Mutant mono-oxygenase cytochrome P450cam

The present invention relates to a mutant of the mono-oxygenase cytochrome P-450cam.
BACKGROUND OF THE INVENTION
Mono-oxygenases catalyse the selective oxidation of activated and unactivated carbon-hydrogen bonds using oxygen.sup.1, and are therefore of great interest for potential use in organic synthesis. However, progress in this area has been hampered by the difficulty in isolating sufficient quantities of the mono-oxygenase enzyme and/or the associated electron-transfer proteins. Despite the availability of amino acid sequences of more than 150 different cytochrome P-450 mono-oxygenases, to date structural date of only three are available.sup.2.3.4, and few have been successfully over-expressed in bacterial systems.sup.5.
One cytochrome P-450 mono-oxygenase, which is soluble and can be expressed in sufficient quantities, is the highly specific P-450cam from P. putida which catalyses the regio- and stereo-selective hydroxylation of camphor to 5-exo-hydroxycamphor.sup.6. The high resolution crystal structure of P-450cam has been determined.sup.2, and since the mechanism of action of this bacterial enzyme is believed to be very similar to that of its mammalian counterparts, it has been used as a framework on which structural models of mammalian enzymes are based.
The nucleotide sequence and corresponding amino acid sequence of P-450cam have been described.sup.5.7. The location of an active site of the enzyme is known and structure-function relationships have been investigated.sup.8.9. Mutants of P-450cam have been described at the 101 and 185 and 247 and 295 positions.sup.9.10.11. and at the 87 position.sup.12. A mutant in which tyrosine 96 (Y96) has been changed to phenylalanine 96 (the Y96F mutant) has been described.sup.11.13.14.15.. But in all cases the papers report effects of the mutations on the oxidation reactions of molecules which had previously been shown to be substrates for the wild-type enzyme. There is no teaching of how mutations might be used to provide biocatalysts for oxidation of different, novel substrates.
SUMMARY OF THE INVENTION
In an attempt to develop new biocatalysts, we have initiated a project which aims to redesign P-450cam, such that it is able more effectively to carry out specific oxidations of organic molecules whether or not these are substrates for the wild-type protein.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 illustrates that the three dimensional structure of P-450cam shows the active site to provide close van der Waals contact with the hydrophobic groups of camphor.
FIG. 2A and FIG. 2B are gas chromatographs in accord with the present invention.
The three dimensional structure of P-450cam shows the active site to provide close van der Waals contacts with the hydrophobic groups of camphor as shown in FIG. 1. Of particular significance are the contacts between camphor and the side chains of leucine 244, valine 247 and valine 295. Three aromatic residues (Y96, F87 and F98) are grouped together and line the substrate binding pocket, with a hydrogen bond between tyrosine 96 and the camphor carbonyl oxygen maintaining the substrate in the correct orientation to ensure the regio- and stereo-specificity of the reaction.
Lipscomb and co-workers.sup.16 demonstrated in 1978 that wild-type P-450cam showed a propensity to dimerise, but they also reported that the catalytic activity of the monomer and dimer towards camphor oxidation were indistinguishable. Since the dimerisation reaction could be reversed by thiol reducing agents, they concluded that it occurred by intermolecular cysteine disulphide (S--S) bond formation. They were unable to determine whether dimerisation involved more than one cysteine per P-450cam molecule. Nor were they able to identify the key cysteine residue(s) involved in this reaction because neither the amino acid sequence nor crystal structure of P-450cam were known at the time.
We used molecular modelling to investigate the likely effects of points mutations to the three aromatic residues (Y96, F87, F98) in the active site pocket. We noted that replacement of any of these aromatic residues with a smaller, hydrophobic non-aromatic side-chain could provide an "aromatic pocket" which could be used to bind more hydrophobic substrates. The program GRID.sup.17 was used to calculate an energy of interaction between an aromatic probe and possible mutants of cytochrome P-450cam where these residues were changed to alanine (F87A, Y96A and F98A). The results were then examined graphically using the molecular modelling package Quanta.sup.18.
The mutant F98A appeared to have the strongest binding interaction within the active site cavity accessible to the aromatic probe, with that of Y96A being slightly smaller, and that of F87A being substantially less. It was decided in the first instance to mutate tyrosine 96 to alanine as it is more central to the binding pocket, whereas phenylalanine 98 is in a groove to one side. Also, removal of tyrosine 96 should decrease the specificity of the enzyme towards camphor due to the loss of hydrogen bonding to the substrate.
According to one aspect of the present invention a mutant of the mono-oxygenase cytochrome p-450cam is provided in which the cysteine residue at position 334 is removed.
Preferably the removal is by the substitution of another amino acid except cysteine for the cysteine residue.
Alternatively the removal is by the deletion of the entire cysteine 344 residue from the enzyme.
Suitably the tyrosine residue at position 96 in the mutant is replaced by the residue of any amino acid except tyrosine.
Conveniently the amino acid is selected from any one of the following: alanine, arginine, asparagine, aspartic acid, cysteine, glutamic acid, glutamine, glycine, histidine, isoleucine, leucine, lysine, methionine, proline, serine, threonine, tryptophan, tyrosine and valine except that in the case of the cysteine residue at position 334, the amino acid is not cysteine and in the case of the tyrosine residue at position 96 the amino acid is not tyrosine.
Preferably the amino acid residue at one or more of the positions 87, 98, 101, 185, 193, 244, 247, 295, 297, 395 and 396 is replaced by another amino acid residue.
We examined the structure of P-450cam generated from the published crystallographic atomic co-ordinates using the modelling programme Quanta. We determined that there are five cysteines near the surface of P-450cam (cysteines 58, 85, 136, 148, 334) which might participate in intermolecular disulphide bond formation leading to protein dimerisation. We carried out sit-directed mutagenesis to substitute each of these cysteines to alanine, thus generating five Cys-Ala surface mutants.
The extent of protein dimerisation in the wild-type P-450cam and the five surface Cys-Ala mutants were investigated, The presence of dimer was detected by both anion exchange fast protein liquid chromatography on a Resource Q column (Pharmacia) and gel filtration size exclusion chromatography on a Superose 12 column (Pharmacia) in the wild-type P-450cam and the C58A, C85A, C136A and C148A mutants. On the other hand, no dimer was detected, even at high concentrations (0.1 mM range), for the C334A mutant (see data in FIG. 2). We concluded that wild-type P-450cam underwent dimerisation by intermolecular S--S disulphide bond formation between the surface cysteine 334 on two protein molecules.
The C334A mutation has the obvious benefit of removing unwanted protein dimerisation, thus ensuring the presence of a single species in solution at all times. In addition, we noted a completely unexpected benefit of this mutation. Like all proteins, wild-type P-450cam shows aggregation upon standing. The reasons why proteins aggregate are not clear, but the P-450cam aggregates are insoluble and catalytically inactive. The wild-type and C58A, C85A, C136A and C148A mutants all showed dimerisation as well as aggregation upon storage at 4.degree. C., and even in 50% glycerol solutions at -20.degree. C. Aggregation will also occur during turnover, especially at the higher P-450cam concentrations required in any economically viable industrial application in, for example, synthesis of organic molecules. The C334A mutant did not show any evidence of aggregation even at mM concentrations at room temperature over a period of three days. Thus, the C334A mutation has beneficial effects in protein handling, storage, and increased catalyst lifetime.
We believe the mutation at position 96 to be the key which enables the mutant enzymes to catalyse the oxidation of a relatively wide range of organic substrates. Other amino acids adjacent to the active site of the enzyme may also be mutated in order to change the shape and specificity of the active site. These other amino acids include those at positions 87, 98, 101, 185, 193, 244, 247, 295, 297, 395 and 396. It is envisaged that the amino acid at one or more of these positions may be replaced by: a small hydrophobic amino acid so as to enlarge the active site; or a large hydrophobic amino acid so as to reduce the size of the active site; or by an amino acid having an aromatic ring to interact with a corresponding aromatic ring of a substrate.
Regarding the oxidation reactions, the conditions are described in the literature references attached. The enzyme system typically includes putidaredoxin and putidaredoxin reductase together with NADH as co-factors in addition to the mutant enzyme. The example of cyclohexylbenzene oxidation is described in the experimental section below. Various classes of organic compounds are envisaged and described below. We note that the wild-type P-450cam is active towards the oxidation of a number of molecules included in the following sections. However, in all cases the mutant P-450cam proteins show much higher turnover activities.
i) The organic compound is an aromatic compound, either a hydrocarbon or a compound used under conditions in which it does not inactivate or denature the enzyme. Since the mutation has been effected with a view to creating an aromatic-binding pocket in the active site of the enzyme, the mutant enzyme is capable of catalysing the oxidation of a wide variety of aromatic compounds. Oxidation of example aromatic and polyaromatic compounds is demonstrated in the experimental section below and is believed very surprising given that the wild-type enzyme has been reported to catalyse the oxidation of only members of the camphor family and shows low activity towards a few other molecules such as styrene.sup.19, ethylbenzene.sup.9.10, a tetralone derivative.sup.20, and nicotine.sup.21.
ii) The organic compound may be a hydrocarbon, e.g. aliphatic or alicyclic, carrying a functional group (see Scheme 1). An aromatic protecting group is attached to the functional group prior to the oxidation reaction and removed from the functional group after the oxidation reaction. A suitable aromatic group is a benzyl group. The protecting group serves two purposes: firstly it makes the substrate more hydrophobic and hence increases binding to the hydrophobic enzyme pocket; secondly it may help to hold the substrate in place at the active site. Thus, with the correct aromatic protection group, both regio- and stereo-selective hydroxylation of the substrate may be achieved. Examples of monofunctionalised hydrocarbons are cyclohexyl, cyclopentyl and alkyl derivatives (Scheme 1). The oxidation products of these compounds are valuable starting materials for organic synthesis, particularly when produced in a homochiral form. A range of aromatic protecting groups are envisaged, e.g. benzyl or naphthyl ethers and benzoyl ethers and amides (Scheme 1). Of interest are also benzoxazole groups as carboxyl protecting groups and N-benzyl oxazolidine groups as aldehyde protecting groups. Both can be easily cleaved after the enzymatic oxidation and have previously been described in the literature for the microbial oxidations of aldehydes and acids.sup.22.
iii) The organic compound is a C4 to C12 aliphatic or alicyclic hydrocarbon. Oxidation of cyclohexane and linear and branched hydrocarbons is demonstrated in the experimental section below. We have found that wild-type P-450cam is also capable of oxidising these molecules, but the activities are low and in all cases the mutants show substantially higher activities.
iv) The organic compound is a halogenated aliphatic or alicyclic hydrocarbon. Oxidation of lindane (hexachlorocyclohexane) is also describe below.
Mutants were constructed in which active site substitutions were combined with the surface mutation of cysteine at position 334 to alanine and contained alanine, leucine, valine, or phenylalanine instead of tyrosine at position 96 (Y96). Lastly several active site mutations and the surface mutation were combined to constitute mutant enzymes with multiple mutations. The genes encoding cytochrome P-450cam, and its natural electron-transfer partners putidaredoxin and putidaredoxin reductase, were amplified from the total cellular DNA of P. Putida using the polymerise chain reaction (PCR). The expression vector/E. coli host combinations employed were pRH1091.sup.23 in strain JM109 for P-450cam, pUC 118 in strain JM109 for putidaredoxin, and pGL W11 in strain DH5 for putidaredoxin reductase. Oligonucleotide-directed site-specific mutagenesis was carried out using an M13 mp 19 subclone by the method of Zoller and Smith.sup.24, and mutant selection was by the method of Kunkel.sup.25.
Binding of potential substrates was investigated by spectroscopic methods. The wild-type enzyme in the absence of substrate is in the 6-co-ordinated, low-spin form with a weakly bound water occupying the sixth co-ordination site, and shows a characteristic Soret maximum at 418 nm. Binding of camphor and the substrate analogues adamantanone, adamantane and norbornane fully converted the haem to the 5-co-ordinated, high-spin form which has a characteristic Soret band at 392 nm. This haem spin-state shift is accompanied by an increase in the haem reduction potential which enables the physiological electron-transfer partner putidaredoxin to reduce P-450cam and initiate the catalytic hydroxylation cycle.sup.26. The haem spin state shift is thus a qualitative indication of the likelihood of molecules shown in Tables 1 and 2 being oxidised by the wild-type and mutant P-450cam enzymes.
A buffered solution (50 mM Tris.HCI, pH 7.4), typically 3 ml in volume, containing 10 uM putidaredoxin, 2 uM putidaredoxin reductase, 1 uM cytochrome P-450cam mono-oxygenase (wild-type or mutant), 200 mM KCI, 50 ug/ml bovine liver catalase (Sigma), and 1 mM target organic compound such as cyclohexylbenzene (added as a 0.1 M stock in ethanol) was preincubated at 30.degree. C. for 5 minutes. The enzymatic reaction was initiated by adding NADH to a total concentration of 2 mM. Further four aliquots of NADH (to increase the NADH concentration by 1 mM each time) were added in intervals of 10 minutes, and 30 minutes into the incubation one aliquot of substrate (to increase the concentration by 1 mM) was also added. The reaction was quenched after 60 minutes by adding 0.5 ml chloroform and vortexing the mixture. The phases were separated by centrifugation (4000 g) at 4.degree. C. The chloroform layer was analyzed by gas chromatography.
For many substrate compounds such as cyclohexylbenzene for which not all the P-450cam-mediated oxidation products are commercially available, the chloroform extracts are evaporated to dryness under a stream of nitrogen. The residues were extracted with hexane and the oxidation products separated by high performance liquid chromatography, eluting with a hexane/isopropanol gradient. The purified products were then identified by mass spectroscopy and particularly nuclear magnetic resonance spectroscopy.
For different substrates of different solubility in the aqueous buffer solution, the amount of substrate added to the incubation mixtures varies from 0.2 mM to 4 mM final concentration. The NADH concentration can be monitored at 340 nm and, in all cases, more substrates and NADH are added during the incubation.

Using the above experimental techniques, the inventors have investigated a considerable number of organic compounds as substrates for both the wild-type P-450cam enzyme and also the mutant version Y96A. Work has included mutants designated Y96V; Y96L; Y96f: C334A; the combined mutant F87A-Y96G-F193A and the combined active site and surface mutants of Y96A-C334A; Y96V-C334A; Y96L-C334A; Y96F-C334A; F87A-Y96G-F193A-C334A. The results for C334A and C334A-Y96A are set out in Table 1 and 2, in which structurally related molecules are grouped together.
Table 1 details the NADH consumption for oxidation of small linear, branched and cyclic hydrocarbons by the mutant Y96A-C334A. Tables 2(a) to 2(h) details the product distributions for mutant and substrate combinations where these have been elucidated to date.
The cysteine residue at position 344 can be deleted by any well known and freely available standard restriction techniques and will therefore not be described in detail herein.
______________________________________Scheme 1: Hydrocarbons #STR1## - #STR2## ---Z Protecting Group______________________________________ --OH #STR3## #STR4## - --NH.sub.2 #STR5## - --COOH #STR6## #STR7## - --CHO ##STR8##______________________________________
TABLE 1______________________________________ K.sub.app (.mu.M).sup.a WT Y96A______________________________________ 1 6.3 12 - 2 12 28 - 3 8.4 1.4 - 4 330 92 - 5 >1500.sup.b 73______________________________________ .sup.a Values are the average of two independent measurements using the method of Sligar (S. G. Sligar, Biochemistry, 1976, 15, 5399-5406). The value of K.sub.app is strongly dependent on the concentration of K.sup.+ in the buffer. At [K.sup.+ ] > 150 mM, K.sub.app for camphor is 0.6 .mu.M for both wildtype and Y96A. Data in this table were determined at [K.sup. ] = 70 mM in phosphate buffer, pH 7.4, in order to avoid # salting out o substrates at higher ion concentrations. .sup.b Saturation not reached.
TABLE 2(a)__________________________________________________________________________ Wild type Mutant Y96A Wild type Mutant Y96AP450cam-substrate interactions .DELTA.Spin .DELTA.Spin NADH NADH Subgroup: 1-ring high/low Vs DTT high/low Vs DTT turnover ? GC? turnover?__________________________________________________________________________ GC? Benzene -- -- -- -- - Toluene -- -- 30 30 - Ethylbenzene -- -- 40 - Styrene -- -- 30 30 - Cyclohexene -- 5 40 40 - 1,3-Cyclohexadiene nd nd nd nd - 1,4-Cyclohexadiene -- 5 15 20 - Cyclohexane -- -- 60 60 + - Hexane -- -- 70 60 + - Methylcyclohexane 50 50 100 70 - (S)-(+)-Carvone 10 60 10 80__________________________________________________________________________
TABLE 2(b)__________________________________________________________________________ Wild type Mutant Y96A Wild type Mutant Y96AP450cam-substrate interactions .DELTA.Spin .DELTA.Spin NADH NADH Subgroup: 2-ring, Naphthalene high/low Vs DTT high/low Vs DTT turnover ? GC? turnover?__________________________________________________________________________ GC? Naphthalene -- -- 15 20 - 1-Ethylnaphthalene -- -- 5 20 - 2-Ethylnaphthalene -- -- 10 20 - 2-Naphthylacetate -- 5 -- 5 - 1-Naphthylacetate -- 5 -- 5 - 1-Naphthylpropionate -- 20 0 20 - 1-Naphthylbutyrate -- 5 -- 5 - Naphthylphenylketone -- 5 -- 5 - 1,2-Dihydronaphthalene 5 20 30 90 - 1,2,3,4-Tetrahydro naphthalene 5 10 40__________________________________________________________________________ 40
TABLE 2(c)__________________________________________________________________________ Wild type Mutant Y96A Wild type Mutant Y96AP450cam-substrate interactions .DELTA.Spin .DELTA.Spin NADH NADH Subgroup: 2-ring, DPM high/low Vs DTT high/low Vs DTT turnover ? GC? turnover?__________________________________________________________________________ GC? Diphenylmeth ane -- 5 45 nd + + - Diphenylethe r 10 5 20 50 - Benzophenone -- 20 -- 20 - Cyclohexylph enylketone -- 30 60 nd - Phenylbenzoa te -- 5 -- -- - N-Phenylbenz ylamine 5 45 nd - Bibenzyl -- -- 55 55 - cis-Stilbene -- 20 40 50 - Biphenyl -- 20 -- 90 - Cyclohexylbe nzen 20 20 80 nd - trans-Stilbe ne -- -- -- -- - Benzylether -- 5 55__________________________________________________________________________ nd
TABLE 2(d)__________________________________________________________________________ Wild type Mutant Y96A Wild type Mutant Y96AP450cam-substrate interactions .DELTA.Spin .DELTA.Spin NADH NADH Subgroup: 3-ring high/low Vs DTT high/low Vs DTT turnover? GC? turnover? GC?__________________________________________________________________________ Anthracene - Phenanthrene -- -- 20 20 + - Fluorene -- -- -- 50 - 2-Fluorencar boxaldehyde -- -- -- 50 - 9-Fluorenone -- 20 -- 5 - Anthrone -- 5 -- 5 - Anthraquinon e - 2-Ethylanthr aquinone__________________________________________________________________________
TABLE 2(e)__________________________________________________________________________ Wild type Mutant Y96A Wild type Mutant Y96AP450cam-substrate interactions .DELTA.Spin .DELTA.Spin NADH NADH Subgroup: 4,5-ring high/low Vs DTT high/low Vs DTT turnover ? GC? turnover?__________________________________________________________________________ GC? Chrsene -- -- -- -- - 1,2-Benzanthracene -- -- -- -- - Fluoranthene -- 5 20 10 - Pyrene* -- -- -- -- - Perylene* -- -- -- --__________________________________________________________________________
TABLE 2(f)__________________________________________________________________________ Wild type Mutant Y96A Wild type Mutant Y96AP450cam-substrate interactions .DELTA.Spin .DELTA.Spin NADH NADH Subgroup: Cyclic Alkanes high/low Vs DTT high/low Vs DTT turnover ? GC? turnover?__________________________________________________________________________ GC? cis-Decahydr onaphthalene nd nd nd nd - trans-Decahy dro naphthale ne 20 10 90 70 - Cyclohexane -- -- 60 60 + - Methylcycloh exane 50 50 100 70__________________________________________________________________________
TABLE 2(g)__________________________________________________________________________ Wild type .DELTA.Spin Vs Mutant Y96A Wild type Mutant Y96AP450cam-substrate interactions high/ Vs .DELTA.Spin Vs NADH NADH Subgroup: n-Alkanes low DTT high/low DTT turnover? GC? turnover?__________________________________________________________________________ GC? n-Pentane -- 5 55 40 + n-Hexane -- -- 60 40 + n-Heptane 5 5 60 40 + n-Octane -- 5 80 45 + n-Nonane -- -- 70 45 + n-Decane nd nd nd nd n-Undecane nd nd 20 20 n-Dodecane nd nd 5 5 CH.sub.3 (CH.sub.2).sub.14 CH.sub.3 n-Hexadecane -- -- -- -- CH.sub.3 (CH.sub.2).sub.15 CH.sub.3 n-Heptadecane -- -- -- -- CH.sub.3 (CH.sub.2).sub.11 OSO.sub.3.Na SDS -- 20 -- 60 CH.sub.3 (CH.sub.2).sub.7 CH.dbd.CH(CH.sub.2).sub.7 CO.sub.2 H Oleic acid* -- 10? -- 20? [(CH.sub.3).s ub.2 CH(CH.sub .2).sub.3 CH(CH.sub.3)(C H.sub.2).sub.3 CH(CH.sub.3)C H.sub.2 CH.sub.2 --].sub.2 Squalane -- -- -- 20 - Isoprene -- -- 10__________________________________________________________________________ 10
TABLE 2(h)__________________________________________________________________________ Wild type Mutant Y96A Wild type Mutant Y96AP450cam-substrate interactions .DELTA.Spin .DELTA.Spin NADH NADH Subgroup: Camphor-like high/low Vs DTT high/low Vs DTT turnover ? GC? turnover?__________________________________________________________________________ GC? (1R)-(## -)-Camphorquinone 80 80 80 80 - (1R)-(-)-Fenchone 40 70 50 80 - Dicyclopentadiene 50 80 90__________________________________________________________________________ 90
TABLE 3______________________________________Turnover of Small Alkanes by P450cam Mutants All mutants listed below also contain the C334A mutation. Turnover rate measured as NADH consumption rate (nmole NADH/nmole P450cam/s). Alkane substrate:Main chain Wild length Name type Y96A______________________________________C4 n-butane -- -- C4 2-methyl butane background 4.6 C4 2,3-dimethyl butane background 16.8 C4 2,2-dimethyl butane background 14.0 C5 n-pentane background 5.8 C5 2-methyl pentane 3.8 11.7 C5 3-methyl pentane 1.3 14.2 C5 2,4-dimethyl pentane 0.2 12.6 C5 2,2-dimethyl pentane 5.2 12.8 C5 2,2,4-trimethyl pentane 0.9 5.3 C5 3-ethyl pentane background 16.2 C6 n-hexane background 6.0 C6 2-methyl hexane background 10.6 C7 n-heptane 2.7 4.4 C7 2-methyl heptane background 2.1 C7 4-methyl heptane 1.4 10.2 C8 n-octane background 5.8 C7 cycloheptane 4.4 42.5______________________________________ Product structures and distributions following oxidation of substrates with P450cam active site mutants. "background" - typical background NADH oxidation rate is 0.07 nmole NADH (nmole P450cam).sup.-1 sec.sup.-1 -
TABLE 4(a)__________________________________________________________________________Product structure and distributions following oxidation of substrateswith P450cam active site mutants. All mutants shown below also contain the C334Amutation.Cyclohexylbenzene Products (%) for mutants:Products WT Y96A Y96F Y96L Y96V__________________________________________________________________________ 3-ol 43 20 54 38 28L or D 3-ol 20 20 27 23 39 - ##STR69## Trans- 4-ol 25 15 6 23 10 - ##S Cis- 4-ol 12 45 13 16 23 -Total products(area/10.sup.5) 0.8 7.4 1.1 10.4 12.5 #STR71## - #STR72## - ##STR73##__________________________________________________________________________
TABLE 4(b)______________________________________ Products (%) for Phenylcyclohexene mutants:Products WT Y96A______________________________________ 3-one (A) 24 25 ##STR75## 3-ol (B) 76 75 -Total products(area/10.sup.6) 42 36 #STR76## - #STR77## - ##STR78##______________________________________
TABLE 4(c)__________________________________________________________________________ Products (%) for mutants:Naphthalene F87A-F96G- Products WT Y96A Y96F Y96L Y96V F193A__________________________________________________________________________ 1-ol 100 100 100 100 100 100 ##STR80## 2-ol 0 0 0 0 0 0 -Total products(area/10.sup.5) (0.016) 1.1 2.4 0.7 1.4 0.1 ##STR81##__________________________________________________________________________
TABLE 4(d)______________________________________ Products (%) for mutants:Phenanthrene F87A-F96G- Products WT Y96A Y96F Y96L Y96V F193A______________________________________A 38 49 41 35.5 41 27 B 15 23 31 41 38 41 C 12 13 5 9 11 3 D 35 15 23 14.5 10 29 Total products 0.075 7.0 4.5 2.8 1.6 0.065 (area/10.sup.6) ##STR82##______________________________________
TABLE 4(e)______________________________________ Products (%) for mutants:Fluoranthene F87A-F96G- Products WT Y96A Y96F Y96L Y96V F193A______________________________________A 0 84 -- -- -- 0 B 0 16 -- -- -- 100 Total products 0 2.7 -- -- -- 0.2 (area/10.sup.6) ##STR83##______________________________________
TABLE 4(f)______________________________________ Products (%) for mutants:Pyrene F87A-F96G- Products WT Y96A Y96F Y96L Y96V F193A______________________________________A 0 40 43 23 30 33 B 0 43.6 29 64.5 55 40 C 0 5 12.5 7.9 12 20 D 0 11.4 15.5 4.6 3 7 Total products 0 1.2 1.5 1.5 1.6 0.02 (area/10.sup.6) ##STR84##______________________________________
TABLE 4(g)______________________________________Lindane Products Products (%) for mutants(hexachlorocyclohexane) WT Y96A______________________________________A 100 100 Turnover rate 7.5 43.5 nmole NADH (nmoleP450).sup.-1 s.sup.-1 ##STR85##______________________________________
TABLE 4(h)______________________________________ Products(%) for mutants: Y96F Y96A______________________________________Hexane Products 2-hexanone 10 15 3-hexanone 16 28 2-hexanol 24 26 3-hexanol 50 32 Relative activity 18.2 25.5 (WT = 1) 2-Methyl hexane Products 2-methyl-2-hexanol 72 74 5-methyl-2-hexanone 16 14 2-methyl-3-hexanol 7 4 5-methyl-2-hexanol 5 8 Relative activity 2.3 2.6 (WT = 1)______________________________________
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__________________________________________________________________________# SEQUENCE LISTING - - - - <160> NUMBER OF SEQ ID NOS: 2 - - <210> SEQ ID NO 1 <211> LENGTH: 1242 <212> TYPE: DNA <213> ORGANISM: Pseudomonas putida <220> FEATURE: <221> NAME/KEY: P450cam WT <222> LOCATION: 1...1242 - - <400> SEQUENCE: 1 - - acg act gaa acc ata caa agc aac gcc aat ct - #t gcc cct ctg ccaccc 48 Thr Thr Glu Thr Ile Gln Ser Asn Ala Asn Le - #u Ala Pro Leu Pro Pro 1 5 - # 10 - # 15 - - cat gtg cca gag cac ctg gta ttc gac ttc ga - #c atg tac aat ccg tcg 96 His Val Pro Glu His Leu Val Phe Asp Phe As - #p Met Tyr Asn Pro Ser 20 - # 25 - # 30 - - aat ctg tct gcc ggc gtg cag gag gcc tgg gc - #a gtt ctg caa gaa tca 144 Asn Leu Ser Ala Gly Val Gln Glu Ala Trp Al - #a Val Leu Gln Glu Ser 35 - # 40 - # 45 - - aac gta ccg gat ctg gtg tgg act cgc tgc aa - #c ggc gga cac tgg atc 192 Asn Val Pro Asp Leu Val Trp Thr Arg Cys As - #n Gly Gly His Trp Ile 50 - # 55 - # 60 - - gcc act cgc ggc caa ctg atc cgt gag gcc ta - #t gaa gat tac cgc cac 240 Ala Thr Arg Gly Gln Leu Ile Arg Glu Ala Ty - #r Glu Asp Tyr Arg His 65 - #70 - #75 - #80 - - ttt tcc agc gag tgc ccg ttc atc cct cgt ga - #a gcc ggc gaa gcc tac 288 Phe Ser Ser Glu Cys Pro Phe Ile Pro Arg Gl - #u Ala Gly Glu Ala Tyr 85 - # 90 - # 95 - - gac ttc att ccc acc tcg atg gat ccg ccc ga - #g cag cgc cag ttt cgt 336 Asp Phe Ile Pro Thr Ser Met Asp Pro Pro Gl - #u Gln Arg Gln Phe Arg 100 - # 105 - # 110 - - gcg ctg gcc aac caa gtg gtt ggc atg ccg gt - #g gtg gat aag ctg gag 384 Ala Leu Ala Asn Gln Val Val Gly Met Pro Va - #l Val Asp Lys Leu Glu 115 - # 120 - # 125 - - aac cgg atc cag gag ctg gcc tgc tcg ctg at - #c gag agc ctg cgc ccg 432 Asn Arg Ile Gln Glu Leu Ala Cys Ser Leu Il - #e Glu Ser Leu Arg Pro 130 - # 135 - # 140 - - caa gga cag tgc aac ttc acc gag gac tac gc - #c gaa ccc ttc ccg ata 480 Gln Gly Gln Cys Asn Phe Thr Glu Asp Tyr Al - #a Glu Pro Phe Pro Ile 145 1 - #50 1 - #55 1 -#60 - - cgc atc ttc atg ctg ctc gca ggt cta ccg ga - #a gaa gat atc ccgcac 528 Arg Ile Phe Met Leu Leu Ala Gly Leu Pro Gl - #u Glu Asp Ile Pro His 165 - # 170 - # 175 - - ttg aaa tac cta acg gat cag atg acc cgt cc - #g gat ggc agc atg acc 576 Leu Lys Tyr Leu Thr Asp Gln Met Thr Arg Pr - #o Asp Gly Ser Met Thr 180 - # 185 - # 190 - - ttc gca gag gcc aag gag gcg ctc tac gac ta - #t ctg ata ccg atc atc 624 Phe Ala Glu Ala Lys Glu Ala Leu Tyr Asp Ty - #r Leu Ile Pro Ile Ile 195 - # 200 - # 205 - - gag caa cgc agg cag aag ccg gga acc gac gc - #t atc agc atc gtt gcc 672 Glu Gln Arg Arg Gln Lys Pro Gly Thr Asp Al - #a Ile Ser Ile Val Ala 210 - # 215 - # 220 - - aac ggc cag gtc aat ggg cga ccg atc acc ag - #t gac gaa gcc aag agg 720 Asn Gly Gln Val Asn Gly Arg Pro Ile Thr Se - #r Asp Glu Ala Lys Arg 225 2 - #30 2 - #35 2 -#40 - - atg tgt ggc ctg tta ctg gtc ggc ggc ctg ga - #t acg gtg gtc aatttc 768 Met Cys Gly Leu Leu Leu Val Gly Gly Leu As - #p Thr Val Val Asn Phe 245 - # 250 - # 255 - - ctc agc ttc agc atg gag ttc ctg gcc aaa ag - #c ccg gag cat cgc cag 816 Leu Ser Phe Ser Met Glu Phe Leu Ala Lys Se - #r Pro Glu His Arg Gln 260 - # 265 - # 270 - - gag ctg atc gag cgt ccc gag cgt att cca gc - #c gct tgc gag gaa cta 864 Glu Leu Ile Glu Arg Pro Glu Arg Ile Pro Al - #a Ala Cys Glu Glu Leu 275 - # 280 - # 285 - - ctc cgg cgc ttc tcg ctg gtt gcc gat ggc cg - #c atc ctc acc tcc gat 912 Leu Arg Arg Phe Ser Leu Val Ala Asp Gly Ar - #g Ile Leu Thr Ser Asp 290 - # 295 - # 300 - - tac gag ttt cat ggc gtg caa ctg aag aaa gg - #t gac cag atc ctg cta 960 Tyr Glu Phe His Gly Val Gln Leu Lys Lys Gl - #y Asp Gln Ile Leu Leu 305 3 - #10 3 - #15 3 -#20 - - ccg cag atg ctg tct ggc ctg gat gag cgc ga - #a aac gcc tgc ccgatg 1008 Pro Gln Met Leu Ser Gly Leu Asp Glu Arg Gl - #u Asn Ala Cys Pro Met 325 - # 330 - # 335 - - cac gtc gac ttc agt cgc caa aag gtt tca ca - #c acc acc ttt ggc cac 1056 His Val Asp Phe Ser Arg Glu Lys Val Ser Hi - #s Thr Thr Phe Gly His 340 - # 345 - # 350 - - ggc agc cat ctg tgc ctt ggc cag cac ctg gc - #c cgc cgg gaa atc atc 1104 Gly Ser His Leu Cys Leu Gly Gln His Leu Al - #a Arg Arg Glu Ile Ile 355 - # 360 - # 365 - - gtc acc ctc aag gaa tgg ctg acc agg att cc - #t gac ttc tcc att gcc 1152 Val Thr Leu Lys Glu Trp Leu Thr Arg Ile Pr - #o Asp Phe Ser Ile Ala 370 - # 375 - # 380 - - ccg ggt gcc cag att cag cac aag agc ggc at - #c gtc agc ggc gtg cag 1200 Pro Gly Ala Gln Ile Gln His Lys Ser Gly Il - #e Val Ser Gly Val Gln 385 3 - #90 3 - #95 4 -#00 - - gca ctc cct ctg gtc tgg gat ccg gcg act ac - #c aaa gcg gta - #1242 Ala Leu Pro Leu Val Trp Asp Pro Ala Thr Th - #r Lys Ala Val 405 - # 410 - # 414 - - - - <210> SEQ ID NO 2 <211> LENGTH: 1242 <212> TYPE: DNA <213> ORGANISM: Artificial Sequence <220> FEATURE: <221> NAME/KEY: P450cam C334A <222> LOCATION: 1 1242 <223> OTHER INFORMATION: Mutant with Cys-334 (tgc - #at nucleotides 1000 1002) substituted with Ala - - <400> SEQUENCE: 2 - - acg act gaa acc ata caa agc aac gcc aat ct - #t gcc cct ctg cca ccc 48 Thr Thr Glu Thr Ile Gln Ser Asn Ala Asn Le - #u Ala Pro Leu Pro Pro 1 5 - # 10 - # 15 - - cat gtg cca gag cac ctg gta ttc gac ttc ga - #c atg tac aat ccg tcg 96 His Val Pro Glu His Leu Val Phe Asp Phe As - #p Met Tyr Asn Pro Ser 20 - # 25 - # 30 - - aat ctg tct gcc ggc gtg cag gag gcc tgg gc - #a gtt ctg caa gaa tca 144 Asn Leu Ser Ala Gly Val Gln Glu Ala Trp Al - #a Val Leu Gln Glu Ser 35 - # 40 - # 45 - - aac gta ccg gat ctg gtg tgg act cgc tgc aa - #c ggc gga cac tgg atc 192 Asn Val Pro Asp Leu Val Trp Thr Arg Cys As - #n Gly Gly His Trp Ile 50 - # 55 - # 60 - - gcc act cgc ggc caa ctg atc cgt gag gcc ta - #t gaa gat tac cgc cac 240 Ala Thr Arg Gly Gln Leu Ile Arg Glu Ala Ty - #r Glu Asp Tyr Arg His 65 - #70 - #75 - #80 - - ttt tcc agc gag tgc ccg ttc atc cct cgt ga - #a gcc ggc gaa gcc tac 288 Phe Ser Ser Glu Cys Pro Phe Ile Pro Arg Gl - #u Ala Gly Glu Ala Tyr 85 - # 90 - # 95 - - gac ttc att ccc acc tcg atg gat ccg ccc ga - #g cag cgc cag ttt cgt 336 Asp Phe Ile Pro Thr Ser Met Asp Pro Pro Gl - #u Gln Arg Gln Phe Arg 100 - # 105 - # 110 - - gcg ctg gcc aac caa gtg gtt ggc atg ccg gt - #g gtg gat aag ctg gag 384 Ala Leu Ala Asn Gln Val Val Gly Met Pro Va - #l Val Asp Lys Leu Glu 115 - # 120 - # 125 - - aac cgg atc cag gag ctg gcc tgc tcg ctg at - #c gag agc ctg cgc ccg 432 Asn Arg Ile Gln Glu Leu Ala Cys Ser Leu Il - #e Glu Ser Leu Arg Pro 130 - # 135 - # 140 - - caa gga cag tgc aac ttc acc gag gac tac gc - #c gaa ccc ttc ccg ata 480 Gln Gly Gln Cys Asn Phe Thr Glu Asp Tyr Al - #a Glu Pro Phe Pro Ile 145 1 - #50 1 - #55 1 -#60 - - cgc atc ttc atg ctg ctc gca ggt cta ccg ga - #a gaa gat atc ccgcac 528 Arg Ile Phe Met Leu Leu Ala Gly Leu Pro Gl - #u Glu Asp Ile Pro His 165 - # 170 - # 175 - - ttg aaa tac cta acg gat cag atg acc cgt cc - #g gat ggc agc atg acc 576 Leu Lys Tyr Leu Thr Asp Gln Met Thr Arg Pr - #o Asp Gly Ser Met Thr 180 - # 185 - # 190 - - ttc gca gag gcc aag gag gcg ctc tac gac ta - #t ctg ata ccg atc atc 624 Phe Ala Glu Ala Lys Glu Ala Leu Tyr Asp Ty - #r Leu Ile Pro Ile Ile 195 - # 200 - # 205 - - gag caa cgc agg cag aag ccg gga acc gac gc - #t atc agc atc gtt gcc 672 Glu Gln Arg Arg Gln Lys Pro Gly Thr Asp Al - #a Ile Ser Ile Val Ala 210 - # 215 - # 220 - - aac ggc cag gtc aat ggg cga ccg atc acc ag - #t gac gaa gcc aag agg 720 Asn Gly Gln Val Asn Gly Arg Pro Ile Thr Se - #r Asp Glu Ala Lys Arg 225 2 - #30 2 - #35 2 -#40 - - atg tgt ggc ctg tta ctg gtc ggc ggc ctg ga - #t acg gtg gtc aatttc 768 Met Cys Gly Leu Leu Leu Val Gly Gly Leu As - #p Thr Val Val Asn Phe 245 - # 250 - # 255 - - ctc agc ttc agc atg gag ttc ctg gcc aaa ag - #c ccg gag cat cgc cag 816 Leu Ser Phe Ser Met Glu Phe Leu Ala Lys Se - #r Pro Glu His Arg Gln 260 - # 265 - # 270 - - gag ctg atc gag cgt ccc gag cgt att cca gc - #c gct tgc gag gaa cta 864 Glu Leu Ile Glu Arg Pro Glu Arg Ile Pro Al - #a Ala Cys Glu Glu Leu 275 - # 280 - # 285 - - ctc cgg cgc ttc tcg ctg gtt gcc gat ggc cg - #c atc ctc acc tcc gat 912 Leu Arg Arg Phe Ser Leu Val Ala Asp Gly Ar - #g Ile Leu Thr Ser Asp 290 - # 295 - # 300 - - tac gag ttt cat ggc gtg caa ctg aag aaa gg - #t gac cag atc ctg cta 960 Tyr Glu Phe His Gly Val Gln Leu Lys Lys Gl - #y Asp Gln Ile Leu Leu 305 3 - #10 3 - #15 3 -#20 - - ccg cag atg ctg tct ggc ctg gat gag cgc ga - #a aac gcc gcc ccgatg 1008 Pro Gln Met Leu Ser Gly Leu Asp Glu Arg Gl - #u Asn Ala Ala Pro Met 325 - # 330 - # 335 - - cac gtc gac ttc agt cgc caa aag gtt tca ca - #c acc acc ttt ggc cac 1056 His Val Asp Phe Ser Arg Glu Lys Val Ser Hi - #s Thr Thr Phe Gly His 340 - # 345 - # 350 - - ggc agc cat ctg tgc ctt ggc cag cac ctg gc - #c cgc cgg gaa atc atc 1104 Gly Ser His Leu Cys Leu Gly Gln His Leu Al - #a Arg Arg Glu Ile Ile 355 - # 360 - # 365 - - gtc acc ctc aag gaa tgg ctg acc agg att cc - #t gac ttc tcc att gcc 1152 Val Thr Leu Lys Glu Trp Leu Thr Arg Ile Pr - #o Asp Phe Ser Ile Ala 370 - # 375 - # 380 - - ccg ggt gcc cag att cag cac aag agc ggc at - #c gtc agc ggc gtg cag 1200 Pro Gly Ala Gln Ile Gln His Lys Ser Gly Il - #e Val Ser Gly Val Gln 385 3 - #90 3 - #95 4 -#00 - - gca ctc cct ctg gtc tgg gat ccg gcg act ac - #c aaa gcg gta - #1242 Ala Leu Pro Leu Val Trp Asp Pro Ala Thr Th - #r Lys Ala Val 405 - # 410 - # 414__________________________________________________________________________

Number	Date	Country	Kind
9522407	Nov 1995	GBX
PCT/GB9502588	Nov 1995	WOX

Number	Date	Country
2294692	May 1996	GBX
WO9516041	Jun 1995	WOX
WO 9534679	Dec 1995	WOX
WO 9614419	May 1996	WOX

Mutant mono-oxygenase cytochrome P450cam

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Entry
Smith, C. A. D., et al., 1992, "Debrisoquine hydroxylase gene polymorphism and susceptibilty to Parkinson's disease", The Lancet, vol. 339, pp. 1375-1377.
Tuck, S. F., et al., 1993, "Active sites of the cytochrome p450cam (CYP101) F87W and F87A mutants", The Journal of Biological Chemistry, vol. 268, pp. 269-275.
Dawson, E., et al., 1994, "An association study of debrisoquine hydroxylase (CYP2D6) polymorphisms in schizophrenia", Psychiatric Genetics, vol. 4, pp. 215-218.
J. Biological Chemistry, Dec. 15, 1988, vol. 263 No.35, pp. 18842-18849; William M. Atkins et al., "The Roles of Active Site Hydrogen Bonding in Cytochrome P450cam as Revealed by Site-directed Mutagenesis."
J. AM. Chem. Soc., 1989, vol 111, No. 7, pp. 2715-2717; William M. Atkins et al., "Molecular Recognition in Cytochrome P-450: Alteration of Regioselective Alkane Hydroxylation via Protein Engineering."
J. Biological Chemistry, Apr. 5, 1990, vol. 265, No. 10, pp. 5361-5363; Carmelo Di Primo et al., "Mutagenesis of a Single Hydrogen Bond in Cytochrome P-450 Alters Cation Binding and Heme Solvation."