Yu Seungho, Dolan Mark E, Semprini Lewis
Department of Civil, Construction, and Environmental Engineering, Oregon State University, Corvallis, Oregon 97331, USA.
Environ Sci Technol. 2005 Jan 1;39(1):195-205.
Kinetic studies with two different anaerobic mixed cultures (the PM and the EV cultures) were conducted to evaluate inhibition between chlorinated ethylenes. The more chlorinated ethylenes inhibited the reductive dechlorination of the less chlorinated ethylenes, while the less chlorinated ethylenes weakly inhibited the dechlorination of the more chlorinated ethylenes. Tetrachloroethylene (PCE) inhibited reductive trichloroethylene (TCE) dechlorination but not cis-dichloroethylene (c-DCE) dechlorination, while TCE strongly inhibited c-DCE and VC dechlorination. c-DCE also inhibited vinyl chloride (VC) transformation to ethylene (ETH). When a competitive inhibition model was applied, the inhibition constant (K(I)) for the more chlorinated ethylene was comparable to its respective Michaelis-Menten half-velocity coefficient, K(S). Model simulations using independently derived kinetic parameters matched the experimental results well. k(max) and K(S) values required for model simulations of anaerobic dechlorination reactions were obtained using a multiple equilibration method conducted in a single reactor. The method provided precise kinetic values for each step of the dechlorination process. The greatest difference in kinetic parameters was for the VC transformation step. VC was transformed more slowly by the PM culture (k(max) and K(S) values of 2.4+/-0.4 micromol/mg of protein/day and 602+/-7 microM, respectively) compared to the EV culture (8.1+/-0.9 micromol/mg of protein/day and 62.6+/-2.4 microM). Experimental results and model simulations both illustrate how low K(S) values corresponded to efficient reductive dechlorination for the more highly chlorinated ethylenes but caused strong inhibition of the transformation of the less chlorinated products. Thus, obtaining accurate K(S) values is important for modeling both transformation rates of parent compounds and their inhibition on daughter product transformation.
采用两种不同的厌氧混合培养物(PM和EV培养物)进行动力学研究,以评估氯乙烯之间的抑制作用。多氯代乙烯抑制少氯代乙烯的还原脱氯,而少氯代乙烯对多氯代乙烯的脱氯有较弱的抑制作用。四氯乙烯(PCE)抑制三氯乙烯(TCE)的还原脱氯,但不抑制顺式二氯乙烯(c-DCE)的脱氯,而TCE强烈抑制c-DCE和氯乙烯(VC)的脱氯。c-DCE也抑制氯乙烯(VC)向乙烯(ETH)的转化。当应用竞争抑制模型时,多氯代乙烯的抑制常数(K(I))与其各自的米氏半速度系数K(S)相当。使用独立推导的动力学参数进行的模型模拟与实验结果吻合良好。厌氧脱氯反应模型模拟所需的k(max)和K(S)值通过在单个反应器中进行的多重平衡法获得。该方法为脱氯过程的每个步骤提供了精确的动力学值。动力学参数差异最大的是VC转化步骤。与EV培养物(8.1±0.9 μmol/mg蛋白质/天和62.6±2.4 μM)相比,PM培养物中VC的转化较慢(k(max)和K(S)值分别为2.4±0.4 μmol/mg蛋白质/天和602±7 μM)。实验结果和模型模拟均表明,低K(S)值对应于多氯代乙烯的高效还原脱氯,但会强烈抑制少氯代产物的转化。因此,获得准确的K(S)值对于模拟母体化合物的转化率及其对产物转化的抑制作用非常重要。