Grammel Hartmut, Gilles Ernst-Dieter, Ghosh Robin
Max Planck Institute for Dynamics of Complex Technical Systems, D-39106 Magdeburg, Germany. grammel@,pi-magdeburg.mpg.de
Appl Environ Microbiol. 2003 Nov;69(11):6577-86. doi: 10.1128/AEM.69.11.6577-6586.2003.
The purple nonsulfur bacterium Rhodospirillum rubrum has been employed to study physiological adaptation to limiting oxygen tensions (microaerophilic conditions). R. rubrum produces maximal levels of photosynthetic membranes when grown with both succinate and fructose as carbon sources under microaerophilic conditions in comparison to the level (only about 20% of the maximum) seen in the absence of fructose. Employing a unique partial O(2) pressure (pO(2)) control strategy to reliably adjust the oxygen tension to values below 0.5%, we have used bioreactor cultures to investigate the metabolic rationale for this effect. A metabolic profile of the central carbon metabolism of these cultures was obtained by determination of key enzyme activities under microaerophilic as well as aerobic and anaerobic phototrophic conditions. Under aerobic conditions succinate and fructose were consumed simultaneously, whereas oxygen-limiting conditions provoked the preferential breakdown of fructose. Fructose was utilized via the Embden-Meyerhof-Parnas pathway. High levels of pyrophosphate-dependent phosphofructokinase activity were found to be specific for oxygen-limited cultures. No glucose-6-phosphate dehydrogenase activity was detected under any conditions. We demonstrate that NADPH is supplied mainly by the pyridine-nucleotide transhydrogenase under oxygen-limiting conditions. The tricarboxylic acid cycle enzymes are present at significant levels during microaerophilic growth, albeit at lower levels than those seen under fully aerobic growth conditions. Levels of the reductive tricarboxylic acid cycle marker enzyme fumarate reductase were also high under microaerophilic conditions. We propose a model by which the primary "switching" of oxidative and reductive metabolism is performed at the level of the tricarboxylic acid cycle and suggest how this might affect redox signaling and gene expression in R. rubrum.
紫色非硫细菌深红红螺菌已被用于研究对有限氧张力(微需氧条件)的生理适应性。与在没有果糖的情况下所观察到的水平(仅为最大值的约20%)相比,深红红螺菌在微需氧条件下以琥珀酸和果糖作为碳源生长时,会产生最大水平的光合膜。通过采用独特的部分氧分压(pO₂)控制策略,将氧张力可靠地调节至低于0.5%的值,我们利用生物反应器培养来研究这种效应的代谢原理。通过测定微需氧以及有氧和厌氧光养条件下的关键酶活性,获得了这些培养物中心碳代谢的代谢谱。在有氧条件下,琥珀酸和果糖同时被消耗,而氧限制条件则引发果糖的优先分解。果糖通过糖酵解途径被利用。发现高水平的焦磷酸依赖性磷酸果糖激酶活性是氧限制培养物所特有的。在任何条件下均未检测到葡萄糖-6-磷酸脱氢酶活性。我们证明,在氧限制条件下,NADPH主要由吡啶核苷酸转氢酶提供。三羧酸循环酶在微需氧生长期间以显著水平存在,尽管其水平低于完全有氧生长条件下所见的水平。在微需氧条件下,还原性三羧酸循环标记酶延胡索酸还原酶的水平也很高。我们提出了一个模型,通过该模型,氧化代谢和还原代谢的主要“切换”在三羧酸循环水平上进行,并提出了这可能如何影响深红红螺菌中的氧化还原信号传导和基因表达。