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Angewandte Chemie | 2011

Tuning a P450 Enzyme for Methane Oxidation

Felipe E. Zilly; Juan Pablo Acevedo; Wojciech Augustyniak; Alfred Deege; Ulrich Häusig; Manfred T. Reetz

Cytochrome P450 (CYP) enzymes are heme-dependent monooxygenases that catalyze the oxidation of C H bonds of endogenous and exogenous organic compounds with formation of the respective alcohols. The mechanism involves the intermediacy of a high-spin oxyferryl porphyrin radical cation which abstracts a hydrogen atom from the substrate, and the short-lived alkyl radical then undergoes C Obond formation. The binding pockets of CYPs are relatively large, therefore small compounds do not have a statistically high enough probability of being properly oriented near the oxyferryl moiety for rapid oxidation to occur; additionally there are other effects that slow down or prevent catalysis. A notorious challenge is the oxidation of methane to methanol by chemical catalysis or using enzymes of the type methane monooxygenases (MMOs). It is not only the smallest alkane, but also has the strongest C H bond (104 kcalmol ). Although CYPs represent a superfamily of monooxygenases, none have been shown to accept methane, whereas MMOs are complex enzymes (many membrane bound) that have not been expressed in heterologous hosts in any significant quantities, among other problems. Herein we show that chemical tuning of a CYP, which is based on guest/host activation using perfluoro carboxylic acids as chemically inert guests, activates the enzyme for oxidation of not only medium-sized alkanes such as n-hexane, but also of small gaseous molecules such as propane and even methane as the ultimate challenge. In the present study we chose, for practical reasons, the enzyme P450 BM3 (CYP102A1) from Bacillus megaterium, which is a self-sufficient fusion protein composed of a P450 monooxygenase and an NADPH diflavin reductase. Several crystal structures of this CYP harboring a fatty acid or fatty acid derived inhibitors, as well in the absence of such compounds have been published. To engineer mutants of P450 BM3 and of other CYPs for enhanced activity and selectivity toward a variety of different compounds, including such difficult substrates as small alkanes, rational design as well as directed evolution have proven to be successful to some extent. For example, P450 BM3 variants characterized by numerous point mutations were obtained in extensive laboratory evolution, and showed for the first time notable activity toward propane by formation of the respective alcohols (2-propanol/1-propanol= 9:1); however, the ethane to ethanol conversion remains problematic and methane oxidation has not been achieved to date. Higher activity in ethane oxidation was accomplished using mutants of P450cam, but here again methane oxidation was not reported. Our chemical approach involves a chemically inert compound that serves as a guest in the binding pocket of P450 BM3, thereby filling the space and reducing the translational freedom of small alkanes or of any other substrate. On the basis of previous reports involving CYPs harboring various substrates, such guest/host interactions can be expected to induce other modes of activation effects as well, specifically water displacement at the Fe/heme site accompanied by a change in the electronic state from the inactive low-spin state to the catalytically active high-spin states. Moreover, many studies have shown that P450 enzymes and mutants thereof can harbor two different substrates simultaneously, thus leading to cooperative effects; one example is lauric acid and palmitic acid in which cooperativity has been demonstrated by isotope labeling experiments. In yet another study regarding the metabolism of bilirubin, the addition of lauric acid or the perfluorinated analogue was reported to facilitate NADPH oxidation and substrate degradation, a finding that has implications for the treatment of jaundice, uroporphyria, and possibly cancer. It has also been shown for the case of a distantly related H2O2dependent P450 enzyme that its peroxidase activity can be influenced by the addition of fatty acids, wherein increased or decreased activity is observed depending upon their chain length. In our endeavor we were guided by the binding mode of the natural substrates, fatty acids, of P450 BM3. The binding includes H-bonds originating from their carboxy function and residues Arg 47 and Tyr 51, as well as hydrophobic interactions. The use of perfluoro carboxylic acids such as 1a–h as chemically inert, yet activating guests was therefore envisioned, because perfluoro alkyl groups are known to be resistant to oxidation while having a hydrophobic character. Moreover, it is known that a CF3 residue is sterically comparable to a CH(CH3)2 group, [11a] which means that a perfluoro fatty acid fills much more space in a P450 binding pocket than a traditional fatty acid, and can additionally induce the crucial low-spin to high-spin conversion of Fe/heme. In exploratory studies, the oxidation of n-octane and n-hexane as well as isomers thereof was studied using P450 [*] Dr. F. E. Zilly, Dr. J. P. Acevedo, Dr. W. Augustyniak, A. Deege, U. W. H usig, Prof. M. T. Reetz Max-Planck-Institut f r Kohlenforschung Kaiser-Wilhelm-Platz 1, 45470 M lheim an der Ruhr (Germany) [email protected]


Catalysis Today | 2001

A GC-based method for high-throughput screening of enantioselective catalysts

Manfred T. Reetz; Klaus M. Kühling; Stephanie Wilensek; H. Husmann; Ulrich Häusig; Marcus Hermes

By combining two gas chromatography instruments (each containing a column with a chiral stationary phase) with the proper robotics and software, it is possible to construct an instrumental configuration which makes possible high-throughput screening of the enantioselectivity of a given catalytic reaction. As an example, the acylation-based catalytic kinetic resolution of racemic 2-phenyl-1-propanol catalyzed by mutant lipases can be about assayed, 700 exact E- and ee-determinations being possible per day. The method is, therefore, of interest in the directed evolution of enantioselective enzymes and/or in the combinatorial search for asymmetric transition metal catalysts.


Chromatographia | 1984

Sampling onto capillary columns. Difficulties with various types of samples a simple accessory to split injectors for avoidance of discrimination

G. Schomburg; Ulrich Häusig; H. Husmann; H. Behlau

SummaryThe quantitation problems arising by discrimination at split sampling onto capillary columns due to selective vaporization from the syringe needle after extrusion of the adjusted volume of the liquid sample into the vaporization chamber and/or due to malfunction of the splitting itself can be avoided by a simple accessory to the common injector constructions in order to arrange for cooling of the entire syringe needle except the tip. It could be proved that the discrimination which is usually observed does not originate from the splitting itself, if the temperature of the split region is not changed appreciably during the sampling procedure.


Analytica Chimica Acta | 1983

Colachrom, a command language for chromatographic data processing

Engelbert Ziegler; Bruno Weimann; Inamaria Wronka; G. Schomburg; Ulrich Häusig

Abstract A command language for the interactive computer processing of chromatograms is described. Report data files, resulting from a peak evaluation program, are processed with single-line commands. Reference peaks for quantitative evaluation or for retention index calculations can be specified, compound names or response factors be assigned, etc. Customer-specific reports can be generated. Several commands operate on the unreduced digitized chromatograms, e.g., repeat peak evaluation with modified peak search parameters or with a user-corrected baseline. Commands can be combined into procedures for semi-automatic processing of series of chromatograms. Various forms of interactive graphical presentations supplement the command language.


Angewandte Chemie | 2007

Microfluidic glass chips with an integrated nanospray emitter for coupling to a mass spectrometer

Peter Hoffmann; Ulrich Häusig; Philipp Schulze; Detlev Belder


Hrc-journal of High Resolution Chromatography | 1990

Prodution of windows in fused silica capillaries for in-column detection of UV-absorption or fluorescence in capillary electrophoresis or HPLC

Jürgen A. Lux; Ulrich Häusig; G. Schomburg


Hrc-journal of High Resolution Chromatography | 1985

Quantitation in capillary gas chromatography with emphasis on the problems of sample introduction

G. Schomburg; Ulrich Häusig; H. Husmann


Hrc-journal of High Resolution Chromatography | 1985

Application of the “cooled needle” technique to split and splitless sampling onto capillary columns

G. Schomburg; Ulrich Häusig


Hrc-journal of High Resolution Chromatography | 1989

Quantitation in miniaturized GC and SFC systems

G. Schomburg; H. Behlau; Ulrich Häusig; B. Hoening; W. Roeder


Angewandte Chemie | 2007

Mikrofluidische Glas-Chips mit integriertem Nanospray-Emitter zur Kopplung mit der Massenspektrometrie†

Peter Hoffmann; Ulrich Häusig; Philipp Schulze; Detlev Belder

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Peter Hoffmann

Potsdam Institute for Climate Impact Research

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