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Kinetics of High Concentrated Phenol Biodégradation by Acinetobacter Baumannii

机译:八甘笼杆菌高浓度酚生物学的动力学

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Acinetobacter baumannii was isolated and tested for phenol degradation.This bacterium has high phenol degradation activity and high tolerance to phenol. The biodégradation assays were performed in liquid medium with the phenol as single substrate. Different concentrations of phenol samples ranging from 125 mg/lit to 1000 mg/lit were taken for observations. The bioremediation potential of an indigenous Acinetobacter baumanniiwas studied in batch culture using synthetic phbnol in water in the concentration range of (125 -1000) mg/L as a limiting substrate. The effect of initial phenol concentration on the degradation process was investigated.Phenol was completely degraded at different cultivation times with different initial phenol concentrations. Increasing the initial phenol concentration from 125 mg/L to 1000 mg/L increased the lag phase from 0 to 48 h and correspondingly prolonged the degradation process from 84 h to 354 h. There was decrease in biodégradation rate as initial phenol concentration increased. Fitting data into Monod kinetic model showed the inhibition effect of phenol. The kinetic parameters have been estimated.The rsmax decreased and Ks increased with higher concentration of phenol. The rsmax has been found to be a strong function of initial phenol concentration. The culture followed substrate inhibition kinetics and the specific phenol consumption rates were fitted to Haldane, Yano and Koga, Aiba et al., Teissier and Webb models. Between the five inhibition models, the Monodmodel was found to give the best fit. Therefore, the biokinetic constants estimated using these models showed good potential of the Acinetobacter baumannii and the possibility of using it in bioremediation of phenol waste effluents. The results indicatedthat in 48 hrs of incubation the bacterium was able to reduce the phenol concentrations to below detection limits. Outcomes of this study offer a useful guideline in evaluating potential phenol degraders from the environment.
机译:分离和测试苯酚降解苯酚的肺杆菌。该细菌具有高酚类降解活性和对苯酚的高耐受性。在液体培养基中在用苯酚作为单个基底进行生物冻结测定。采用不同浓度的苯酚样品从125mg /升至1000mg /点燃的观察结果。在水分培养中使用(125-1000)Mg / L的浓度范围(125-1000)Mg / L作为限制基板的分批培养物中研究了本质上的病原体肺病的生物修复潜力。研究了初始酚浓度对降解过程的影响。酚在不同初始酚浓度的不同培养时间中完全降解。将初始酚浓度从125mg / L增加到1000 mg / l增加,从0到48小时增加滞后阶段,并相应地将降解过程从84小时延长到354小时。由于初始酚浓度增加,生物学率降低。拟合数据进入Monod动力学模型,显示出苯酚的抑制作用。估计了动力学参数。RSmax降低,Ks随着较高浓度的苯酚而增加。已发现RSMAX是初始酚浓度的强功能。培养基洗涤底物抑制动力学和特定的酚类消费率适用于卤代,yano和Koga,Aiba等人。,Teissier和Webb模型。在五种抑制模型之间,发现蒙特模型给出了最合适的。因此,使用这些模型估计的生物血管血管常数显示出良好的鲍曼杆菌的潜力以及在酚废出水的生物修复中使用它的可能性。结果表明,48小时的孵育中的细菌能够将苯酚浓度降低到低于检测限。本研究结果提供了一种评估来自环境的潜在酚类降解的有用指导性。

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