The present invention relates to a nucleic acid molecule encoding a polypeptide having cytochrome P450 monooxygenase activity, wherein said polypeptide comprises a reductase domain that deviates by at least one mutation from (a) the reductase domain of cytochrome P450 BM3, wherein the reductase domain of cytochrome P450 BM3 is represented by SEQ ID NO: 1 ; or (b) a reductase domain having at least 95% sequence identity to SEQ ID NO: 1 ; and wherein said mutation(s) result(s) in an increased cytochrome P450 monooxygenase activity as compared to a polypeptide comprising the reductase domain of SEQ ID NO:1 . The present invention also relates to a vector comprising the nucleic acid molecule of the invention and a host transformed with the vector. Furthermore, the invention relates to a method of producing a polypeptide comprising culturing the host of the invention as well as to a polypeptide encoded by the nucleic acid molecule of the invention or produced by the method of the invention. The present invention further relates to the use of the polypeptide of the invention in biotransformation or fine chemical synthesis, to an oiigo- or polynucleotide which specifically hybridizes to the nucleic acid molecule of the invention as well as to a composition and to a kit.

In this specification, a number of documents including patent applications and manufacturer's manuals is cited. The disclosure of these documents, while not considered relevant for the patentability of this invention, is herewith incorporated by reference in its entirety. More specifically, all referenced documents are incorporated by reference to the same extent as if each individual document was specifically and individually indicated to be incorporated by

Cytochrome P450 enzymes are a group of enzymes involved in the oxidative metabolism of drugs and carcinogens as well as a high number of natural compounds such as steroids, fatty acids, prostaglandins, and leukotrienes (Porter, T.D. and Coon, M.J. (1991 ) Cytochrome P450: multiplicity of isoforms, substrates, and catalytic and regulatory mechanisms, J. Biol. Chem.266: 13469-13472). They are found throughout the phylogenetic spectrum and have been classified into about forty different families. P450 enzymes are heme-proteins with a conserved cysteine residue. Many bacteria utilize P450 to grow on particular carbon sources or in the biosynthesis of secondary metabolites. The monooxygenase P450 BM-3 is a cytochrome P450 enzyme originating from Bacillus megaterium -the product of the CYP 102 gene- and shows a high sequence homology with P450 enzymes from mammals (Boddupalli, S. S. et al., 1990, Fatty acid monooxygenation by cytochrome P-450 BM-3, J. Biol. Chem. 265, 4233-4239). Due to this similarity, P450 BM-3 represents a suitable model for mammalian P450 enzymes. P450 BM-3 is a 1 19 kDa water- soluble enzyme and its catalytic activity is one of the highest among all known P450 enzymes. Furthermore, cytochrome P-450 BM-3 is a catalytically self-sufficient fatty acid hydroxylase which monooxygenates saturated and unsaturated fatty acids, alcohols, and amides. Conversion of long chain alcohols and amines has also been reported as a natural activity of P450 BM-3. The enzyme converts lauric, myristic, and palmitic acids to omega-1 , omega-2, and omega-3 hydroxy analogues. The catalytic activity is dependent on the chain length of the fatty acid, with an optimum chain length of 14 to 16 carbon atoms.

The P450 BM-3 protein consists of 1048 amino acids and has two domains: a first domain which contains heme and is P-450-oxygenase-like (471 aa; also referred to herein as oxygenase domain) and a second domain which contains FAD and FMN and is P-450 reductase-like (577 aa; also referred to herein as reductase domain). Both domains are located on a single polypeptide chain, separated by a trypsin cleavage site (Ruettinger et al. (1989), Coding nucleotide, 5 ^' -Regulatory, and Deduced Amino Acid Sequences of P-450 BM- 3, a Single Peptide Cytochrome P-450: NADPH-P-450 reductase from Bacillus megaterium, J. Biol. Chem. 264, 19: 10987-10995). Attempts to crystallize the full length protein were unsuccessful, most likely due to the presence of a highly flexible "hinge" region connecting the heme and the reductase domains of the protein. However, the structure of the heme- as well as the heme/FMN-binding complex have been solved. These structures enabled the rational investigation of the structure/function relationship in P450 BM3 by identifying key residues involved in substrate binding and catalysis as well as electron transfer from NADPH (Ravichandran, K.G., Boddupalli, S.S., Hasermann, C.A., Peterson, J.A. and Deisenhofer, J. (1993), Crystal structure of hemoprotein domain of P450 BM-3, a prototype for microsomal P450's. Science 261 , 731 -736; Sevrioukova. I.F., Li, H., Zhang, H.. Peterson, J.A. and Poulos, T.L. (1999) Structure of a cytochrome P450-redox partner electron-transfer complex. Proc Natl Acad Sci USA 96: 1863-1868).

In the literature a number of variants and mutations of P450 BM3 have been described that aim at changing the substrate specificity and the products of hydroxylation. Notably, however, these mutations were predominantly located in the heme domain of the enzyme, whereas the reductase domain was mostly wild type. The heme domain of P450 BM3 consists of a and β sub-domains. The heme in the active site is positioned within a long hydrophobic substrate binding channel formed predominantly by β sub-domains. The heme porphyrin ring is bound to the rest of the polypeptide chain through the Cys400 residue, which is well conserved among other P450s. So far, a number of different residues have been identified as having a possible effect on substrate-binding or catalysis. For example, Arg47 is thought to interact with carboxyl groups of fatty acids, thus stabilizing the negative charge of the substrate through ionic interaction while Phe87 is thought to have an important role in substrate binding and region-selectivity of oxidation. Further, Arg 471 was found to improve the stability of P450 BM3 toward co-solvents such as DMSO (Wong, T.S., Arnold, F.H., and Schwaneberg, U., 2004, Laboratory evolution of cytochrome P450 BM-3 monooxygenase for organic co- solvents. Biotechnology and Bioengineering 85, 3: 351 -358). Amongst others, these residues have an important role on substrate recognition and conversion (Noble, M.A., Miles, C.S., Chapman, S.K., Lysek, D.A., MacKay, A.C., Reid, G.A., Hanzlik, R.P. and Munro, A.W. (1999) Roles of key active-site residues in flavocytochrome P450 BM3. Biochem J. 339: 371 -379).

Further publications that have described mutations in the heme domain are e.g. Whitehouse et al. (2009), A highly active single-mutation variant of P450 BM3 (CYP102A1 ), Chem. Biochem., 10(10): 1654-6 and Girvan, HM. (2009), Novel haem co-ordination variants of flavocytochrome P450 BM3, Biochem. J. 417(1 ): 65-76. Furthermore, also a number of patents/patent applications disclose mutations in the heme domain and their effect on enzyme characteristics (see e.g. US 7691616, US 776768, US 7704715, EP 1 196603 B1 , EP 1 196545 B1 , EP 1 196605 B1 , US 7531335, US 7524664, US 7226768, US 2009/026431 1 A1 , WO 2003/008563 A2). One example of engineering both the heme and the reductase domains of cytochrome P450 monooxygenase is described in WO 2008/1 15844 A2, which discloses chimeric P450 holoenzymes obtained by site-directed recombination. Chimeric enzymes comprising rearranged segments of the heme- and the reductase domains were recombinantly expressed in host cells and the enzymes investigated for improved monooxygenase activity as well as different substrate specificity of the chimeric polypeptides as compared to the wild- type polypeptide, showing that a whole set of novel enzymes were generated by this procedure.

Mutations in the reductase domain - or in both the heme and the reductase domain - are rarely described in the art. The reductase domain was described to be mutated in two positions - amino acids 494 and 1024 - in US 7226768 and WO 2003/008563 A2. With regard to these mutations in the reductase domain, the effect disclosed is a higher organic solvent resistance, while mutations in the heme domain are discussed in US 7226768 and WO 2003/008563 A2 as resulting in a higher alkane/alkene-oxidation capability. Although some of the mutants disclosed in US 7226768 and WO 2003/008563 A2 are shown to have an increased activity also in the absence of co-solvents, these results were obtained for enzymes having mutations in both the heme and the reductase domain. The inventors of US 7226768 and WO 2003/008563 ascribe the improvement to the mutations in the heme domain and show a further improvement in the presence of co-solvents, which is ascribed to the mutations in the reductase domain which are believed to increase the enzyme's resistance to these solvents.

Patent applications WO 2007/129050 and US 2009/0186415 A1 disclose beneficial effects of a truncated reductase domain on the co-expressed cytochrome P450 with regard to expression and activity of cytochrome P450. WO 03/014341 describes a chimeric protein comprising the P450 BM3 reductase domain and the heme domain from a mammalian or plant cytochrome P450 useful for analysis of substrate specificities.

Despite the above described advances in the development of P450 enzymes with altered enzyme characteristics, there is still the need to provide P450 enzymes having increased enzymatic activity.

This need is addressed by the provision of the embodiments characterised in the claims. Accordingly, the present invention relates to a nucleic acid molecule encoding a polypeptide having cytochrome P450 monooxygenase activity, wherein said polypeptide comprises a reductase domain that deviates by at least one mutation from (a) the reductase domain of cytochrome P450 BM3, wherein the reductase domain of cytochrome P450 BM3 is represented by SEQ ID NO: 1 ; or (b) a reductase domain having at least 95% sequence identity to SEQ ID NO:1 ; and wherein said mutation(s) result(s) in an increased cytochrome P450 monooxygenase activity as compared to a polypeptide comprising the reductase domain of SEQ ID NO:1 .

The term "nucleic acid molecule" in accordance with the present invention includes DNA, such as cDNA or genomic DNA, and RNA. In this regard, "DNA" (deoxyribonucleic acid) means any chain or sequence of the chemical building blocks adenine (A), guanine (G), cytosine (C) and thymine (T), called nucleotide bases, that are linked together on a deoxyribose sugar backbone. DNA can have one strand of nucleotide bases, or two complementary strands which may form a double helix structure. "RNA" (ribonucleic acid) means any chain or sequence of the chemical building blocks adenine (A), guanine (G), cytosine (C) and uracil (U), called nucleotide bases, that are linked together on a ribose sugar backbone. RNA typically has one strand of nucleotide bases. Included are also single- and double-stranded hybrid molecules, i.e., DNA-DNA, DNA-RNA and RNA-RNA, wherein one of the strands encodes the mentioned polypeptide. The nucleic acid molecule may also be modified by means known in the art. Non-limiting examples of such modifications include methylation, "caps", substitution of one or more of the naturally occurring nucleotides with an analogue, and inter-nucleotide modifications such as, for example, those with uncharged linkages (e.g., methyl phosphonates, phosphotriesters, phosphoroamidates, carbamates, etc.) and with charged linkages (e.g., phosphorothioates, phosphorodithioates, etc.). Further included are nucleic acid mimicking molecules known in the art such as synthetic or semi-synthetic derivatives of DNA or RNA and mixed polymers. Such nucleic acid mimicking molecules or nucleic acid derivatives according to the invention include phosphorothioate nucleic acid, phosphoramidate nucleic acid, 2'-0-methoxyethyl ribonucleic acid, morpholino nucleic acid, hexitol nucleic acid (HNA), peptide nucleic acid (PNA) and locked nucleic acid (LNA) (see Braasch and Corey, Chem Biol 2001 , 8: 1 ). LNA is an RNA derivative in which the ribose ring is constrained by a methylene linkage between the 2'-oxygen and the 4'-carbon. Also included are nucleic acids containing modified bases, for example thio-uracil, thio-guanine and fluoro- uraci!. A nucleic acid molecule typically carries genetic information, including the information used by the cellular machinery to make polypeptides. The nucleic acid molecule of the invention may additionally comprise promoters, enhancers, response elements, signal sequences, polyadenylation sequences, introns, 5'- and 3'- non-coding regions, and the like.

The term "polypeptide" as used herein interchangeably with the term "protein" describes linear molecular chains of amino acids, including single chain proteins or their fragments, containing more than 30 amino acids. The term "fragment of the protein" in accordance with the present invention refers to a portion of the protein comprising at least the amino acid residues necessary to maintain the biological activity of the protein. Polypeptides may further form oligomers consisting of at least two identical or different molecules. The corresponding higher order structures of such multimers are, correspondingly, termed homo- or heterodimers, homo- or hete rot rimers etc. Homo- or heterodimers etc. also fall under the definition of the term "polypeptide". Furthermore, peptidomimetics of such polypeptides where amino acid(s) and/or peptide bond(s) have been replaced by functional analogues are also encompassed by the invention. Such functional analogues include all known amino acids other than the 20 gene-encoded amino acids, such as selenocysteine. The term "polypeptide" also refers to naturally modified polypeptides where the modification is effected e.g. by glycosylation, acetylation, phosphorylation and similar modifications which are well known in the art.

In accordance with the present invention, the term "having cytochrome P450 monooxygenase activity" requires that the polypeptide encoded by the nucleic acid molecule of the invention has the biological activity of said enzyme. Cytochrome P450 monooxygenase activity preferably refers to the biological activity of enzymes of class E.C. 1 .14.-.-, more preferably of the P450 family CYP102. Such activity includes, without being limiting, at least one of monooxygenation of saturated and/or unsaturated fatty acids, alcohols, and/or amides; conversion of long chain alcohols and/or amines as well as conversion of lauric, myristic, and/or palmitic acids to omega-1 , omega-2, and/or omega-3 hydroxy analogues. Methods of determining said activity are well known to the person skilled in the art and include, for example, measuring the conversion of p-nitrophenoxydodecanoic acid (p-NCA) as described previously (Schwaneberg, U., Schmidt-Dannert, C, Schmitt, J., Schmid, R.D. 1999, A continuous spectrophotometric assay for P450 B -3, a fatty acid hydroxylating enzyme and its mutant F87A. Anal, Biochem 269: 359-366). Furthermore, the hydroxylation of BCC, BCC acid or DBCC as shown in the present invention (see examples) may also be used to assess cytochrome P450 monooxygenase activity.

The term "reductase domain", as used herein, refers to an amino acid sequence that functions as an electron donor. In particular, it serves as an electron donor for the oxygenase portion of a P450 enzyme, i.e. the heme domain. In cytochrome P450 BM3, represented by SEQ ID NO:2, the reductase domain starts at position 472 in SEQ ID NO:2 and ends at position 1048 in SEQ ID NO:2.

The term "mutation" in accordance with the present invention refers to changes in the amino acid sequence of a polypeptide and includes substitution, insertion, addition, inversion or deletion of one or more amino acids in the polypeptide. in accordance with the present invention, the polypeptide comprising a reductase domain that deviates by at least one mutation from the reductase domain of cytochrome P450 BM3, wherein the reductase domain of cytochrome P450 BM3 is represented by SEQ ID NO; 1 ; or (b) a reductase domain having at least 95% sequence identity to SEQ ID NO: 1 , is also referred to herein as the "mutant polypeptide" or the "variant polypeptide". The term "substitution" in accordance with the present invention, refers to (a) point mutation(s) resulting in an amino acid exchange as compared to the parent sequence.

A substitution is the preferred mutation, in accordance with this invention.

The term "insertion" in accordance with the present invention refers to the addition of one or more amino acids to the parent sequence, wherein the addition is not to the N- or C-terminal end of the polypeptide. The term "addition" in accordance with the present invention refers to the addition of one or more amino acids to the parent sequence, to the N- or C-terminal end of the polypeptide. In this case, the resulting mutant polypeptide may also be a fusion protein including for example amino acid sequence which confer desired properties such as modified/enhanced stability or solubility or tags for improved purification, such as for example a V5- or poly-His-tag or a tap- tag.

The term "deletion" as used in accordance with the present invention refers to the loss of one or more amino acids from the parent sequence; wherein the term does not include N-terminai or C-termina! truncations of the respective amino acid sequence.

The parent sequence, in accordance with the present invention, is a polypeptide comprising a reductase domain having either the sequence of SEQ ID NO:1 or at least 95% sequence identity to SEQ ID NO:1 . The parent sequence can for example be cytochrome P450 BM3 as represented by SEQ ID NO:2. which comprises an oxygenase (i.e. heme) domain and a reductase domain, wherein the reductase domain spans from amino acids 472 to 1048 of SEQ ID NO:2 and corresponds to SEQ ID NO: 1 (see Figure 4 for an alignment of SEQ ID NOs: 1 and 2). The coding sequence of cytochrome P450 BM3 is represented by SEQ ID NO:16. In a preferred embodiment, the mutant polypeptide of the invention is not a polypeptide resulting solely from a deletion of amino acids as compared to the parent sequence, in a more preferred embodiment, the mutant polypeptide of the invention deviates from the parent sequence in at least one amino acid substitution. In a further more preferred embodiment, the mutant polypeptide of the invention deviates from the parent sequence in that each of the at least one mutations in the reductase domain are amino acid substitutions. The term "deviates by at least one mutation" refers to any deviation by one or more mutations, such as for example at least two mutations, such as at least three mutations, such as at least four mutations, such as at least five mutations, such as at least six mutations, such as at least seven mutations, such as at least eight mutations, such as at least nine mutations, such as at least ten mutations, such as at least 12 mutations, such as at least 15 mutations, such as at least 20 mutations, such as at least 25 mutations, such as at least 30 mutations or at least 35 mutations. Preferably, the mutant polypeptides of the invention deviate from the parent sequence by less than 70 mutations, such as for example less than 50 mutations, such as less than 40 mutations. Any numerical values not explicitly mentioned above but falling within the above recited preferred ranges are also envisaged by the term "at least one mutation".

Methods for introducing mutations into the amino acid sequence of enzymes are well known in the art and include, without being limiting, directed evolution (e.g. Li, Q.S., Schwaneberg, U., Fischer, P., Schmid, R.D. 2000, Directed evolution of the fatty-acid hydroxylase P450 BM-3 into an indole-hydroxylating catalyst. Chemistry 6: 1531 -1536), saturation and sequence saturation mutagenesis (Miyazaki, K., Arnold, F.H. 1999, Exploring nonnatural evolutionary pathways by saturation mutagenesis: rapid improvement of protein function. J. Mol. Evol. 49: 716-720; Wong TS, Tee KL, Hauer B, Schwaneberg U 2004, Sequence saturation mutagenesis (SeSaM): a novel method for directed evolution, Nucleic Acids Res. 10, 32(3) e26.), random mutagenesis (e.g. Chen, K., Arnold, F.H. 1993, Tuning the activity of an enzyme for unusual environments: sequential ramdom mutagenesis of subtilisin E for catalysis in dimethylformamide. Proc. Natl. Acad. Sci. USA 90: 5618-5622; McCullum E.O., Williams B.A., Zhang J., Chaput J.C. 2010, Random mutagenesis by error-prone PGR, Methods Mol Biol. 634:103-9) and others. Directed evolution has been described previously as a suitable way to introduce mutations into enzymes to generated variants with novel enzymatic properties (e.g. Sachis et al. (2008), Improved PCR method for the creation of saturation mutagenesis libraries in directed evolution: application to difficult-to-amplify templates. Appl. Microbiol. Biotechnol. 81 (2): 387-97; Stemmer, W. (1994), Rapid evolution of a protein in vitro by DNA shuffling, Nature 370, 6488: 389-391 ; Tee KL, Schwaneberg U. (2007) Directed evolution of oxygenases: screening systems, success stories and challenges, Comb Chem High Throughput Screen 10: 197-217. Review). Also WO 2001/042455 describes this method to engineer biosynthetic pathways by directed evolution techniques, while directed evolution of oxygenase enzymes, amongst them P450 oxygenase, was further disclosed in WO 01/77368 A1.

Directed evolution offers many advantages over the rational design approach, especially in the cases where a crystal structure of the enzyme is not available. Microtiter plate and solid phase screening systems, with throughput of 10 ² -10 ⁶ , are commonly applied screening formats for improving enzyme properties when it comes to oxygenases. They are usually laborious, cost ineffective and even under optimal conditions allowing only small number of variants to be screened. This limits one to use libraries generated in low mutagenesis conditions i.e. 1 -2 amino acid changes per gene. Recently, new techniques with ultra high throughput (>10 ⁷ ), based on fluorescent detection and flow cytometry have been published (Miller, O.J. et al. (2006), Directed evolution by in vitro compartmentalization, Nat Methods 3(7), 561 -70). Ultra high throughput methods are either based on surface display technology or in vitro compartmentalization (IVC) within double emulsions. The latter approach enabled development of flow cytometry based screening systems which, compared to display techniques, can be extended to intracellular/excreted enzymes with a soluble reaction product. Most important is that IVC enables physical connection between the gene (encoding active variant of enzyme) and the reaction product (fluorescent probe). In case when gene library (DNA) is entrapped, enzyme variants are directly expressed within the droplet using cell-free expression system. This approach has been successfully applied for directed evolution of DNA polymerases, phosphotriesterases, methyltransferases, endonucleases and galactosidases. Mutant polypeptides of the invention can for example be obtained by codon exchange within SEQ ID NO: 3, which represents a nucleic acid molecule encoding the reductase domain of SEQ ID NO:1 . Thus, in accordance with the present invention, "a nucleic acid molecule encoding a polypeptide comprising a reductase domain that deviates by at least one mutation from the reductase domain of SEQ ID NO: 1 " preferably is a nucleic acid molecule comprising a sequence that deviates from the sequence of SEQ ID NO:3 by at least one nucleic acid mutation resulting in a mutation of the reductase domain represented by SEQ ID NO:1 as defined above.

The present invention further encompasses nucleic acid molecules which additionally comprise silent mutations, i.e. mutations that do not lead to an amino acid mutation. Further comprised are nucleic acid molecules which are additionally altered in accordance with the codon usage of a specific origin or host organism, as well as nucleic acid molecules comprising a sequence that further deviates from the nucleic acid molecule of SEQ ID NO:3 due to the degeneracy of the genetic code (i.e. without altering the corresponding amino acid sequence) or that encode a polypeptide with additional conservative nucleotide substitution (i.e. the corresponding amino acid is replaced by another amino acid with the same charge. size, polarity and/or solubility and which encode a polypeptide according to the invention with an "increased cytochrome P450 monooxygenase activity"), and the corresponding complementary sequences. In accordance with the present invention the polypeptide of the invention may also comprise a reductase domain that deviates in at least one mutation from a "reductase domain having at least 95% sequence identity to SEQ ID NO:1 ". More preferably, said reductase domain has at least 96%, even more preferably at least 97% sequence identity to the reductase domain of SEQ ID NO:1 . Even more preferably the reductase domain has at least 98% sequence identity to the reductase domain of SEQ ID NO:1 and most preferably at least 99% sequence identity to the reductase domain of SEQ ID NO: 1 .

In accordance with the present invention, the term "% sequence identity" describes the number of matches ("hits") of identical nucleotides/amino acids of two or more aligned nucleic acid or amino acid sequences as compared to the number of nucleotides or amino acid residues making up the overall length of the nucleic acid or amino acid sequences (or the overall compared part thereof). In other terms, using an alignment, for two or more sequences or sub-sequences the percentage of amino acid residues or nucleotides that are the same (e.g., 80% or 85% identity) may be determined, when the (sub)sequences are compared and aligned for maximum correspondence over a window of comparison, or over a designated region as measured using a sequence comparison algorithm as known in the art, or when manually aligned and visually inspected. This definition also applies to the complement of a test sequence. Preferred nucleic acid molecules/polypeptides in accordance with the invention are those where the described identity exists over a region that is at least about 15 to 25 amino acids or nucleotides in length, more preferably, over a region that is at least about 50 to 100 amino acids or nucleotides in length. More preferred nucleic acid molecules/polypeptides in accordance with the present invention are those having the described sequence identity over the entire length of the nucleic acid molecule or polypeptide. Those having skill in the art will know how to determine percent sequence identity between/among sequences using, for example, algorithms such as those based on the NCBI BLAST algorithm (Stephen F. Aitschul, Thomas L. Madden, Alejandro A. Schaffer, Jinghui Zhang, Zheng Zhang, Webb Miller, and David J. Lipman (1997), "Gapped BLAST and PSI-BLAST: a new generation of protein database search programs", Nucleic Acids Res. 25:3389-3402), CLUSTALW computer program (Thompson Nucl. Acids Res. 2 (1994), 4673-4680) or FASTA (Pearson and Lipman, Proc. Natl. Acad. ScL, 1988, 85; 2444), as known in the art. The NCBI BLAST algorithm is preferably employed in accordance with this invention. The BLASTN program for nucleic acid sequences uses as default a word length (W) of 1 1 , an expectation (E) of 10, M=5, N=4, and a comparison of both strands. For amino acid sequences, the BLASTP program uses as default a word length (W) of 3, and an expectation (E) of 10. The BLOSUM62 scoring matrix (Henikoff, Proc. Natl. Acad. ScL, 1989, 89: 10915) uses alignments (B) of 50, expectation (E) of 10, =5, N=4, and a comparison of both strands. Accordingly, all the nucleic acid molecules having the prescribed function and further having a sequence identity of at least 95% as determined with the NCBI BLAST program fall under the scope of the invention.

In accordance with the present invention, the at least one mutation in the reductase domain is a "functional mutation". Thus, the altered amino acid sequence results in an increased cytochrome P450 monooxygenase activity as compared to a polypeptide comprising a reductase domain represented by SEQ ID NO:1. Such an increased cytochrome P450 monooxygenase activity results in a higher and/or faster substrate turn-over rate and may be due to, for example, an altered reactivity pattern or an altered substrate profile.

"Increased cytochrome P450 monooxygenase activity" includes, for the purposes of the present invention, an improved reactivity such as an increase in specific activity (for example expressed as nmol reacted carboxylic acid/minute/nmol P450-enzyme) and/or an improvement in at least one kinetic parameter selected from amongst Kcat, Km and Kcat/Km. Preferably, the improvement is at least 1 .5-fold, such as, for example, at least 2-fold, at least 5-fold, at least 10-fold, at least 50-fold, at least 100-fold, at least 150-fold, at least 250-fold, at least 500-fold or at least 1000-fold, as compared to the parent sequence.

More preferably, where the mutant polypeptide of the invention comprises additional mutations, for example in the heme domain, previously known in the art to improve the enzymatic activity of polypeptides comprising the reductase domain represented by SEQ ID NO: 1 , then the mutant polypeptide of the invention preferably also possesses an improved reactivity (such as e.g. an increase In specific activity expressed for example as nmol reacted carboxylic acid/minute/nmol P450-enzyme and/or an improvement in at least one kinetic parameter selected from amongst Kcat, Km and Kcat Km) as compared to such previously mutated polypeptides, such as for example the cytochrome P450 BM3 as represented by SEQ ID NO:4. The above recited amounts of improvement apply inter alia.

Methods to investigate the kinetic properties of an enzyme are well known in the art and include, without being limiting, the determination of Michaelis-Menten parameters. The Michaelis-Menten equation, as shown below, is the basis for the majority of single-substrate enzyme kinetics:

V Rl

K M + [S]

The Michaelis constant K _M is defined as the substrate concentration at which the rate of the enzyme reaction is half of the maximum reaction rate V _max , i.e. V _max /2. There is typically one rate-determining enzymatic step that allows this reaction to be modelled as a single catalytic step with an apparent unimolecular rate constant k _cat . The apparent unimolecular rate constant k _cat is defined by the following reaction:

BS^B + P

The rate-limiting step in an enzymatic reaction is generally considered as one with a rate equal to K _cat . However, it has been found for the P450 enzyme that more than one step may have an influence on Kcat or K _ca ,/K _m . The efficiency of oxidation of a substrate by the monooxygenase is dependent on the electron transfer steps which are accomplished by the reductase domain of the P450 ho!oenzyme. The electron transfer from the substrate to P450 has been identified as a major rate-limiting step of the oxidation reaction (Guengerich, F.P. rate-limiting steps in Cytochrome P450 catalysis, Biol. Chem., 383, 1553-1564). Therefore, we set out to improve the enzymatic properties of the reductase domain in order to overcome the bottleneck in the catalytic cycle of P450.

In accordance with the present invention, novel P450 enzymes with hitherto not described mutations in the reductase domain of the enzyme were identified. These novel variants provide an improved cytochrome P450 monooxygenase activity as compared to the parent enzyme and are, therefore, particularly useful in chemical and biotechnological applications of P450 BM3, e.g. for organic synthesis, oxidation of fatty acids and industrial biotransformation of pharmaceuticals.

The role of the reductase domain as an electron donor for the monooxygenase domain is crucial for P450 enzyme activity and, consequently, for its biotechnological application. Electron transfer from the reductase to the hydroxylase domain was identified as one of the rate limiting steps within the P450 catalytic cycle (Guengerich, F.P. (2002) rate-limiting steps in cytochrome P450 catalysis, Biol. Chem._383: 1553-1564). Nevertheless, the potential of improving the electron transfer within the P450 system has so far been widely underestimated (Berhardt, R. (2006) Cytochromes P450 as versatile biocatalysts, J. Biotechnol. 124: 128- 145).

As shown in the examples below, modified P450 monooxygenases are provided that are based on BM3 parent enzymes that carry mutations in the heme domain of the enzyme that have previously been described in the literature. After mutagenesis of the sequence of P450 BM3 applying an error prone PGR method, recombinant clones were screened in enzyme assays with different substrates. Those enzymes with improved kinetic properties were sequenced in order to determine their respective primary structure on the nucleic acid level. The identified novel variants are characterized by the surprising fact that they carry mutations in the reductase domain of the holoenzyme and show altered enzymatic properties in that they exhibit significantly improved Michaelis-Menten parameters such as K _m and K _cat , expressed as enzymatic efficiency (K _cat /K _m ), as compared to the wild type and the parent mutant.

In a preferred embodiment, the mutant polypeptide having cytochrome P450 monooxygenase activity is derived from cytochrome P450 BM3, as represented by SEQ ID NO:2. In accordance with this embodiment, the mutant polypeptide of the invention deviates from the polypeptide of SEQ ID NO:2 by at least one mutation in the reductase domain of cytochrome P450 BM3, i.e. SEQ ID NO: 1 .

In a preferred embodiment of the nucleic acid molecule of the invention, at least one of said at least one mutations in the reductase domain occurs at a position in SEQ ID NO: 1 corresponding to position 812, 730, 648, 512, 857, 1030, 798, 883, 884 and/or 951 in SEQ ID NO:2.

The term "at least one of said at least one mutations in the reductase domain" as used herein refers to the fact that at least one of the mutations in the reductase domain has to occur at one of the recited positions. For example, if the mutant polypeptide of the invention comprises e.g. six mutations in the reductase domain, at least one of said six mutations has to occur at one of the recited positions. Thus, further mutations may occur in the reductase domain at positions other then the recited positions as long as at least one mutation occurs at one of the recited positions and provided that the preferred amount of overall mutations is as defined above with regard to the main embodiment. It is understood that a mutant polypeptide of the invention may also comprise, for example, mutations in two, three, four, five, six, seven, eight, nine or ten of the above recited positions.

The position of the respective mutations within SEQ ID NO:1 are provided by reference to the corresponding position in SEQ ID NO:2, which represents the full length cytochrome P450 BM3 polypeptide including the reductase domain represented by SEQ ID NO:1 . The sequence of SEQ ID NO: 1 corresponds to the sequence spanning from position 472 to position 1048 of SEQ ID NO:2, as shown in the sequence alignment provided in Figure 4. In other words, position 472 of SEQ ID NO:2 corresponds to position 1 of SEQ ID NO:1 . Furthermore, the preferred positions 812, 730, 648, 512, 857, 1030, 798, 883, 884 and/or 951 in SEQ ID NO:2 correspond to positions 341 , 259, 177, 41 , 386, 559, 327, 412, 413 and 481 , respectively, in SEQ ID NO:1 .

In a more preferred embodiment of the nucleic acid molecule of the invention, met at a position in SEQ ID NO:1 corresponding to position 812 in SEQ ID NO:2 is replaced by thr, ser, cys, asn, gin, asp or glu; ala at a position in SEQ ID NO: 1 corresponding to position 730 in SEQ ID NO:2 is replaced by val, gly, leu, ile, met, phe, trp or pro; asp at a position in SEQ ID NO: 1 corresponding to position 648 in SEQ ID NO:2 is replaced by gly, val, ala, leu, ile, met, phe, trp or pro; gin at a position in SEQ ID NO: 1 corresponding to position 512 in SEQ ID NO:2 is replaced by arg, lys or his; tyr at a position in SEQ ID NO:1 corresponding to position 857 in SEQ ID NO:2 is replaced by asn, gin, thr, ser, cys, asp or glu; leu at a position in SEQ ID ΝΟ.Ί corresponding to position 1030 in SEQ ID NO:2 is replaced by ser, tyr, asn, glu, tyr, thr, cys, asp or glu; leu at a position in SEQ ID NO:1 corresponding to position 798 in SEQ ID NO:2 is replaced by ser, tyr, asn, gin, tyr, thr, cys, asp or glu; thr at a position in SEQ ID NO: 1 corresponding to position 883 in SEQ ID NO:2 is replaced by his, lys, arg, phe, tyr or trp; pro at a position in SEQ ID NO: 1 corresponding to position 884 in SEQ ID NO:2 is replaced by arg, lys or his; and/or asn at a position in SEQ ID NO: 1 corresponding to position 951 in SEQ ID NO:2 is replaced by asp, glu, tyr, ser, cys, thr, asn or gin. The amino acids referred to herein are abbreviated in accordance with the established nomenclature employed in the art which is well known to the skilled person.

In an even more preferred embodiment, met at a position in SEQ ID NO: 1 corresponding to position 812 in SEQ ID NO:2 is replaced by thr; ala at a position in SEQ ID NO: 1 corresponding to position 730 in SEQ ID NO:2 is replaced by val; asp at a position in SEQ ID NO: 1 corresponding to position 648 in SEQ ID NO:2 is replaced by gly; gin at a position in SEQ ID NO:1 corresponding to position 512 in SEQ ID NO:2 is replaced by arg; tyr at a position in SEQ ID NO:1 corresponding to position 857 in SEQ ID NO:2 is replaced by asn; leu at a position in SEQ ID NO:1 corresponding to position 1030 in SEQ ID NO:2 is replaced by ser; leu at a position in SEQ ID NO: 1 corresponding to position 798 in SEQ ID NO:2 is replaced by ser; thr at a position in SEQ ID NO: 1 corresponding to position 883 in SEQ ID NO:2 is replaced by his; pro at a position in SEQ ID NO: 1 corresponding to position 884 in SEQ ID NO:2 is replaced by arg; and/or asn at a position in SEQ ID NO: 1 corresponding to position 951 in SEQ ID NO:2 is replaced by asp. In accordance with this preferred embodiment, a group of mutants is derived from Bacillus megaterium cytochrome P450 monooxygenase BM-3, which has the amino acid sequence as shown in SEQ ID NO: 2. These mutants deviate from the sequence of SEQ ID NO:2 as shown in table 1 below, wherein at least one of said mutations occurs in one of the following amino acid sequence positions: M812T, A730V, D648G, Q512R, Y857N, L1030S, L798S, T883H, P884R, N951 D.

In some embodiments, the mutations in question are shown in the one-letter amino acid code. The original amino acid is shown before the number which indicates the sequence position of the mutation, while the modified amino acid is shown after the number.

In another preferred embodiment of the nucleic acid molecule of the invention, the polypeptide having cytochrome P450 monooxygenase activity deviates by at least one further mutation from cytochrome P450 BM3, wherein cytochrome P450 BM3 is represented by SEQ ID NO:2. The term "at least one further mutation" as used herein relates to at least one mutation in addition to the above recited mutation(s) in the reductase domain, wherein the further mutation is in a part of the polypeptide other than the reductase domain, such as for example in the heme domain of the polypeptide. The definitions provided above with regard to mutations apply mutatis mutandis also to this/these further mutation(s). Thus, in accordance with the present invention, the resulting mutant polypeptide has an increased cytochrome P450 monooxygenase activity as compared to the polypeptide of SEQ ID NO:2. In a preferred embodiment, a mutant polypeptide of the invention deviating by at least one further mutation from the polypeptide of SEQ ID NO:2 possesses a more increased cytochrome P450 monooxygenase activity as compared to a mutant polypeptide only deviating by at least one mutation in the reductase domain of SEQ ID NO:1 or a reductase domain having at least 95% sequence identity to the reductase domain of SEQ ID NO: 1. In this regard, a "more increased cytochrome P450 monooxygenase activity" refers to an at least 1 .5-fold higher increases in cytochrome P450 monooxygenase activity, such as for example an at least 2-fold higher increase, such as an at least 3-fold higher increase, such as an at least 5-fold higher increase, such as an at least 10-fold higher increase, such as an at least 50-fold higher increase, such as an at least 100-fold higher increase, such as an at least 500-fold higher increase or such as an at least 1000-fold higher increase.

In a more preferred embodiment, at least one of said at least one further mutations occurs at a position corresponding to position 87, 471 , 47, 29, 189, 13, 162, 354, 429, 64 and/or 223 in SEQ ID NO:2.

Mutations at the above recited positions in the heme domain of P450 monooxygenase are well known in the art. For example, Arg47 is thought to interact with carboxyl groups of fatty acids, thus stabilizing the negative charge of the substrate through ionic interaction. Amongst others, these residues have an important role on substrate recognition and conversion (Noble, M.A., Miles, C.S., Chapman, S.K. , Lysek, D.A., MacKay. A.C., Reid, G.A., Hanzlik, R.P. and Munro, A.W. (1999) Roles of key active-site residues in flavocytochrome P450 BM3. Biochem J. 339: 371 -379). These previously described mutations in the heme domain of P450 BM3 may for example be comprised in the parent enzymes used as starting proteins for generating improved variants in accordance with the present invention.

In a particularly preferred embodiment of the nucleic acid molecule encoding a polypeptide having cytochrome P450 monooxygenase activity deviating by at least one further mutation from cytochrome P450 BM3, the further mutations are a mutation at a position corresponding to position 87 in SEQ ID NO:2 and a mutation at a position corresponding to position 471 in SEQ ID NO:2.

In a further more preferred embodiment of the nucleic acid molecule of the invention, phe at a position corresponding to position 87 in SEQ ID NO:2 is replaced by ala, g!y, val, leu, ile, met, trp or pro; arg at a position corresponding to position 471 in SEQ ID NO:2 is replaced by cys, ser, tyr, thr, asn, gin, asp or glu; arg at a position corresponding to position 47 in SEQ ID NO:2 is replaced by phe, tyr, leu, val, gly, ala, ile, met, trp or pro; leu at a position corresponding to position 29 in SEQ ID NO:2 is replaced by ser, thr, cys, asn, gin, asp or glu; gin at a position corresponding to position 189 in SEQ ID NO:2 is replaced by arg, lys or his; glu at a position corresponding to position 13 in SEQ ID NO:2 is replaced by gly, val, ala, leu, ile, met, phe, trp or pro; phe at a position corresponding to position 162 in SEQ ID NO:2 is replaced by leu, val, gly, ala, ile, met, phe, trp or pro; met at a position corresponding to position 354 in SEQ ID NO:2 is replaced by ser, asn, gin, tyr, thr, cys, asp or glu; tyr at a position corresponding to position 429 in SEQ ID NO:2 is replaced by cys, ser, asn, gin, tyr, thr, asp or glu; glu at a position corresponding to position 64 in SEQ ID NO:2 is replaced by gly, val, ala, leu, iie, met, phe, trp or pro; and/or arg at a position corresponding to position 223 in SEQ ID NO:2 is replaced by his, arg or lys.

In another more preferred embodiment of the nucleic acid molecule of the invention, phe at a position corresponding to position 87 in SEQ ID NO:2 is replaced by ala; arg at a position corresponding to position 471 in SEQ ID NO:2 is replaced by cys; arg at a position corresponding to position 47 in SEQ ID NQ:2 is replaced by phe, tyr or leu; leu at a position corresponding to position 29 in SEQ ID NO:2 is replaced by ser; gin at a position corresponding to position 189 in SEQ ID NO:2 is replaced by arg; glu at a position corresponding to position 13 in SEQ ID NO:2 is replaced by gly; phe at a position corresponding to position 162 in SEQ ID NO:2 is replaced by leu; met at a position corresponding to position 354 in SEQ ID NO:2 is replaced by ser; tyr at a position corresponding to position 429 in SEQ ID NO:2 is replaced by cys; glu at a position corresponding to position 64 in SEQ ID NO:2 is replaced by gly; and/or arg at a position corresponding to position 223 in SEQ ID NO:2 is replaced by his.

In a more preferred embodiment, the combination of further mutations present in the mutant polypeptide of the invention are selected from the group consisting of: (a) F87A and R471 C; (b) F87A, R471 C and R47F; (c) F87A, R471 C, R47Y and L29S; (d) F87A, R471 C, R47L and E13G; (e) F87A, R471 C, F162L and M354S; or (f) F87A, R471 C, E64G, R223H and M354S.

Dm2#4 F87A/M354S/R471C SEQ ID NO: 12

D7 F87A/F162L/M354S/Y429C/R471 C SEQ ID NO: 13

E5 F87A/F162L/M354S/R471 C/L798S SEQ ID NO: 14

E64G/F87A/R223H/M354S/R471 C/T883H/P884R/N9

M3 SEQ ID NO: 15

51 D

Tabfe 1 : List of mutants of P450 BM3 employed herein as we I as starting sequences

(highlighted in gray)

In a further more preferred embodiment of the nucleic acid molecule of the invention, the polypeptide deviates from the polypeptide of SEQ ID NO:2 by an amino acid substitution pattern selected from the group consisting of: (a) F87A, R471 C and/or M 812 T; (b) F87A, R471 C, R47F and/or A730V; (c) F87A, R471 C, R47F and/or D648G; (d) F87A, R471 C, R47F and/or Q512R; (e) F87A, R471 C, R47Y, L29S, Q189R and/or Y857N; (f) F87A, R471 C, R47L, E13G and/or L1030S; (g) F87A, R471 C, F162L, M354S and/or L798S; and (h) F87A, R471 C, E64G, R223H, M354S, T883H, P884R and/or N951 D.

The invention furthermore relates to expression constructs comprising a nucleic acid sequence encoding a mutant according to the invention under the genetic control of regulatory nucleic acid sequences.

Preferably, the constructs according to the invention encompass a promoter 5 -upstream and a terminator sequence 3'-downstream of the encoding sequence in question, and, if appropriate, other customary regulatory elements, in each case operatively linked with the encoding sequence. Operative linkage is to be understood as meaning the sequential arrangement of promoter, encoding sequence, terminator and, if appropriate, other regulatory elements in such a manner that each of the regulatory elements can fulfil its intended function on expression of the encoding sequence. Non-limiting examples of operatively linkable sequences are targeting sequences, or else translation enhancers, polyadenylation signals, selection markers, amplification signals, replication origins and the like.

In addition to the artificial regulatory sequences, the natural regulatory sequence can still be present upstream of the actual structural gene. If desired, this natural regulation may also be switched off by genetic alteration, and the expression of the genes may be enhanced or lowered. However, the gene construct may also be simpler in construction, i.e. no additional regulatory signals are inserted upstream of the structural gene and the natural promoter with its regulation is not removed. Instead, the natural regulatory sequence is mutated in such a way that regulation no longer takes place and the gene expression is increased or reduced. One or more copies of the nucleic acid sequences may be present in the gene construct. Non-limiting examples of promoters are: cos, tac, trp, tet, trp-tet, Ipp, lac, Ipp-lac, laclq, T7, T5, T3, gal, trc, ara, SP6, l-PR or l-PL promoter, all of which are advantageously employed in gram-negative bacteria; as well as the gram-positive promoters amy and SP02, the yeast promoters ADC1 , MFa, AC, P-60, CYC1 , GAPDH or the plant promoters CaMV/35S, SSU, OCS, Iib4, usp, STLS1 , B33, nos, or the ubiquitin or phaseolin promoter.

In principle, all natural promoters with their regulatory sequences can be used. In addition, synthetic promoters may also be used in an advantageous fashion.

The abovementioned regulatory sequences are intended to allow the directed expression of the nucleic acid sequences. Depending on the host organism, this may mean, for example, that the gene is expressed or over-expressed only after induction has taken placed, or that the gene is expressed and/or over-expressed immediately, i.e. without induction.

The regulatory sequences or factors can preferably have a positive effect on expression and in this manner increase or reduce the latter. Thus, an enhancement of the regulatory elements may advantageously take place at the transcriptional level by using strong transcription signals such as promoters and/or "enhancers". In addition, translation may also be enhanced by improving, for example, mRNA stability. An expression cassette can be generated by fusing a suitable promoter with a suitable monooxygenase nucleotide sequence and a terminator signal or polyadenylation signal. The coding sequences can e.g. be synthesized by standard methods, or isolated from natural sources. For generating the expression cassette, customary recombination and cloning techniques are used as described, for example, by T. Maniatis, E. F. Fritsch and J. Sambrook, Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y. (1989); by T. J. Silhavy, M. L. Berman and L. W. Enquist, Experiments with Gene Fusions, Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y. (1984) and by Ausubel, F. M. et al., Current Protocols in Molecular Biology, Greene Publishing Assoc. and Wiley Interscience (1987).

The present invention further relates to a vector comprising the nucleic acid molecule or the expression construct of the invention.

For expression in a suitable host organism, the recombinant nucleic acid construct or gene construct is advantageously inserted into a host-specific vector which allows optimal gene expression in said host. Vectors are well known to the skilled worker and can be found, for example, in "Cloning Vectors" (Pouwels P. H. et al., Ed., Elsevier, Amsterdam-N.Y. -Oxford, 1985). Vectors are to be understood as meaning not only plasmids, but all other vectors known to the skilled worker such as, for example, phages, viruses such as SV40, CMV, baculovirus and adenovirus, transposons, IS elements, phasmids, cosmids, and linear or circular DNA. These vectors can be replicated autonomously in the host organism or chromosomally.

Non-limiting examples of vectors include prokaryotic plasmid vectors, such as the pUC-series, pBluescript (Stratagene), the pET-series of expression vectors (Novagen) or pCRTOPO (Invitrogen) and vectors compatible with an expression in mammalian cells like pREP (Invitrogen), pcDNA3 (Invitrogen), pCEP4 (Invitrogen), pMCI neo (Stratagene), pXT1 (Stratagene), pSG5 (Stratagene), EBO-pSV2neo, pBPV-1 , pdBPVMMTneo, pRSVgpt, pRSVneo, pSV2-dhfr, plZD35, pLXIN, pSIR (Clontech), pIRES-EGFP (Clontech), pEAK-10 (Edge Biosystems) pTriEx-Hygro (Novagen) and pCINeo (Promega). Examples for plasmid vectors suitable for Pichia pastoris comprise e.g. the plasmids pA0815, pPIC9K and pPIC3.5K (all Invitrogen).

Furthermore, it is preferred that the vector of the invention comprises a selectable marker. Examples of selectable markers include neomycin, ampicillin, and hygromycin resistance and the like. Specifically-designed vectors allow the shuttling of DNA between different hosts, such as between bacteria and fungal cells or between bacteria and animal cells.

The vectors according to the invention allow the generation of recombinant microorganisms which can be transformed, for example, with at least one vector according to the invention and which can be employed for producing the mutants. The above-described recombinant constructs according to the invention can advantageously be introduced into a suitable host system and expressed. It is preferred to use usual cloning and transfection methods known to the skilled worker, for example co-precipitation, protoplast fusion, electroporation, retroviral transfection and the like, in order to bring about expression of the abovementioned nucleic acids in the expression system in question. Suitable systems are described, for example, in Current Protocols in Molecular Biology, F. Ausubel et a!., Ed., Wiley Interscience, New York 1997.

Thus, the present invention also relates to a host transformed with the vector of the invention, wherein the host is not a human and not a human embryo. Suitable host organisms are, in principle, all organisms which allow expression of the nucleic acids according to the invention, their allelic variants, and their functional equivalents or derivatives. Host organisms are to be understood as meaning, for example, bacteria, fungi, yeast, as well as plant or animal cells. Preferred organisms are bacteria such as those of the genera Escherichia such as, for example, Escherichia coli but also bacteria such as for example Streptomyces, Bacillus or Pseudomonas, eukaryotic microorganisms such as Saccharomyces cerevisiae, Aspergillus, and higher eukaryotic cells from animals or plants, for example Sf9 or CHO cells. In addition, expression of the gene product may also be brought about in transgenic organisms such as transgenic animals such as, in particular, mice, sheep, or transgenic plants. The transgenic organisms may also be knock-out animals or plants in which the corresponding endogenous gene has been eliminated, such as, for example, by mutation or partial or complete deletion. Such transgenic animals may be suitable as model organisms for example for testing potential pharmaceutical compositions in vivo.

Successfully transformed organisms may be selected by means of marker genes which are also contained in the vector or in the expression cassette. Examples of such marker genes are genes for resistance to antibiotics and genes for enzymes which catalyze a colour reaction causing the transformed ceil to be coloured. They may then be selected by means of automatic cell sorting. Microorganisms which have been transformed successfully with a vector and which carry a suitable gene for resistance to antibiotics (for example G418 or hygromycin) may be selected by suitable liquid or solid media containing antibiotics. Marker proteins presented on the cell surface may be exploited for selection by means of affinity chromatography.

The combination of the host organisms and the vectors which match the organisms, such as plasmids, viruses or phages, for example plasmids with the RNA polymerase/promoter system, the phages λ, μ or other temperate phages or transposons and/or further advantageous regulatory sequences, forms an expression system. The term "expression system" is to be understood as meaning, for example, the combination of mammalian cells, such as CHO cells, and vectors, such as pcDNA3neo vector, which are suitable for mammalian celis. As described above, the gene product may advantageously also be expressed in transgenic animals, for example mice, sheep, or transgenic plants. Equally, it is possible to program cell- free translation systems with the RNA derived from the nucleic acid.

Furthermore, the present invention also relates to a method of producing a polypeptide comprising culturing the host of the invention under suitable conditions and isolating the polypeptide produced.

Thus, for example a monooxygenase-producing microorganism is cultured, monooxygenase expression is induced, if appropriate, and the monooxygenase is isolated from the culture. In this manner, the monooxygenase according to the invention may also be produced on an industrial scale, if this is desired.

The microorganism can be cultured and fermented by known methods. Bacteria can, for example, be multiplied in TB or LB medium at a temperature of 20 to 40° C and a pH of 6 to 9. Suitable culture conditions are described in detail for example by T. Maniatis, E. F. Fritsch and J. Sambrook, Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y. (1989).

Unless the monooxygenase is secreted into the culture medium, the cells have to be disrupted, and the monooxygenase is then obtained from the lysate by known protein isolation methods. The cells may be disrupted as desired, for example by high-frequency ultrasound, by high pressure, such as, for example, in a French pressure cell, by osmolysis, by the action of detergents, lytic enzymes or organic solvents, by homogenizers, or by combining a plurality of the methods listed. The monooxygenase may be purified by known methods of chromatography, such as molecular sieve chromatography (gel filtration), such as chromatography on Q-Sepharose, ion-exchange chromatography and hydrophobic chromatography, and by other customary methods such as ultra-filtration, crystallization, salting out, dialysis and native gel electrophoresis. Suitable methods are described, for example, by Cooper, F. G., Bioche ische Arbeitsmethoden [Methods in Biochemistry], Verlag Walter de Gruyter, Berlin, New York or by Scopes, R., Protein Purification, Springer Verlag, New York, Heidelberg, Berlin.

To isolate the recombinant protein, it is especially advantageous to use vector systems or oligonucleotides which extend the cDNA by certain nucleotide sequences and thus encode altered polypeptides or fusion proteins for the purposes of simpler purification. Such modifications which are suitable are, for example, tags which act as anchors, for example the modification known as hexa-histidine anchor or epitopes which can be recognized as antigens of antibodies (described, for example, by Harlow, E. and Lane, D., 1988, Antibodies: A Laboratory Manual. Cold Spring Harbor (N.Y.) Press). These anchors can serve to attach the proteins to a solid support such as, for example, a polymer matrix, which may be filled into a chromatography column or used on a microtiter plate or on any other carrier, for example.

The present invention further relates to a polypeptide encoded by the nucleic acid molecule of the invention or produced by the method of the invention.

This polypeptide is also referred to herein as the mutant polypeptide of the invention or the variant polypeptide of the invention.

Further, the present invention relates to the use of the polypeptide of the invention in synthetic chemical transformation, biotransformation or fine chemical synthesis.

The term "synthetic chemical transformation" in accordance with the present invention reiates to chemical alteration of synthetic chemicals by the use of enzymes such as monooxygenases to obtain transformation products with altered properties, e.g increased biodegradability in the environment or desired chemical or biochemical activity.

The term "biotransformation" means alteration of compounds such as (but not limited to) nutrients, amino acids, toxins, or drugs either in the body or -by enzymatic biotransformation- in vitro. One major application is the production of chiral compounds as building blocks for more complex molecules such as pharmaceuticals or catalysts by oxidative reactions (e.g. redox enzymes) or asymmetric sythesis (e.g. dehydrogenases). Cytochromes are principal enzymes involved in oxidative metabolism of drugs and other xenobiotics. From the bioindustrial point of view these enzymes can be involved in diverse synthetic transformations such as hydroxylation of the alkanes and aromatic hydrocarbons, epoxidation of carbon- carbon double bonds and heteroatom oxygenation. Non-limiting examples Include the transformation of steroids and prostaglandins.

Fine chemicals are pure, single chemical substances that are commercially produced with chemical reactions into highly specialized applications. Fine chemicals produced can be categorized into active pharmaceutical ingredients and their intermediates, biocides, and specialty chemicals for technical applications. In chemical technology, a distinction is made between bulk chemicals, which are produced in massive quantities by standardized reactions, and fine chemicals, which are custom-produced in smaller quantities for special uses. For the synthesis of fine chemicals enzymes are required which catalyze chemical reactions with a high degree of specificity, especially entio- and stereoselectivity. Thus, the term "fine chemical synthesis", as used herein, refers to procedures for the regio- and stereo-controlled transformation of compounds involving oxidation or reduction reactions. This is accomplished by a wide range of catalysts, including organometallic systems, biocatalysts and biomimetics. Reactions in which the mutant polypeptides of the present invention may be employed include, without being limiting, hydroxylation reactions; oxidation of alcohols to aldehydes, ketones and carboxylic acids; reduction of ketones; and reduction of alkenes including α, β- unsaturated carbonyl compounds. Further non-limiting exemplary reactions include Baeyer- Vi!liger oxidations and epoxidation reactions. Furthermore, the enantioselective transformation of synthetic chemical or natural product-derived compound collections can be utilized for compound library synthesis, e.g. for screening purposes in drug discovery.

The present invention further relates to an oligo- or polynucleotide comprising or consisting of at least 10 contiguous nucleotides in length which specifically hybridize(s) to a portion of the nucleic acid molecule of the invention, wherein said portion comprises at least one of the mutations in the reductase domain in accordance with the present invention and preferably one of the mutations specifically mentioned herein above by reference to a nucleotide or amino acid position. In other terms, at least one nucleotide of the oligo-or polynucleotide pairs by hybridisation with a nucleotide of the nucleic acid molecule encoding the monooxygenase of the invention which constitutes a mutated nucleotide.

In the context of the present invention the term "oligo- or polynucleotide" refers to nucleic acid molecules of different length: an oligonucleotide is a nucleic acid molecule consisting of up to 30 bp, a polynucleotide is a nucleic acid molecule consisting of more than 30 bp. The oligo- or polynucleotides of the invention specifically hybridize(s) to the nucleic acid molecule of the invention. In other words, they only hybridise to the nucleic acid molecule of the invention but do not cross-hybridise to the parent enzymes, such as for example the nucleic acid molecule encoding the polypeptide of SEQ ID NO: 1 (i.e. SEQ ID NO:3) or the wild type P450 monooxygenase BM3 (SEQ ID NO: 16). In order to specifically hybridise, the oligo- or polynucleotides of the invention hybridise to at least one sequence comprising a mutation in accordance with the invention. The present invention also relates to a set of oligo- or polynucleotides of the invention, such as for example a set of at least two oligo- or polynucleotides, such as at least three oligo- or polynucleotides, such as at least four oligo- or polynucleotides, such as at least five oligo- or polynucleotides or such as at least 10 oligo- or polynucleotides of the invention.

The term "hybridises/hybridising" as used herein refers to a pairing of an oligo- or polynucleotide to a complementary strand of this oligo- or polynucleotide, which thereby form a hybrid.

It is well known in the art how to perform hybridisation experiments with nucleic acid molecules. Correspondingly, the person skilled in the art knows what hybridisation conditions she/he has to use to allow for a successful hybridization. The establishment of suitable hybridisation conditions is referred to in standard text books such as Sambrook, Russell "Molecular Cloning, A Laboratory Manual", Cold Spring Harbor Laboratory, N.Y. (2001 ); Ausubel, "Current Protocols in Molecular Biology", Green Publishing Associates and Wiley Interscience, N.Y. (1989), or Higgins and Hames (Eds.) "Nucleic acid hybridization, a practical approach" IRL Press Oxford, Washington DC, (1985).

"Stringent conditions" refers to hybridisation conditions under which the oligo- or polynucleotides that are capable of hybridizing to the polynucleotides of the invention or parts thereof do not cross hybridise to unrelated polynucleotides. Appropriate stringent hybridisation conditions for each nucleic acid sequence may be established by a person skilled in the art on well-known parameters such as temperature, composition of the nucleic acid molecules, salt conditions etc.; see, for example, Sambrook et al.. "Molecular Cloning, A Laboratory Manual": CSH Press, Cold Spring Harbor, 1989 or Higgins and Hames (eds.), loc. cit. , see in particular the chapter "Hybridization Strategy" by Britten & Davidson, 3 to 15. Such conditions comprise, e.g. an overnight incubation at 65°C in 4x SSC (600 mM NaCI, 60 mM sodium citrate) followed by washing at 65°C in 0.1x SSC for one hour. Alternatively, hybridisation conditions can comprise: an overnight incubation at 42°C in a solution comprising 50% formamide, 5x SSC (750 mM NaCI, 75 mM sodium citrate), 50 mM sodium phosphate (pH 7.6), 5x Denhardt's solution, 10% dextran sulphate, and 20 pg/ml denatured, sheared salmon sperm DNA, followed by washing in e.g. 0.1 -0.5x SSC at about 55-65X for about 5 to 20 min. Said conditions for hybridisation are also known by a person skilled in the art as "highly stringent conditions for hybridization". Changes in the stringency of hybridisation are primarily accomplished through the manipulation of formamide concentration (lower percentages of formamide result in lowered stringency), salt conditions, or temperature. It is of note that variations in the above conditions may be accomplished through the inclusion and/or substitution of alternate blocking reagents. Typical blocking reagents include Denhardt's reagent, BLOTTO, heparin, denatured salmon sperm DNA, and commercially available proprietary formulations. The inclusion of specific blocking reagents may require modification of the hybridisation conditions described above, due to problems with compatibility. Such modifications can generally be effected by the skilled person without further ado. The embodiment recited herein above preferably refers to highly stringent conditions.

A hybridization complex may be formed in solution (e.g., Cot or Rot analysis) or between one nucleic acid sequence present in solution and another nucleic acid sequence immobilized on a solid support (e.g., membranes, filters, chips, pins or glass slides to which, e.g., cells have been fixed). These oligo- or polynucleotides of the invention may, for example, be useful as probes in Northern or Southern Blot analysis of RNA or DNA preparations, respectively, or can be used as oligonucleotide primers in PCR analysis dependent on their respective size. Also comprised by the invention are hybridising oligo- or polynucleotides which are useful for analysing DNA-Protein interactions via, e.g., eiectrophoretic mobility shift analysis (EMSA). Preferably, said hybridising oligo- or polynucleotides comprise at least 10, such as at least 1 1 , such as at least 12, such as at least 13, such as at least 14, such as at least 15, such as at least 16, such as at least 17 nucleotides, but may also comprise at least 19, 25, 50, 100, 150, 200, 500 or more nucleotides, whereas oligonucleotides of a length lying between these values but not mentioned are explicitly encompassed as well. Preferably, the mutations of the present invention have a central location in said oligo- or polynucleotides. "Central" meaning most preferably that an equal number of nucleotides is located in the 5 - and 3' -direction adjacent to the position of the mutation. In a different preferred embodiment 60, 70, 80 or 90 percent of nucleotides are located in the 5'- or 3'-direction adjacent to the position of the mutation and the remaining nucleotides are located in the opposite direction.

The person skilled in the art is familiar with the preparation and the use of said probes (see, e.g., Sambrook and Russel "Molecular Cloning, A Laboratory Manual", Cold Spring Harbor Laboratory, N.Y. (2001 )). Said nucleic acid molecules may be chemically synthesized or transcribed by an appropriate vector containing a chimeric gene which allows for the transcription of said nucleic acid molecule in the cell.

The present invention further relates to a composition comprising the nucleic acid molecule of the invention, or the vector of the invention or the host of the invention or the polypeptide of the invention or the oligo- or polynucleotide of the invention.

The term "composition", as used in accordance with the present invention, relates to a composition which comprises at least one mutant polypeptide of the invention. It may, optionally, comprise furthermore excipients, additives and/or adjuvants. Examples of additional components include surfactants, such as for example anionic, non-ionic, amphoteric and/or cationic surfactants. The composition may optionally comprise further molecules capable of altering the characteristics of the mutant polypeptide of the invention thereby, for example, reducing, stabilizing, delaying, modulating and/or activating their function. Furthermore, the composition may comprise a plurality of different mutant polypeptides of the invention. The present invention further relates to a kit comprising the nucleic acid molecule, or the vector, or the host, or the polypeptide, or the oligo- or polynucleotide of the invention.

The various components of the kit may be packaged in one or more containers such as one or more vials. The containers or vials may, in addition to the components, comprise preservatives or buffers for storage.

Preferably, the nucleic acid molecule of the invention or the polypeptide of the invention or the oligo- or polynucleotides of the invention are in isolated form, i.e. they are an isolated nucleic acid molecule or an isolated polypeptide or isolated oligo- or polynucleotides. The term "isolated" as used herein refers to nucleic acid molecules, polypeptides or oligo- or polynucleotides removed from their original environment (e.g., the natural environment if it is naturally occurring, or a host cell if expressed exogenously), and thus is altered "by the hand of man" from its original environment. An isolated nucleic acid molecule, polypeptide or oligo- or polynucleotide generally is provided with fewer non-nucleic acid or non-proteinaceous components (e.g. lipids) than the amount of components present in a source sample.

Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. In case of conflict, the patent specification, including definitions, will prevail.

The present invention will be illustrated by the following experiment description and taking into consideration the appended figures. The broad scope of this invention is best understood with reference to the following examples, which are not intended to limit the inventions to the specific embodiments. The figures show:

Figure 1 : Schematic representation of the screening procedure and the enzyme reaction catalysed by P450 BM3

Figure 2: SDS-PAGE comparison of Cyt P450 BM3 purified by different ion-exchange methods (lanes 2 to 4). Lane 5 is a non purified sample (cell homogenate) while lane 1 represents molecular weight markers (Fermentas). Figure 3: Diagram of the improved enzymatic efficacies of the muteins expressed as Kcat/Km. A) with BCC as substrate, B) with BCC acid as substrate, and C) with DBCC as the substrate.

Figure 4: Sequence alignment of wild type P450 BM3 holoenzyme (SEQ ID NO: 2) and reductase domain (SEQ ID NO: 1 ); the reductase domain starts at position 472. Positions of mutations of the present invention within the reductase domain are indicated by bold characters and the preferred amino acid exchange is shown underneath the respective position. Examples

Example 1 : General methods and materials

1.1 Library preparation and library screening using flow cytometry in double emulsions. As a PCR template for P450 BM3 gene and library and library amplification pCWORI vector harbouring F87A/R471 C variant of BM3 was used (Prof. Frances Arnold, Caltech, Pasadena, USA). All libraries were constructed in pALXtreme-1 a vector (pET-28a(+) derivative where 63 % of the sequence have been deleted and lacl gene has been transferred to the genome of BL21 -Gold (DE3) under the control of Q1 promoter (Dr. Alexander Schenk, Jacobs University Bremen, Bremen, Germany). For plasmid isolation, constructs were transformed in E. coli XL10-Gold (Invitrogen, Karlsruhe, Germany) and for protein expression in BL21 -Gold (DE3) lac! ⁰¹ (Dr. Alexander Schenk). Cells were normally grown in LB _Kan media (50 pg/ml) unless stated otherwise. Substrates were synthesized as described below. The assay in the emulsion was assembled as described below. Concentrated Screening master mix was prepared by mixing 25 μΙ isocitric acid (80 mM), 25 μΙ NADPH (10 mM), 12.5 μΙ isocitrate dehydrogenase (0.5 U/μΙ) and 5 μΙ of fluorescein (500 μΜ). Cell suspension (40 μΙ) in buffer (0.1 M Tris-HCI pH 8.0) was mixed with concentrated Screening mix (13 μΙ), vortexed shortly and emulsified (see below).

The assay in the 96-well microtiter plate format ( TP) was performed using Corning (Hagen, Germany) 96-well black flat bottom plates. Cells expressing P450 BM3 variants were grown directly in the MTP, centrifuged and re-suspended in 100 μΙ of assay-mix (100 mM phosphate buffer pH 9.0, 54 μΜ PMB, 75 μΜ BCC Acid and 250 μΜ NADPH). Fluorescence was monitored using TECAN Safire (Crailsheim, Germany) MTP spectrofiuori meter (excitation: 400 nm, emission: 440 nm, gain: 55, z-position: 5000 μιτι, integration time: 40 ε and number of light flashes: 5). The P450 BM3 gene was amplified in error prone PGR (epPCR) conditions using balanced dNTPs, addition of Mn ²⁺ ions, decreasing the amount of template DNA and increasing the number of cycles (Cadwell, R.C. and Joyce, G.F. (1992) Randomization of genes by PGR mutagenesis. PCR Methods Appl, 2, 28-33). All PCRs were done in 50 μΙ volume using thin- wall PGR tubes (Sarstedt, Germany) and Eppendorf Gradient Cycler (Darmstadt, Germany). Reactions consisted of 1 X PCR buffer pH 9.2 (50 mM tris-HCI, 16 mM ammonium-sulphate, 1.75 mM magnesium-chloride and 0.1 % Tween 20), dNTPs (0.2 mM each), forward and reverse primer (400 nM each, forward primer: 5 ^! - A*C*C*A*T*G*G*G*C*A*G*C*ATGACAATTAAAGAAATGCCTCAGCCAAAAACG -3', reverse primer: 5 - G ^* G ^* C ^* T*T*T*G ^* T*T ^* A*G*C ^* TTACCCAGCCCACACGTCTTTTGCGTATC -3', (asterisks mark positions of phosphothioester bond), MnCI ₂ (0.2 mM), Tag polymerase (5 U) and template DNA (25 ng). Cycling was done as follows: 1 cycle of initial denaturation (94°C, 2 min), 35 cycles consisting of denaturation (94°C, 30 sec), annealing (67°C, 30 sec), elongation (72°C, 2 min) and 1 cycle of final elongation (72°C, 5 min). After PCR sample was purified using PCR purification kit (Qiagen, Hilden, Germany) and quantified via Nano Drop (ND-1000, Nano Drop Technologies, Delaware, USA). Gene was cloned in pALXtreme-l a vector using Phosphorothioate based Ligase Independent Gene cloning system (PlGe) and transformed in XL10-Gold cells. Several tubes of transformed cells were pooled and grown together in liquid LB _Kan media (4 ml, 37°C, 12 h, 250 rpm). Small aliquot (5 μί) of transformation mixture was plated on LB _Kan agar plates to determine transformation efficiency and size of primary library. Plasmid was recovered using Plasmid Prep Kit (Qiagen. Hilden, Germany) and re-transformed to expression strain BL21 -Gold (DE3) lac! ^Q1 . Induction of P450 BM3 variants was done by inoculating cells in LB _Kan media (4 ml) and growing them for 2 hours (37°C, 250 rpm). Then IPTG (0.5 mM) was added and expression was continued (30°C, 250 rpm) for an additional 3 hours. After this, cells were centrifuged (5900 x g, 3 min) and washed twice with ice cold PBS. Finally cells were re-suspended in activity buffer (0.1 mM tris pH 8.0) in concentration of 5 x 10 ⁶ cell/μΙ. Prior to emulsifi cation, celi suspension was passed trough a 5 pm filter. Cell suspension was mixed with concentrated screening master mix (25 μΙ isocitric acid (80 mM), 25 μΙ NADPH (10 mM), 12.5 μΙ isocitrate dehydrogenase (0.5 U/μΙ) and 5 μΙ of fluorescein (500 μΜ)).

Emulsifi cation was done as described previously (Miller, O.J., Bernath, K., Agresti, J.J., Amitai, G.. Kelly, B.T., Mastrobattista, E., Taly, V., Magdassi, S., Tawfik, D.S. and Griffiths, A.D. (2006) Directed evolution by in vitro compartmentalization. Nat Methods, 3, 561 -570) with decreasing the final volume of emulsion to 525 μΙ and using a Miccra D-1 (ART, Mullheim, Germany) homogeniser. After preparation of primary emulsion, substrate was added (1 μΙ of 200 mM BCC Acid in DMSO) and secondary emulsion was prepared immediately after. Emulsion was incubated on room temperature (2 h), in dark. For visualization of integrity of secondary emulsion fluorescent microscopy was used (Keyence BZ-8000, Neu-lsenburg, Germany, mercury lamp excitation, blue (450±20 nm) and green (520±20 nm) filters for emission).

For analysis and sorting, the emulsion was diluted 100 times in sterile PBS. Sample was run with speed 5 μΙ/min trough Partec CyFlow Space flow cytometer (Partec, Muenster, Germany). Sheet fluid (0.9% NaCI, 0.01 Triton X-100 in Milli-Q water) was filtered and autoclaved before use. Detection was "triggered" on green fluorescence (excitation: 488 nm, emission: 530 nm) coming from fluorescein used as an internal control dye. Analysis speed was approx. 6000-7000 events/sec while sorting speed was 5-10 events/sec. For sorting -0.1 - 0.01 % of active population was chosen and sorted in approx. 50 ml volume. The sorted sample was passed trough a 0.2 μηι filter, recovered In 1 ml of LB _Ka n media with shaking (1400 rpm, 10 min) and then inoculated in LB _Ka n media (4 ml). For the next round of enrichment, this was used as a pre-culture sample. Enrichment/sorting was repeated 3 times.

After each round, 100 μί of sorted sample was plated on LB _Kan agar plates with IPTG (5 μΜ) for activity assay and cell quantification. Ceils were grown overnight (37°C, 16 h). Activity assay was done by picking colony from the agar plate directly in 50 μΙ Assay mix (100 mM phosphate buffer pH 9.0, 54 μΜ PMB, 75 μΜ substrate (BCC, BCC acid or DBCC, respectively) and 250 μΜ NADPH)) in black flat bottom 386-well MTP. Fluorescence (excitation: 400 nm, emission: 440 nm) was monitored using TECAN Safire (Crailsheim, Germany) MTP spectrofluorimeter in 60 min periods (gain: 80, z-position: 8500 pm, integration time: 40 ps and number of light flashes: 10).

Finally, after the flow cytometry enrichment steps, ceils were grown on LB _an agar plates (37°C, 16 h) and picked into 150 μΙ LB _Kan media in flat bottom transparent 96-well MTP using sterile toothpicks. The suspension was grown (37°C, 900 rpm, 70% humidity, 16 h), diluted with glycerol (25% final) and stored on -80°C (Master plate). Replica of Master plate for activity testing was made in 150 μΙ LB _Kan media with supplements (0.5 mM δ-aminolevulinic acid, 0.5 mM thiamine, 1 x trace elements and 5 μΜ IPTG) in flat bottom black 96-well MTP and grown (30°C, 700 rpm, 70% humidity) for another 12 h. Plates were centrifuged (3200 x g, 10 min, 4°C) and the assay was done as described above. The most active clones (including the starting clone M0) were selected from MTP screening and inoculated in 4 ml LB _Kan media. Four milliliters of pre-culture was transferred to 250 ml TB _an media (in 1 I flask) with supplements (0.5 mM δ-aminolevulinic acid, 0.5 mM thiamine and 1 x trace elements), grown (37°C, 250 rpm) for 2 hours and then induced by addition of IPTG (0.5 mM). Protein was expressed (30°C, 250 rpm) for 8 hours. After expression, cell suspension was kept on ice. Expressed cells were centrifuged (3200 x g, 10 min, 4°C), re- suspended in 15 ml lysis buffer (0.01 M tris pH 7.8) and passed trough French press (3 times, 1500 bars). Cell lysate was cleared by centrifugation (21000 x g, 10 min, 4°C) and filtering (0.45 pm). Protein was purified using ion-exchange chromatography as follows: a sample (10 ml) was loaded on DEAE-ion exchange column equilibrated in 100 mM tris-HCI pH 7.8 (buffer A). The flow was kept constant (5 ml/min). Detection was absorbance set up for total proteins (280 nm) and for heme proteins (417 nm). The unbound sample was washed out with 2 CV of buffer A. A gradient of buffer B (100 mM tris-HCI pH 7.8 with 2 M NaCI) was adjusted to 5 % and loosely bound proteins were washed out (2 CV). Then a linear gradient of 5-20 % was set up in 5 CV. Cyt P450 BM3 was eluted in this region. After 20 % B gradient was adjusted to 100 % B in 2 CV and washing of the column (100 % B) was continued for another 2 CV. At the end, column was washed with buffer A, then with Milli-Q water and kept in 20 % ethanol. The peak corresponding to P450 BM3 was pooled (10 ml) and the concentration of protein was determined using CO binding method (Omura, T. and Sato, R. (1964) The Carbon Monoxide-Binding Pigment Of Liver Microsomes. I. Evidence For Its Hemoprotein Nature. J Biol Chem, 239, 2370-2378).The purity of the samples was confirmed by SDS-PAGE. Kinetic characterization was done in black flat bottom 96-well MTP in a final volume of 120 μΙ. Enzyme fractions were diluted 10-15 times in PBS and kept on ice. Assay was assembled as follows: 100 μΙ 0.1 M phosphate buffer pH 9.0, 10 μΙ enzyme solution and 2 μΙ of substrate. After incubation with shaking (750 rpm, 5 min), 8 μΙ of NADPH (10 mM) was added. Fluorescence (excitation: 400 nm, emission: 440 nm) was monitored for 10 minutes (1 min interval, gain: 80, z-position: 5500 μιτι, integration time: 40 ps and number of light flashes: 10). Slope (AU/min) was calculated in the first 5 minutes of the reaction (linear range) using Microsoft Excel. Concentration of the product was calculated form the standard curve constructed for 3-carboxy coumarin (10-325 nM). For determination of standard deviation, 5 repetitions were done for each substrate concentration. For K _m and k _cat determination, data was plotted and fitted using Origin 7.0 (OriginLab Corporation, Northampton, USA).

Sequencing of selected variants was done with MWG (Ebersberg, Germany), The sequence was analyzed using Vector NTI (Invitrogen, Karlsruhe, Germany).

1.2 Enzyme expression and purification

All variants are expressed using BL21 -Gold (DE3) lacl ^Q1 expression strain and pALXtreme vector. Pre-culture was inoculated from glycerol stock directly into 4 mL LB _Kan media and grown (37°C, 250 rpm) for 16 h. Aliquot of pre-culture (500 μΙ_) was transferred to 250 mL LB _Kan supplemented media (0.5 mM aminolevulinic acid, 0.5 mM thiamine, 1X trace elements and 5 μΜ IPTG). Variants were expressed (30°C, 250 rpm) for 14-16 hours.

After the expression phase, the cell suspension was centrifuged (3200 x g, 10 min, 4°C). The pellet was re-suspended in lysis buffer (15 mL of 10 mM tris-HCI pH 7.8) and lysed using French press (3 passes, 1500 bar). Cell homogenate was cleared out by filtration (21000 x g, 10 min, 4°C) and filtration (0.45 μπι Millipore filter).

P450 BM3 has previously been purified using DEAE ion-exchange chromatography with step elution of salt as described in Schwaneberg et. ai 1999, Fig.2 lane 2 and 3. For the purification of the mutants of the present invention we developed a slightly modified the protocol in a way that a gradient elution was used. Lane 4 in fig. 2 shows the result of this modification of this protocol using a gradient elution thep instead of a block gradient for elution. in detail, the filtered crude extract of recombinant E. coii was loaded on DEAE-ion exchange column equilibrated in 100 mM tris-HCI pH 7.8 (buffer A). The flow was kept constant (5 ml/min). Detection was accomplished by measuring the absorbance set up for total proteins (280 nm) and for heme proteins (417 nm). Unbound samples were washed out with 2 column volumes (CV) of buffer A. A gradient of buffer B (100 m tris-HCI pH 7.8 with 2 M NaCI) was adjusted to 5 % and loosely bound proteins were washed out (2 CV). Then a linear gradient 5-20 % B was set up in 5 CV. Cyt P450 BM3 was eluted in this region, well separated from contaminating proteins. After 20 % B the gradient was adjusted to 100 % B in 2 CV and washing of the column (100 % B) was continued for another 2 CV. At the end, column was washed with buffer A, then with Milli-Q water and kept in 20 % ethanol.

Example 2: Selection of the Parent Mutants

The wild type sequence of Cyt P450 BM3 has been deposited in GenBank/EMBL databank with the accession number J04832 or AAA87602.1 , respectively..

The P450 BM-3 single mutant F87A was used as starting template. This mutation was disclosed elsewhere (e.g. EP 1 196603 B1 , EP 1 196545 B1 , EP 1 196605 B1. US 7531335) .

Other parent enzymes, designated Dm1 (R47F/F87A/R471 C) and Dm2#4 (F87A/M354S/R471 C), comprise additional mutation sites which were previously described (Wong, T.S., Arnold, F.H., and Schwaneberg, U., 2004, Laboratory evolution of cytochrome P450 BM-3 monooxygenase for organic cosolvents. Biotechnology and Bioengineering 85, 3: 351 -358) and show a significantly improved enzymatic efficiency as compared to the wild type. The position 354 was exchanged from Met to Ser and this mutation has already been shown to affect enzyme activity towards different substrates (Nazor, J., Dannenmann, S., Adjei, R.O., Fordjour, Y.B., Ghampson, IT., Blanusa, M., Roccatano, D. and Schwaneberg, U. (2008) Laboratory evolution of P450 BM3 for mediated electron transfer yielding an activity- improved and reductase-independent variant. Protein Eng Des Sel, 21 , 29-35).

As is shown in Tab. 1 to 3 and was disclosed previously, these mutations in the parent enzymes have a dramatic effect on the catalytic efficiency (Kcat/Km) with all three substrates used for the kinetic characterization. Example 3: Enzyme expression and purification

All variants were expressed using BL21 -Gold (DE3) lacl ^Q1 expression strain and pALXtreme vector. Pre-culture was inoculated from glycerol stock directly into 4 mL LB _Kan media and grown (37°C, 250 rpm) for 16 h. Aliquot of pre-culture (500 pL) was transferred to 250 mL LB Kan supplemented media (0.5 mM aminolevulinic acid, 0.5 mM thiamine, 1 X trace elements and 5 μΜ IPTG). Variants were expressed (30°C, 250 rpm) for 14-16 hours. After the expression phase, the cell suspension was centrifuged (3200 x g, 10 min, 4°C). Pellet was re-suspended in lysis buffer ( 15 mL of 10 mM tris-HCI pH 7.8) and lysed using French press (3 passes, 1500 bar). Cell homogenate was cleared out by filtration (21000 x g, 10 min, 4°C) and filtration (0.45 pm Millipore filter).

Cyt P450 BM3 has previously been purified using DEAE ion-exchange chromatography with step elution of salt. We slightly modified the protocol in a way that gradient elution was used. First, loosely bound proteins were washed out with 5 % buffer B in 2 CV. Cyt P450 BM3 is was eiuted in -10 ml of elution buffer, at linear gradient of buffer B (5-20 % B), well separated from other contaminating proteins.

Purity of the protein was estimated to 90-95 % using SDS-PAGE (Figure 32). The result was confirmed by comparing concentrations of total proteins (determined with BCA method) and concentration of Cyt P450 BM3 (determined with CO binding method). After chromatography the protein purity was sufficient for kinetic characterization. Sequencing of selected variants was done with MWG (Ebersberg, Germany). The sequence was analyzed using Vector NTI (Invitrogen, Karlsruhe, Germany).

Example 4: Determination of the kinetic parameters of the mutants and comparison with the respective parent and the wild-type enzyme

Kinetic characterization was done in black flat bottom 96-well MTP (Corning) in final volume of 120 μΙ. Enzyme fractions were diluted 5 times in PBS and kept on ice. Assay was assembled as follows: 100 μΙ 0.1 M phosphate buffer pH 9.0, 10 μΙ enzyme solution and 2 μΙ of substrate dilution (0.24-125 μΜ, 10 concentrations). After incubation with shaking (750 rpm, 5 min) 8 μΙ of NADPH (10 mM) was added. Fluorescence (excitation: 400 nm, emission: 440 nm) was monitored for 10 minutes (1 min interval, gain: 80. z-position: 5500 pm, integration time: 40 us and number of light flashes: 10). Slope (AU/min) was calculated in first 5 minutes of the reaction (linear range) using Microsoft Excel. Concentration of the product was calculated form the standard curve constructed for 3-carboxy coumarin (10-325 nM). For determination of standard deviation 3 repetitions were done for each substrate concentration. For K _m and k _cat determination data was plotted and fitted using Origin 7.0 (OriginLab Corporation, Northampton, USA).

4.1 Substrates for screening for monooxygenase activity

All substrates used for the kinetic characterization of the mutants comprise a coumarine "core" which is derivatized at position 7 and 3. After the conversion by P450 monooxygenase 3- carboxy coumarin, or its derivates, are released. This leads to an increase in specific fluorescence (excitation 370-400 nm, emission 440-460 nm).

The BCC substrate has a 7-hydroxy group derivatized with a benzyl group (bound with an ether bond). Hydroxylation at the ccC atom of the benzyl group leads to fluorophore release. The carboxy group in position 3 is esterified with a methyl group so this substrates has no charge, BCC acid has a very similar structure to the previously mentioned BCC except that it possesses a negative charge due to chemically de-esterified carboxy group in position 3. This substrate is of Interest since P450 BM3 rarely has activity towards drug-like molecules containing charge. DBCC has two benzyl groups bound in position 7 and 3 with an ether and an ester bond, respectively. This makes this substrate the bulkiest one within the three substrates used in the present invention.

4.1 .1 Substrate preparation

The substrate 7-benzoxy-3-carboxy coumarin was synthesized starting from 3-carboxy coumarin methyl ester. In detail, synthesis was as described in the following.

Synthesis and characterization of 12-(4-methyl umbelliferone)-dodecanoic acid and methyl ester

Step 1 - protection of carboxylic group of fatty acid by esterification. For this step, 1 .275 g (4.57 mmol) of 12-bromo-dodecanoic acid was dissolved in 20 ml dry methanol. Next, 100 μΙ of concentrated H ₂ S0 was added. The reaction was incubated at 75°C for 3 hours. The process was monitored by TLC using petrol ether: ethyl acetate (2: 1 ) as a developing solution. For visualization phosphomolybdic acid system was used,

After the reaction was completed, the sample was evaporated using a Rotavap at 40° C for 10-15 minutes. The pellet was dissolved in CH ₂ C! ₂ and extracted twice with 10 ml of saturated KHC0 ₃ , once with distilled water and once with brine. The organic phase was separated, dried with MgS0 ₄ , filtered and evaporated using Rotavap.

Step 2 - Conversion of 4-MU into sodium salt. For this step, 0.80 g (4.54 mmol) of 4-MU was dissolved in 15 ml dry methanol. 0.18 g (4.50 mmol) of NaOH was added. The reaction was mixed with magnetic stirrer until NaOH completely dissolved. At this point, solution changed color to bright yellow. Methanol was evaporated using Rotavap

Step 3 - Attaching of fluorescent probe (4-MU) to fatty acid. The previously prepared sodium salt of 4-MU was dissolved in 15 ml DMSO and dried shortly (10 min) on 120°C using an oil bath. Then methyl ester of 12-bromo-dodecanoic acid was added (dissolved in 15 ml DMSO). The mixture was stirred at 160°C for 3 hours. Progress was monitored by TLC.

After the reaction the mixture was poured into 200 ml of ice cold distilled water and a white precipitate formed immediately. After 10-15 minutes the mixture was centrifuged (4000 rpm, 5 min). The pellet was dissolved in CH ₂ CI ₂ , extracted twice with saturated NaHC0 ₃ and twice with distilled water. The organic layer was dried with MgS0 ₄ , filtered and evaporated using Rotavap.

Step 4: De-esterification of the substrate - release of carboxyl group. The pellet from the previous step was dissolved in 25 ml potassium-metoxide (prepared by dissolving 0.8 g (20.46 mmol) of KOH in 5 ml of water and then filling it up to 50 ml with methanol). The reaction was incubated for 1 hour at 80°C. The sample was cooled down to room temperature and poured in -100 ml ice cold water (pH adjusted to ~1 with HCI). The formed precipitate was filte

For characterization by NMR, approx. 10 mg of both samples, ester and acid, were dissolved in 1 ml of CDCI ₃ . ¹³ C and ¹ H NMR spectra were recorded using a 400 MHz NMR (JOEL ECX 400, Peabody, USA). For fluorescent spectra characterization a stock solution of substrate was prepared in DMSO (15 mM). Dilutions of stock solution were made in buffer and 3D fluorescent spectra were recorded using TECAN Safire (Switzerland). Conversion of 12-(4-MU)-dodecanoic acid and methyl ester

To test the possibility of conversion of novel coumarin/fatty acid compounds by Cyt P450 BM3 the soluble purified enzyme was used. Activity was tested with Cyt P450 BM3 wild-type (Wt) and selected variants (F87A, F87A/R47Y, F87A/R47Y/M354S and Y51 F).

The assay was assembled as follows: 230 μΙ of buffer (50 mM phosphate, 50 mM tris-HCI pH 8.0 0.25 KCI), 5 μΙ substrate (15 mM in DMSO) and 10 μΙ soluble enzyme. Reaction was incubated for 5 minutes at room temperature. Conversion was initiated by addition of 20 μΙ NADPH (5 mM). Fluorescence was monitored using TECAN Safire (ex. 310 and 380 nm, em. 390 and 440 nm, respectively) in black flat bottom 96-well MTPs (Greiner Bio-One). After reaction, 3 μΙ of each sample was analyzed by TLC (petrol ether: ethyl acetate = 1 : 1 ). Visualization was by UV light (254 and 366 nm).

Synthesis and characterization of 7-benzoxy-4-MU

First, 0.5 g (2.84 mmol) of 4-MU was dissolved in 20 ml DMSO with stirring. 600 μΙ (3.51 mmol) of benzyl bromide was added together with catalytic amount of NaOH and mixture was refluxed at 100°C for 2 hours. After the reaction mixture was poured into ice cold water (-200 ml) and left over night. Precipitate was separated by filtration and dried in vacuum. Dry pellet was re-dissolved in CH ₂ CI ₂ . Chromatography was done on silica gel column using petrol ether: ethyl acetate (1 :1 ) for eiution. Fractions with target compound are pooled, solvent evaporated on Rotavap and pellet dried in vacuum, overnight.

1 ^

For NMR characterization 5 mg of purified compound was dissolved in 1 ml CDCI3. C and NMR spectra were recorded using a 400 MHz NMR (JOEL ECX 400, Peabody. USA).

Conversion of 7-benzoxy-4-MU

To test the conversion of coumarin/benzyl compound (crude) with Cyt P450 BM3, reaction was assembled as follows: 100 μΙ buffer (50 mM phosphate, 50 mM tris-HC! pH 8.0, 0.25 mM KCI), 2.5 μΙ substrate (15 mM in DMSO) and 10 μΙ enzyme. After 5 minutes incubation on room temperature reaction was initiated with addition of 10 I NADPH (10 mM). Conversion was done 1 hour at room temperature. Reaction products were analyzed by TLC using petrol ether: ethyl acetate (1 : 1 ) as a developer. Visualization was done under UV light (366 nm). Activity was tested for both, Cyt P450 BM3 wild-type (Wt) and selected variants (F87A, F87A/R47Y, F87A R47Y/M354S and Y51 F).

For kinetic testing assay was assembled as described in the paragraph above. Fluorescence was monitored using TECAN Safire (ex. 380 nm, em. 440 nm, gain 50) in 60 minutes period (5 minutes interval).

To test applicability of NADPH-recycling system, assay was assembled as described in the paragraph above. Additionally, 5 μΙ of isocitric acid (80 mM) and 10 μ!_ of isocitrate dehydrogenase (0.01 U/pL) were added in reaction mix. The reaction was initiated with addition of 2.5 μΙ NADPH (5 mM). Fluorescence was monitored using TECAN Safire (ex. 380 nm, em. 440 nm, gain 50) in 60 minutes period (5 minutes interval).

The influence of the substrate concentration on the conversion reaction was tested in the following experiment. The reaction mix was assembled as follows: 100 μΙ buffer (50mM phosphate, 50mM tris-HCI pH 8.0, 0.25 KCI), 2.5μΙ substrate (different concentrations in DMSO), 10μΙ enzyme (Wt, 1 1 μΜ), 5μΙ isocitric acid (80mM), 10μΙ isocitric dehydrogenase (0.01 U/μΙ). The reaction mix was incubated 5 minutes at room temperature. The reaction was initiated by addition of 2.5μΙ of NADPH (5mM). Concentration of the substrate was ranging from 2.9mM to 23μΜ (in serial dilution by a factor of two). Fluorescence was monitored using TECAN Safire (ex. 380 nm, em. 440 nm, gain 50) in 160 minutes period (10 minutes interval). V ₀ was calculated for first 30 minutes of reaction (linear part). Synthesis and characterization of substrates for Cyt P450 BM3 using 3-carboxy coumarin (3-CC) as a fluorescent probe

Step 1 : Synthesis of methyl ester of 3-carboxy coumarine.

8.4 g (60.82 mmol) of 2,4-dihydroxybenzaldehyde was dissolved in 45 ml of anhydrous methanol. Solution was stirred and 8.7 g (65.85 mmol) of dimethyl malonate was added. Solution was brought to reflux temperature. 450 mg (5.16 mmol) of moprholine and 150 mg (2.49 mmol) of acetic acid were added to 2 ml of methanol and stirred until precipitate fully dissolved. This solution was then added to refluxed reaction mixture and reflux was continued for another 3 hours. After cooling, the product was filtered and re-crystallized from boiling methanol (-300 ml).

Step 2: Preparation of sodium salt of 3-CC.

For this step, 1.5 g (6.81 mmol) of 3-CC methyl ester was re-suspended in 50 ml of toluene, with stirring, and heated at 120°C until 5 ml of toluene evaporated (30-60 minutes). After cooling the mixture to room temperature 0.5 g (10.84 mmol) of NaH was added. Mixture was heated at 120°C and stirred until toluene evaporated (1 -2 hours). The obtained salt was dried in vacuum overnight.

Step 3: Attaching benzyl group to 3-CC methyl ester.

3 g (12.39 mmol) of prepared 3-CC methyl ester sodium salt was dissolved in 200 ml of DMF (dried with molecular sieves). Mixture was heated to 120°C. During heating, 2.138 g (12.5 mmol) of benzyl bromide was added. Mixture was kept on 120°C for 2 hours with stirring. Then, an additional 1 g (5.85 mmol) of benzyl bromide was added and reaction continued at 120°C for 4-6 hours. At the end, one more batch (0.7 g, 4.09 mmol) of benzyl bromide was added. Reaction was continued for an additional hour. At the end, mixture was cooled to room temperature for a few hours and poured to 400 ml of ice cold water. After precipitate formed (30-60 min), the suspension was filtered and rinsed with water. The precipitate was dried and re-dissolved in CH ₂ CI ₂ . Organic phase was extracted twice with water, filtered and evaporated on Rotavap. The precipitate was dried overnight in vacuum.

Target compounds were isolated after chromatography on silica gel. Sample was loaded in CH ₂ CI ₂ . Elution was done by adding small amount of ethyl acetate into CH ₂ CI ₂ (1 :20). Two main fractions were pooled according to TLC. Re-chromatography of un-pure Fraction II was done on silica gel using CH ₂ CI ₂ : ethyl acetate (20:1 ) for elution. Purity was monitored on TLC using the same solvent system.

Step 4: De-esterification of methyl ester group.

50 mg (161 .13 mol) of 7-benzoxy-3-carboxy coumarin methyl ester was dissolved in 4 ml THF (kept at 4°C). At the same time, 0.07 g (1 .67 mmol) of LiOH was dissolved in 4 ml of distilled water (kept at 4°C). When both components were cooled to 4°C they were mixed, stirred 1 hour on ice and left overnight in the fridge (with constant stirring). The following day, 1 .66 ml of 3M HCI was added to reaction mix and left to warm up to room temperature. Finally, 3.22 ml of brine was added and organic phases separated. Reaction mix was extracted three times with 20 ml ethyl acetate. All organic phases are pooled, evaporated on Rotavap and precipitate was dried overnight under vacuum. Purity was monitored by TLC.

For characterization by NMR, approx. 5 mg of both samples (Fraction 12 and Fraction 24) were dissolved in 1 ml of CDCI ₃ . ¹³ C and ¹ H NMR spectra were recorded using a 400 MHz NMR (JOEL ECX 400, Peabody, USA). Conversion of 3-carboxy coumarine based compounds using Cyt P450 BM3

Conversion of substrates based on 3-carboxy coumarine was done with purified Cyt P450 BM3. Tested variants included Wt and mutants F87A, F87A/R47F, F87A/R47Y, F87A R47F/M354S and Y51 F. The assay was assembled in black flat bottom 384-well MTPs (Greiner Bio-One) as follows: 50 μΙ buffer (100 mM phosphate buffer pH 9.0), 1 μΙ substrate (15 mM BCC and BCC Acid in DMSO, 10 mM DBCC in DMSO) and 5 μΙ enzyme (10 mg/ml). Reaction mix was incubated 5 minutes on room temperature. Reaction was initiated by addition of 4 μΙ NADPH (10 mM). Fluorescence was monitored in 1 min intervals for 40 minutes using TECAN Satire (TECAN Group, gain 70, z-position 7800). After the reaction 3 μΙ of each reaction mix was loaded and analyzed on TLC. Visualization was done by UV light (366 nm). Reverse phase HPLC was performed to analyze reaction products of conversion of BCC and BCC Acid by the Cyt P450 BM3 F87A R47F/M354S variant.

HPLC was performed on AKTA Purifier (GE Healthcare) connected to SOURCE 5RPC ST 4.6/450 column (GE Healthcare). Buffer A was 10 mM phosphate buffer pH 2.8 and buffer B was 90 % acetonitrile in 10 mM phosphate buffer pH 2.8. Flow was kept constant at 1 ml/min and detection was on 210 nm and 350 nm (specific for the coumarin structures). Sample (100 μΙ) was loaded in buffer A. Next, unbound sample was washed out with 2 CV of buffer A and linear gradient of buffer B (0-100 % in 10 CV) was applied. All target compounds were eluied in this region. Column was washed with 3 CV of buffer B (100 %). Four samples were prepared for each substrate and they included:

Sample 1 (100 μΙ) - blank: buffer + DMSO + NADPH + enzyme

Sample 2 (100 μΙ) - standard substrate: buffer + substrate

Sample 3 (100 μΙ) - standard product: buffer + 3-carboxy coumarin

Sample 4 (100 μΙ) - reaction mix: buffer + substrate in DMSO + NADPH + enzyme The reaction mix was incubated 2 hours at room temperature before analysis. Fractions containing unknown reaction products were collected and analyzed by TLC and by 3D spectral fluorimetry. 3D spectra were recorded using TECAN Safire (TECAN Group) and black flat bottom 96-well MTP (Greiner Bio-One).

For optimization of different excitation/emission wavelengths an assay was set up as follows: 50 μΙ buffer (100 mM phosphate buffer pH 7.5), 1 μΙ substrate (dilution in DMSO) and 5 μΙ enzyme (Cyt P450 BM3 139-3). Reaction mix was incubated on room temperature for 5 minutes. The reaction was initiated by addition of 4 μΙ NADPH (10 mM). The assay was done in black flat bottom 384-well MTPs (Greiner Bio-One). Fluorescence was monitored using TECAN Safire on three excitation (375, 400 and 405 nm) and three emission (455, 440 and 455 nm) wavelengths, respectively. Substrate concentrations were 167, 83, 42, 21 , 10 and 5.2 μΜ, respectively.

To test the effect of different permeabilizers (organic solvents and polymixin B sulphate - PMB) on conversion of BCC an experiment was set up as follows. E. coli DH5a harboring pCWORI vector with Cyt P450 BM3 Wt gene was expressed in TB _Amp media overnight (50 ml, 0.5 mM IPTG, 37°C, 250 rpm). After expression cells were centrifuged (4000 rpm, 10 min, 4°C) and washed twice with PBS. At the end, the cell pellet was re-suspended in 10 mi of activity buffer (100 mM phosphate buffer pH 7.5) and kept on ice. This concentrated cell suspension was used in assays. Assay was carried out as described in the paragraph above using only 167 μΜ substrate and adding 5 μΙ of cell suspension instead of purified enzyme. Organic solvents (ethanol, acetone, isopropanol and toluene) were added directly to the reaction mix in a final concentration of 10 % (vol/vol). Fluorescence (ex.400 nm, em. 440 nm) was recorded for 60 minutes (1 min interval).

After testing different permeabilizers the effect of different concentrations of PMB on activity was tested. DH5a expressing Cyt P450 BM3 Wt has been used. Assay was assembled as described in the paragraph above. Different amounts (1 -5 μΙ in 1 μΙ steps) of PMB stock solution (3.6 mM) have been added. Final volume of the reaction mix was kept constant by decreasing the volume of activity buffer. To test the difference in permeabi!ization potential between PMB and PMBN an experiment was set up as follows. DH5a cells expressing Cyt P450 BM3 139-3 variant have been used. The assay was assembled as described previously. Five and one μΙ of each permeabilizer stock (3.6 mM PMB or PMBN) was added in the reaction mix. Fluorescence was monitored for 60 minutes (1 min interval).

Dilutions of the substrates were made in DMSO and kept at 4°C (in the dark). Alternatively, the activity of P450 monooxygenases can be measured using substrates known in the art such as for example p-nitrophenoxydodecanoic acid (12-pNCA) as described in Schwaneberg, U., Schmidt-Dannert, C, Schmitt, J., Schmid, R.D., 1999, A continuous spectrophotometric assay for P450 BM-3, a fatty acid hydroxylating enzyme and its mutant F87A, Anal. Biochem. 269: 359-366).

All three substrates used herein are based on the same reporter molecule but all three have different properties (charge, bulky side groups etc). This was utilized for the directed evolution method for the discovery of new residues in Cyt P450 B 3 structure connected with specific activity and offers new options to improve its activity towards drug like molecules, charged molecules, bulky molecules etc..

Table 2: Structure and names of novel coumarine based substrates for screening Cyt P450 BM3 activity in MTP and double emulsions

Results of kinetic characterization with 3 substrates

The results of the Michaelis Menten assays with the wild type P450/BM3, the three parent muteins and the muteins of the invention applying the three different substrates are shown in Tables 3 to 5. The enzymatic activity is expressed by K _cat /K _M [eg/min μΜ]. The ratio of improvement of enzymatic efficacy as compared to the respective starting mutation is shown in the columns next to the column comprising the measured K _ca ,/K _M values.

Table 3: BCC as substrate

Table 4: BCC acid as substrate

Table 5: DBCC as substrate