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Response of Pseudomonas putida KT2440 to Increased NADH and ATP Demand

机译:恶臭假单胞菌KT2440对NADH和ATP需求增加的响应

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Adenosine phosphate and NAD cofactors play a vital role in the operation of cell metabolism, and their levels and ratios are carefully regulated in tight ranges. Perturbations of the consumption of these metabolites might have a great impact on cell metabolism and physiology. Here, we investigated the impact of increased ATP hydrolysis and NADH oxidation rates on the metabolism of Pseudomonas putida KT2440 by titration of 2,4-dinitrophenol (DNP) and overproduction of a water-forming NADH oxidase, respectively. Both perturbations resulted in a reduction of the biomass yield and, as a consequence of the uncoupling of catabolic and anabolic activities, in an amplification of the net NADH regeneration rate. However, a stimulation of the specific carbon uptake rate was observed only when P. putida was challenged with very high 2,4-dinitrophenol concentrations and was comparatively unaffected by recombinant NADH oxidase activity. This behavior contrasts with the comparably sensitive performance described, for example, for Escherichia coli or Saccharomyces cerevisiae. The apparent robustness of P. putida metabolism indicates that it possesses a certain buffering capacity and a high flexibility to adapt to and counteract different stresses without showing a distinct phenotype. These findings are important, e.g., for the development of whole-cell redox biocatalytic processes that impose equivalent burdens on the cell metabolism: stoichiometric consumption of (reduced) redox cofactors and increased energy expenditures, due to the toxicity of the biocatalytic compounds.
机译:磷酸腺苷和NAD辅助因子在细胞代谢过程中起着至关重要的作用,并且它们的水平和比例在狭窄的范围内受到严格调节。这些代谢物消耗的扰动可能对细胞代谢和生理产生很大影响。在这里,我们分别通过滴定2,4-二硝基苯酚(DNP)和过量生成水的NADH氧化酶,研究了增加的ATP水解和NADH氧化速率对恶臭假单胞菌KT2440代谢的影响。两种干扰都导致生物量产量的降低,并且由于分解代谢和合成代谢活性的解偶联导致净NADH再生速率的增加。然而,仅当恶臭假单胞菌以非常高的2,4-二硝基苯酚浓度攻击并且相对不受重组NADH氧化酶活性影响时,才观察到比碳吸收率的刺激。该行为与例如针对大肠杆菌或啤酒酵母描述的相对敏感的性能形成对比。恶臭假单胞菌代谢的明显健壮性表明,它具有一定的缓冲能力和高度的适应性,可以在不显示明显表型的情况下适应和应对不同的压力。这些发现对于例如开发全细胞氧化还原生物催化过程非常重要,该过程会给细胞代谢带来同等的负担:由于生物催化化合物的毒性,化学计量消耗的(还原的)氧化还原辅因子和增加的能量消耗。

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