陳長謙臺灣大學：化學研究所王琢堅Wang, Vincent Cho-ChienVincent Cho-ChienWang2007-11-262018-07-102007-11-262018-07-102005http://ntur.lib.ntu.edu.tw//handle/246246/51908Potentiometric titrations of the copper centers in the particulate methane monooxygenase (pMMO) from Methylococcus capsulatus (Bath) are described. The reduction potentials of the various copper centers were measured by poising the enzyme in pMMO-enriched membranes in the presence of different redox mediators in an electrochemical cell, and quickly freezing the sample to record their low temperature EPR signals. Measurements of the low temperature EPR intensities of the type 2 sites and trinuclear Cu(II) centers yielded [Cu(I)]/[Cu(II)] for the various copper centers at the various different potentials, and the mid-point potentials were determined from the Nernst equation. The measurements were performed on two different forms of the enzyme in pMMO-enriched membranes: (i) the enzyme as isolated aerobically, but in the absence of hydrocarbon substrate; and (ii) the same preparation oxidized under air in the presence of acetylene or other hydrocarbon substrates. While the E-cluster copper sites exhibited essentially the same high reduction potential of +490 mV, substantially different results were obtained for the redox behavior of the C-cluster copper ions between the two forms. The reduction potentials of the oxidized C-cluster copper sites observed in the EPR were found to be substantially lower compared to that of the E-clusters. Accordingly, the redox potential of the oxidized bis(μ–oxo)dicopper(III) and bis(μ–peroxo)dicopper (II) dimer associated with the isolated type 2 site of the same cluster must be considerably higher than +490 mV, and there must be a kinetic barrier for transfer of electrons from the E-clusters to this site. This “splitting” of the redox potential of the trinuclear copper cluster is artifactual of the non-physiological state of enzyme created from the oxidation of the six copper ions by eight oxidizing equivalents from two dioxygen molecules. When the enzyme is turning over in the presence of hydrocarbon substrate, the dioxygen chemistry is tightly linked to the hydroxylation chemistry to achieve kinetic competence, and the redox potentials of the C-cluster copper ions were found to be substantially higher. The results of the present study add a significant chapter to our understanding of the structure and function of pMMO. First, the potentiometric titrations confirmed without any further question the existence of C-cluster and E-cluster copper ions, the number of distinct C-clusters, as well as the functional role they play in the methane hydroxylation chemistry, as the various copper centers are distinguished by distinct redox behaviors in the EPR, as manifested by their different appearance in the EPR spectrum at different potentials. Second, the different redox behavior of the C-clusters copper ions between the “as-isolated” enzyme and during turnover in the presence of hydrocarbon substrate has led to important insights into the details of how electron transport, dioxygen chemistry and hydrocarbon oxidation are linked in this complex system.Acknowledgement (Chinese) II Abstract Chinese) IV Abstract (Englich) V Abbreviations VII Chapter 1 Introduction 1.0 Preface and Methanotrophs 2 1.1 The MMO System: 1.1.1 sMMO 5 1.1.2 pMMO 5 1.2 Copper proteins 1.2.1 Proteins 13 1.2.2 Spectroscopic definition of copper ions 13 1.3 Hydroxylation of alkanes by pMMO. Unusual regioselectivity and stereoselectivity 1.3.1 C and E clusters 17 1.3.2 Mechanism of oxo transfer in pMMO 18 1.3.3 Methane hydroxylation is linked to the oxidase reaction in pMMO 19 1.4 Aim of this dissertation 22 1.5 References 24 Chapter 2 Materials and Methods 2.1 Chemical reagents 28 2.2 Culturing of Methylococcus capsulatus (Bath) 29 2.3 Isolation and purification of “as-isolated” pMMO from pMMO-enriched membranes 30 2.4 Protein analysis and activity assays 31 2.5 Monitoring the redox potentials of the copper clusters in pMMO 2.5.1 Standard redox potentials of redox mediators used 32 2.5.2 Instrumentation used in the measurements of redox potentials 33 2.6 Potentiometric titrations 2.6.1 “As-isolated” membranes 34 2.6.2 The addition of exogenous ligands 35 2.7 Redox potentials of various reductants and oxidants used in the potentiometric titrations 36 2.8 EPR measurements 36 2.9 X-ray absorption spectroscopy 36 2.10 References 37 Chapter 3 Theory 3.1 Electron Paramagnetic Resonance 3.1.1 Zeeman effect 40 3.1.2 EPR transitions 41 3.1.3 Hyperfine Interactions 45 3.1.4 Origin of nuclear hyperfine interactions 45 3.2 Zero-field splittings 47 3.3 Exchange interactions 47 3.4 EPR signal of type 2 copper 48 3.5 EPR signal of a trinuclear copper cluster 49 3.6 X-ray absorption spectroscopy 54 3.7 References 56 Chapter 4 Results and Discussion 4.1 pMMO-enriched membranes 58 4.2 Different redox potential for the C-cluster copper ions between active and non-active pMMO 58 4.3 The effects of mediators on pMMO in the absence of hydrocarbon substrate 61 4.4 Potentiometric titration of the copper ions in the C-clusters and E-clusters in “as-isolated” pMMO-enriched membranes 65 4.5 Potentiometric titration of fully oxidated pMMO in the presence of hydrocarbon or acetylene 71 4.6 Interaction between exogenous ligands and pMMO 79 4.7 References 82 Chapter 5 Conclusions 84 Appendix I Structure of mediators 873274037 bytesapplication/pdfen-US微粒體甲烷單氧化酵素電子自旋光譜pMMOmonooxygenasepotentiometric titrationEPRthesishttp://ntur.lib.ntu.edu.tw/bitstream/246246/51908/1/ntu-94-R92223037-1.pdf