p. When P(i) declined, delta G'p and delta p increased. The ratio of delta G'p to delta p (millivolt per millivolt) was always high (> 4) at low rates of energy spilling but declined when the energy-spilling rate increased. Based on these results, it appears that delta p and the energy-spilling rate are responsive to fluctuations in the intracellular P(i) concentration.
当向非生长状态的牛链球菌细胞悬液中添加葡萄糖的速率增加时,发酵为同型乳酸发酵,果糖 - 1,6 - 二磷酸(FDP)增加,细胞内无机磷酸盐(P(i))下降,能量溢出率增加。ATP和ADP不受葡萄糖消耗速率的显著影响,但P(i)的下降足以导致ATP水解自由能(ΔG'p)增加。ΔG'p的增加与质子动力势(Δp)的增加相关。以氨作为唯一氮源的牛链球菌连续培养物(稀释率为0.65 h⁻¹)也具有较高的乳酸产生率和能量溢出率。当添加胰蛋白酶作为氨基酸来源时,乳酸产生减少;更大比例的葡萄糖转化为乙酸、甲酸和乙醇;并且能量溢出率降低。胰蛋白酶还导致FDP减少,P(i)增加,以及Δp降低。Δp的变化可以用P(i)依赖的ΔG'p变化来解释。当P(i)下降时,ΔG'p和Δp增加。在低能量溢出率下,ΔG'p与Δp的比值(毫伏每毫伏)始终很高(>4),但当能量溢出率增加时该比值下降。基于这些结果,似乎Δp和能量溢出率对细胞内P(i)浓度的波动有响应。