Choi Dong W, Antholine William E, Do Young S, Semrau Jeremy D, Kisting Clint J, Kunz Ryan C, Campbell Damon, Rao Vinay, Hartsel Scott C, DiSpirito Alan A
Department of Biochemistry, Biophysics and Molecular Biology, 4164 Molecular Biology Building, Iowa State University, Ames, IA 50011-3211, USA.
Department of Biophysics, Medical College of Wisconsin, Milwaukee, WI 53226, USA.
Microbiology (Reading). 2005 Oct;151(Pt 10):3417-3426. doi: 10.1099/mic.0.28169-0.
Improvements in the purification of methanobactin (mb) from either Methylosinus trichosporium OB3b(T) or Methylococcus capsulatus Bath resulted in preparations that stimulated methane-oxidation activity in both whole-cell and cell-free fractions of Methylococcus capsulatus Bath expressing the membrane-associated methane monooxygenase (pMMO). By using washed membrane factions with pMMO activities in the 290 nmol propylene oxidized min(-1) (mg protein)(-1) range, activities approaching 400 nmol propylene oxidized min(-1) (mg protein)(-1) were commonly observed following addition of copper-containing mb (Cu-mb), which represented 50-75 % of the total whole-cell activity. The stimulation of methane-oxidation activity by Cu-mb was similar to or greater than that observed with equimolar concentrations of Cu(II), without the inhibitory effects observed with high copper concentrations. Stimulation of pMMO activity was not observed with copper-free mb, nor was it observed when the copper-to-mb ratio was <0.5 Cu atoms per mb. The electron paramagnetic resonance (EPR) spectra of mb differed depending on the copper-to-mb ratio. At copper-to-mb ratios of <0.4 Cu(II) per mb, Cu(II) addition to mb showed an initial coordination by both sulfur and nitrogen, followed by reduction to Cu(I) in <2 min. At Cu(II)-to-mb ratios between 0.4 and 0.9 Cu(II) per mb, the intensity of the Cu(II) signal in EPR spectra was more representative of the Cu(II) added and indicated more nitrogen coordination. The EPR spectral properties of mb and pMMO were also examined in the washed membrane fraction following the addition of Cu(II), mb and Cu-mb in the presence or absence of reductants (NADH or duroquinol) and substrates (CH4 and/or O2). The results indicated that Cu-mb increased electron flow to the pMMO, increased the free radical formed following the addition of O2 and decreased the residual free radical following the addition of O2 plus CH4. The increase in pMMO activity and EPR spectral changes to the pMMO following Cu-mb addition represent the first positive evidence of interactions between the pMMO and Cu-mb.
从 trichosporium OB3b(T)甲基弯曲菌或荚膜甲基球菌中提纯甲烷菌素(mb)的方法得到了改进,所制备的产物能够刺激表达膜相关甲烷单加氧酶(pMMO)的荚膜甲基球菌全细胞部分和无细胞部分的甲烷氧化活性。使用pMMO活性在290 nmol丙烯氧化min⁻¹(mg蛋白)⁻¹范围内的洗涤过的膜部分,加入含铜mb(Cu-mb)后通常可观察到活性接近400 nmol丙烯氧化min⁻¹(mg蛋白)⁻¹,这占全细胞总活性的50 - 75%。Cu-mb对甲烷氧化活性的刺激作用与等摩尔浓度的Cu(II)相似或更强,且没有高铜浓度时观察到的抑制作用。无铜mb未观察到对pMMO活性的刺激作用,当铜与mb的比例小于每mb 0.5个铜原子时也未观察到。mb的电子顺磁共振(EPR)光谱因铜与mb的比例不同而有所差异。在每mb铜与mb的比例小于0.4 Cu(II)时,向mb中添加Cu(II)显示最初由硫和氮配位,随后在不到2分钟内还原为Cu(I)。在每mb铜与mb的比例介于0.4和0.9 Cu(II)之间时,EPR光谱中Cu(II)信号的强度更能代表添加的Cu(II),且表明更多的氮配位。在添加Cu(II)、mb和Cu-mb后,在有或没有还原剂(NADH或杜醌)和底物(CH₄和/或O₂)存在的情况下,还对洗涤过的膜部分中mb和pMMO的EPR光谱特性进行了研究。结果表明,Cu-mb增加了向pMMO的电子流,增加了添加O₂后形成的自由基,并减少了添加O₂加CH₄后残留的自由基。添加Cu-mb后pMMO活性的增加以及pMMO的EPR光谱变化代表了pMMO与Cu-mb之间相互作用的首个确凿证据。