Department of Civil and Environmental Engineering, The University of Michigan, Ann Arbor, Michigan 48109-2125.
Appl Environ Microbiol. 1998 Mar;64(3):1106-14. doi: 10.1128/AEM.64.3.1106-1114.1998.
Whole-cell assays of methane and trichloroethylene (TCE) consumption have been performed on Methylosinus trichosporium OB3b expressing particulate methane monooxygenase (pMMO). From these assays it is apparent that varying the growth concentration of copper causes a change in the kinetics of methane and TCE degradation. For M. trichosporium OB3b, increasing the copper growth concentration from 2.5 to 20 muM caused the maximal degradation rate of methane (V(max)) to decrease from 300 to 82 nmol of methane/min/mg of protein. The methane concentration at half the maximal degradation rate (K(s)) also decreased from 62 to 8.3 muM. The pseudo-first-order rate constant for methane, V(max)/K(s), doubled from 4.9 x 10 to 9.9 x 10 liters/min/mg of protein, however, as the growth concentration of copper increased from 2.5 to 20 muM. TCE degradation by M. trichosporium OB3b was also examined with varying copper and formate concentrations. M. trichosporium OB3b grown with 2.5 muM copper was unable to degrade TCE in both the absence and presence of an exogenous source of reducing equivalents in the form of formate. Cells grown with 20 muM copper, however, were able to degrade TCE regardless of whether formate was provided. Without formate the V(max) for TCE was 2.5 nmol/min/mg of protein, while providing formate increased the V(max) to 4.1 nmol/min/mg of protein. The affinity for TCE also increased with increasing copper, as seen by a change in K(s) from 36 to 7.9 muM. V(max)/K(s) for TCE degradation by pMMO also increased from 6.9 x 10 to 5.2 x 10 liters/min/mg of protein with the addition of formate. From these whole-cell studies it is apparent that the amount of copper available is critical in determining the oxidation of substrates in methanotrophs that are expressing only pMMO.
已在表达颗粒态甲烷单加氧酶(pMMO)的甲基孢囊菌 OB3b 上进行了甲烷和三氯乙烯(TCE)消耗的全细胞测定。从这些测定中可以明显看出,铜的生长浓度的变化会导致甲烷和 TCE 降解的动力学发生变化。对于 M. trichosporium OB3b,将铜的生长浓度从 2.5 增加到 20 μM 会导致甲烷的最大降解速率(V(max))从 300 减少到 82 nmol 的甲烷/min/mg 的蛋白质。甲烷的半最大降解速率(K(s))也从 62 减少到 8.3 μM。甲烷的拟一级速率常数,V(max)/K(s),从 4.9 x 10 增加到 9.9 x 10 升/min/mg 的蛋白质,然而,随着铜的生长浓度从 2.5 增加到 20 μM。还研究了不同铜和甲酸盐浓度下 M. trichosporium OB3b 的 TCE 降解。在没有和存在外源还原当量(甲酸形式)的情况下,用 2.5 μM 铜培养的 M. trichosporium OB3b 都无法降解 TCE。然而,用 20 μM 铜培养的细胞无论是否提供甲酸盐都能够降解 TCE。没有甲酸盐时,TCE 的 V(max)为 2.5 nmol/min/mg 的蛋白质,而提供甲酸盐时,V(max)增加到 4.1 nmol/min/mg 的蛋白质。随着铜浓度的增加,TCE 的亲和力也增加,K(s)从 36 变为 7.9 μM。在添加甲酸盐的情况下,pMMO 降解 TCE 的 V(max)/K(s)也从 6.9 x 10 增加到 5.2 x 10 升/min/mg 的蛋白质。从这些全细胞研究中可以明显看出,可用铜的量对于确定仅表达 pMMO 的甲烷营养菌中底物的氧化是至关重要的。