Cort Todd L, Song Myoung-Suk, Bielefeldt Angela R
Cameron-Cole, LLC, Boulder, CO 80301, USA.
Water Res. 2002 Mar;36(5):1253-61. doi: 10.1016/s0043-1354(01)00320-7.
Several potential mechanisms of surfactant-induced inhibition of pentachlorophenol (PCP) biodegradation were tested using a pure bacterial culture of Sphingomonas chlorophenolicum sp. Strain RA2. PCP degradation, glucose degradation, and oxygen uptake during endogenous conditions and during glucose degradation were measured for batch systems in the presence of the nonionic surfactant Tergitol NP-10 (TNP10). TNP10 did not exert toxicity on RA2 as measured by dissolved oxygen uptake rates under endogenous conditions and glucose biodegradation rates. TNPIO reduced the substrate inhibition effect of PCP at high PCP concentrations, resulting in faster PCP degradation rates at higher concentrations of TNP10. Calculations of a micelle partition coefficient (Kmic) show that PCP degradation rates in the presence of surfactant can be explained by accounting for the amount of PCP available to the cell in the aqueous solution. A model is discussed based on these results where PCP is sequestered into micelles at high TNP10 concentrations to become less available to the bacterial cell and resulting in observed inhibition. Under substrate toxicity conditions, the same mechanism serves to increase the rate of PCP biodegradation by reducing aqueous PCP concentrations to less toxic levels.
利用嗜氯酚鞘氨醇单胞菌菌株RA2的纯细菌培养物,测试了表面活性剂诱导抑制五氯酚(PCP)生物降解的几种潜在机制。在非离子表面活性剂Tergitol NP - 10(TNP10)存在的情况下,针对分批系统测量了内源性条件下以及葡萄糖降解过程中的PCP降解、葡萄糖降解和氧气摄取情况。以内源性条件下的溶解氧摄取速率和葡萄糖生物降解速率衡量,TNP10对RA2未产生毒性。TNPIO降低了高PCP浓度下PCP的底物抑制效应,在较高浓度的TNP10存在时导致更快的PCP降解速率。胶束分配系数(Kmic)的计算表明,表面活性剂存在时PCP的降解速率可以通过考虑水溶液中细胞可利用的PCP量来解释。基于这些结果讨论了一个模型,在该模型中,高TNP10浓度下PCP被隔离到胶束中,从而使细菌细胞可利用的PCP减少,导致观察到抑制现象。在底物毒性条件下,相同机制通过将水溶液中PCP浓度降低到较低毒性水平来提高PCP生物降解速率。