Bae W, Rittmann B E
National Institute of Environmental Research, Seoul 122-040, Republic of Korea.
Biotechnol Bioeng. 1996 Mar 20;49(6):690-9. doi: 10.1002/(SICI)1097-0290(19960320)49:6<690::AID-BIT11>3.0.CO;2-A.
The highly systematic responses of cellular cofactors to controlled substrate limitations of electron donor, electron acceptor, and both (dual limitation) were quantified using continuous-flow cultures of Pseudomonas putida. The results showed that the NADH concentration in the cells decreased gradually as the specific rate of electron-donor utilization (-q(d)) fell or increased systematically as oxygen limitation became more severe for fixed -q(d), while the NAD concentration was invariant. The NAD(H) responses demonstrated a common strategy; compensation for a low concentration of an externally supplied substrate by increasing (or decreasing) the concentration of its internal cosubstrate (or coproduct). The compensation was dramatic, as the NAD/NADH ratio showed a 24-fold modulation in response to depletion of dissolved oxygen (DO) or acetate. In the dual-limitation region, the compensating effects toward depletion of one substrate were damped, because the other substrate was simultaneously at low concentration. However, the NAD(H) responses minimized the adverse impact from substrate depletion on overall cell metabolism. Cellular contents of ATP, ADP, and P(i) were mostly affected by -q(d), such that the phosphorylation potential, ATP/ADP . P(i), increased as -q(d) fell due to depletion of acetate, DO, or both. Since the respiration rate should be slowed by high ATP/ADP . P(i), the cellular response seems to amplify an unfavorable environmental condition when oxygen is depleted. The likely reason for this apparent disadvantageous response is that the response of phosphorylation potential is more keenly associated with other aspects of metabolic control, such as for synthesis, which requires P(i) for production of phospholipids and nucleotides. (c) 1996 John Wiley & Sons, Inc.
利用恶臭假单胞菌的连续流培养对细胞辅因子针对电子供体、电子受体及二者(双重限制)的受控底物限制的高度系统性响应进行了量化。结果表明,随着电子供体利用比速率(-q(d))下降,细胞内的NADH浓度逐渐降低;而对于固定的-q(d),随着氧限制变得更加严重,NADH浓度则系统性升高,同时NAD浓度保持不变。NAD(H)响应展示了一种通用策略:通过增加(或减少)其内部共底物(或共产物)的浓度来补偿外部供应底物的低浓度。这种补偿作用显著,因为NAD/NADH比值在响应溶解氧(DO)或乙酸盐耗尽时呈现出24倍的调节。在双重限制区域,对一种底物耗尽的补偿作用受到抑制,因为另一种底物同时处于低浓度。然而,NAD(H)响应将底物耗尽对整体细胞代谢的不利影响降至最低。ATP、ADP和P(i)的细胞含量主要受-q(d)影响,使得磷酸化电位ATP/ADP·P(i)随着因乙酸盐、DO或二者耗尽导致的-q(d)下降而升高。由于高ATP/ADP·P(i)会使呼吸速率减慢,当氧耗尽时,细胞反应似乎会放大不利的环境条件。这种明显不利反应的可能原因是磷酸化电位的反应与代谢控制的其他方面,如合成,更密切相关,合成需要P(i)来生产磷脂和核苷酸。(c) 1996约翰威立国际出版公司