Bailey Lucas J, Elsen Nathaniel L, Pierce Brad S, Fox Brian G
Department of Biochemistry, University of Wisconsin, 433 Babcock Drive, Madison, WI 53706-1544, USA.
Protein Expr Purif. 2008 Jan;57(1):9-16. doi: 10.1016/j.pep.2007.09.007. Epub 2007 Sep 19.
Toluene 4-monooxygenase (T4MO) is a member of the bacterial multicomponent monooxygenases, an enzyme family that utilizes a soluble diiron hydroxylase to oxidize a variety of hydrocarbons as the initial step in their metabolism. The hydroxylases obtain reducing equivalents from NAD(P)H via an electron transfer chain that is initiated by an oxidoreductase containing an N-terminal ferredoxin domain and C-terminal flavin- and NAD-binding domains. T4moF, the NADH oxidoreductase of T4MO, was expressed as a soluble protein in Escherichia coli BL21(DE3) from the pUC-derived expression vector pRS205. This vector contains a lac promoter instead of a T7 promoter. A three step purification from the soluble cell lysate yielded approximately 1 mg of T4moF per gram of wet cell paste with greater than 90% purity. The purified protein contained 1 mol of FAD and 2 mol of Fe per mol of T4moF; quantitative EPR spectroscopy showed approximately 1 mol of the S=1/2 signal from the reduced [2Fe-2S] cluster per mol of T4moF. Steady state kinetic analysis of p-cresol formation activity treating T4moF as the variable substrate while all other proteins and substrates were held constant gave apparent K(M-) and apparent k(cat)-values of 0.15 microM and 3.0 s(-1), respectively. This expression system and purification allows for the recovery of the soluble oxidoreductase in yields that facilitate further biochemical and structural characterizations.
甲苯4-单加氧酶(T4MO)是细菌多组分单加氧酶家族的一员,该酶家族利用可溶性二铁羟化酶氧化多种碳氢化合物,作为其代谢的第一步。羟化酶通过由含有N端铁氧化还原蛋白结构域和C端黄素及NAD结合结构域的氧化还原酶启动的电子传递链从NAD(P)H获得还原当量。T4MO的NADH氧化还原酶T4moF在大肠杆菌BL21(DE3)中由pUC衍生的表达载体pRS205表达为可溶性蛋白。该载体含有lac启动子而非T7启动子。从可溶性细胞裂解物中进行三步纯化,每克湿细胞糊可产生约1毫克T4moF,纯度大于90%。纯化后的蛋白每摩尔T4moF含有1摩尔FAD和2摩尔Fe;定量EPR光谱显示每摩尔T4moF约有1摩尔来自还原型[2Fe-2S]簇的S=1/2信号。以T4moF为可变底物,同时保持所有其他蛋白质和底物不变,对生成对甲酚的活性进行稳态动力学分析,得到的表观K(M-)和表观k(cat)-值分别为0.15 microM和3.0 s(-1)。这种表达系统和纯化方法能够以有助于进一步进行生化和结构表征的产量回收可溶性氧化还原酶。