Departments of Crop and Soil Sciences and of Microbiology and Public Health, Michigan State University, East Lansing, Michigan 48824.
Appl Environ Microbiol. 1983 May;45(5):1466-73. doi: 10.1128/aem.45.5.1466-1473.1983.
The kinetic parameters associated with the microbial dehalogenation of 3-chlorobenzoate, 3,5-dichlorobenzoate, and 4-amino-3,5-dichlorobenzoate were measured in anoxic sediment slurries and in an enriched methanogenic culture grown on 3-chlorobenzoate. The initial dehalogenation of the substrates exhibited Michaelis-Menten kinetics. The apparent K(m) values for the above substrates ranged from 30 to 67 muM. The pattern of degradation, however, was unusual. The enrichment culture accumulated partially dehalogenated intermediates to 72 and 98% of that possible when incubated with either 3,5-dichloro- or 4-amino-3,5-dichlorobenzoate, respectively, but did not accumulate significant amounts of benzoate when 3-chlorobenzoate was the sole carbon and energy source. The accumulated intermediates were rapidly metabolized only after the parent substrate concentrations were nearly depleted (<5 muM). A sequential Michaelis-Menten model was developed to account for the observed pattern of biodegradation. Using this model, we found that relative differences in the K(m) and V(max) parameters for substrate and intermediate dehalogenations alone were insufficient to explain the transitory accumulation of intermediates. However, by inserting a competitive inhibition term, with the primary substrate as the inhibitor, the observed pattern of degradation was simulated. Apparently, the dichlorinated substrates competitively inhibit the dehalogenation of the monochlorinated substrates. Similar kinetic patterns were noted for sediments, although the rates were slower than in the enrichment culture.
在缺氧沉积物悬浮液中和在以 3-氯苯甲酸为唯一碳源和能源的富集产甲烷培养物中,测量了与微生物脱卤化 3-氯苯甲酸、3,5-二氯苯甲酸和 4-氨基-3,5-二氯苯甲酸相关的动力学参数。底物的初始脱卤化表现出米氏动力学。上述底物的表观 K(m) 值范围为 30 至 67 μM。然而,降解模式是不寻常的。富集培养物将部分脱卤化中间体积累到 72%和 98%,分别与 3,5-二氯苯甲酸或 4-氨基-3,5-二氯苯甲酸孵育时可能达到的水平,但当 3-氯苯甲酸是唯一的碳源和能源时,不会积累大量的苯甲酸。只有在母体底物浓度几乎耗尽(<5 μM)后,积累的中间体才会迅速代谢。开发了一个顺序米氏酶动力学模型来解释观察到的生物降解模式。使用该模型,我们发现,仅考虑底物和中间体脱卤化的 K(m) 和 V(max) 参数的相对差异不足以解释中间体的暂态积累。然而,通过插入一个竞争性抑制项,以主要底物作为抑制剂,可以模拟观察到的降解模式。显然,二氯代底物竞争性地抑制一氯代底物的脱卤化。在沉积物中也注意到了类似的动力学模式,尽管速率比富集培养物慢。