Peptide amidase from xanthomonas

The invention is relative to a process for obtaining microorganisms containing peptide amidase, microorganisms obtained therewith, peptide amidases contained in them and the use thereof.
The invention is relative in particular to a screening process for microorganisms exhibiting peptide amidase activity in accordance with the generic part of claim 1; microorganisms obtained according to this process and deposited in conformity with claims 2-4; peptide amidases which can be isolated from the microorganisms according to claims 5-7 and the use thereof.
The following publications are cited regarding the state of the art:
(1) DE-OS 36 29 242,
(2) K. Breddam, Carlsberg Res. Commun. 49 (1984) 535-554,
(3) DE patent 40 14 564 and
(4) Y. Nishida et al., Enzyme Microb. Technol., 6 (1984), 85-90.
A peptide amidase is an enzyme which catalyzes the selective hydrolysis of a C-terminal amide function in a peptide amidase, that is, accelerates the following conversion: ##STR1##
Here, R' signifies a protective group for n=0 and for n>0 any amino acid, a protective group or H; n stands for zero or any whole number, R.sub.x are the side chains of the amino acids for n>0 whereas R.sub.1 signifies the side chain of the C-terminal amino acid.
The selective splitting off of the C-terminal amino group of peptide amides is generally difficult to achieve by a chemical conversion since the peptide bond is also subject to a hydrolytic attack. This results in mixtures which are difficult to separate and in low yields.
(1) teaches amidases for an enzymatic splitting off of the acid amide group which can only be used, however, on account of their .alpha.-amino acid amidase activity for the production of L-amino acids from .alpha.-unprotected D,L-amino acid amides. Peptide amides are not accepted.
(4) teaches the continuous production of N-Ac-L-Met from N-Ac-D,L-methionine amide in an enzymatic process using Erwinia carotovera.
Erwinia carotovera does contain an amidase activity; however, it is limited exclusively to amides of methionine. Thus, the enzyme from Erwinia carotovera only "splits off amino acid amide" and is not a peptide amidase. Furthermore, the enzyme from Erwinia carotovera can obviously only convert N-acetylated amino acid amides, in which conversion it is a disadvantage that the Ac protective group can only be split off with difficulty or not at all again.
On the other hand, peptidases are known which catalyze the hydrolytic splitting of the peptide bonds and of which it is only known that they have a certain secondary activity for splitting off the C-terminal amide protective group. An example for this is the carboxy peptidase Y, especially in chemically modified form (see (2)).
Thus, all these processes have serious disadvantages.
The state of the art according to (3) is also a peptide amidase which can be isolated from the flavedo of citrus fruits, especially of oranges. The peptide amidase described does not attack the peptide bond and catalyzes the splitting off of the free amino group from peptide amides. The peptide amidase known from (3) is characterized by the following parameters:
Splitting off of the C-terminal amino group from peptide amides and N-terminally protected amino acid amides;
No splitting of peptide bonds;
Optimum pH at 7.5.+-.1.5;
Good stability in the pH range between pH 6.0 and pH 9.0;
The optimum temperature is 30.degree. C. at a pH of 7.5;
Slight inhibition by inhibitors from serine proteases, especially phenylmethane sulfonyl fluoride;
The molecular weight is 23,000.+-.3,000;
Aggregate formation is occasionally observed;
The isoelectric point is approximately pH 9.5;
The enzyme does not accept any D-amino acid groups in C-terminal position and the rate of hydrolysis thereby is distinctly less than in the case of L-amino acid groups.
However, the isolated enzyme can be obtained from flavedo only in slight amounts and as a function of the season. More extensive studies also did not succeed, in spite of an approximately 500-fold enrichment, in preparing the protein in homogeneous form, so that molecular and genetic studies for improving the enzyme production were not able to be included due to lack of data.
However, this also renders the suggestion given in (3) moot that a microbial production of the enzyme can be achieved in a known manner by gene technology manipulation. The problems in the presentation of the homogeneous form do not allow manipulations of gene technology.
Therefore, in view of the problems associated with the state of the art the invention has the problem of making available a process for isolating microorganisms containing peptide amidase which makes possible a rapid selection of suitable strains. A further problem is also a stable peptide amidase which is more readily available than the known peptide amidase from flavedo at an equally high selectivity of the hydrolytic splitting off of the free amino group on the C-terminal end of peptide amides.
These problems and others not cited in detail are solved by a process with the features of the characterizing part of claim 1.
Microorganisms can be produced at practically any time of the year in any desired amount. Therefore, collection strains and isolated strains which can mobilize amide nitrogen as a source of nitrogen are analyzed for peptide amidase activity in a limited screening. Z-Gly-Tyr-NH.sub.2 was used as test substrate and the expected hydrolysis product Z-Gly-Tyr-OH determined by HPLC.
It is possible, by first incubating specimens containing microorganisms in a "double screening" in a nutrient medium containing amide nitrogen as nitrogen source and inoculating colonies subsequently produced onto a nutrient medium containing N-acetyl-D,L-methionine amide, incubating them and selecting the microorganisms which grow in both nutrient media, to find strains with an unusually good rate of success which are both relatively stable and also selective and active.
For the screening for microorganisms which can utilize amide nitrogen, samples of soil were suspended 4-6 hours in isotonic solution of common salt. The samples of soil were of any origin, including garden soil, forest soil, loamy or sandy soil. The solids were separated off at 2000 rpm by centrifugation. The supernatant was spread out onto agar plates and used to inoculate liquid media in Erlenmeyer flasks. The plates were incubated 3-7 days at 30.degree. C. and the Erlenmeyer flasks agitated at the same temperature at 120 rpm. Then, individual cultures were isolated from the plates and brought into pure culture by being multiply spread out. After this time aliquots were taken from the incubated Erlenmeyer flasks and fresh medium inoculated therewith. This process was repeated up to five times before specimens of the culture liquid were spread out after a suitable dilution onto plates. The nutrient medium for the solid and also for the liquid medium had the following composition:
______________________________________K.sub.2 HPO.sub.4 2.50 g/l KH.sub.2 PO.sub.4 1.95 g/l NaCl 1.00 g/l CaCl.sub.2 *2H.sub.2 O 0.05 g/l MgSO.sub.4 *7H.sub.2 O 0.3 g/l Yeast extract 0.50 g/l DL-carnitine amide 5.00 g/l Trace saline solution 0.80 ml/l Vitamin solution 2.5 ml/l (Agar for solid media 18.0 g/l) pH 7.2______________________________________
CaCl.sub.2 *2H.sub.2 O, MgSO.sub.4 *7H.sub.2 O as well as DL-carnitine amide and the vitamin solution (see below) were sterilized by filtration and added to the autoclaved, cooled-down medium. The trace saline solution was composed as follows:
______________________________________H.sub.3 BO.sub.3 75.0 mg MnCl.sub.2 *4H.sub.2 O 50.0 mg ZnCl.sub.2 187.0 mg CuSO.sub.4 *5H.sub.2 O 50.0 mg FeCl.sub.3 *6H.sub.2 O 625.0 mg (NH.sub.4).sub.8 Mo.sub.7 O.sub.24 *4H.sub.2 O 25.0 mg CoSO.sub.4 *7H.sub.2 O 37.5 mg H.sub.2 O demin. ad. 0.2 l.______________________________________
Individualized microorganisms grown on this medium were used for the screening for organisms with peptide amidase activity.
For the screening for microorganisms with peptide amidase activity a part of the organisms obtained above were spread out onto agar nutrient media and incubated 2 days at 30.degree. C. In order to obtain higher cell masses the cultures were enriched in 100 ml Erlenmeyer flasks with 20 ml medium. The incubation took place at 30.degree. C. for 2 days at 120 rpm. The nutrient medium used for this had the following composition:
______________________________________K.sub.2 HPO.sub.4 0.50 g/l KH.sub.2 PO.sub.4 2.00 g/l NaCl 1.00 g/l CaCl.sub.2 *2H.sub.2 O 0.05 g/l MgSO.sub.4 *7H.sub.2 O 0.10 g/l Glucose 5.00 g/l DL-carnitine amide 1.00 g/l N--Ac--DL--Met--NH.sub.2 2.00 g/l Yeast extract 0.50 g/l Vitamin solution 2.50 ml/l Trace saline solution 0.80 ml/l (Agar for solid media 18.00 g/l) pH 7.3.______________________________________
N-Ac-D,L-Met-NH.sub.2 was used as inductor thereby. Glucose should be avoided as a source of carbon so that the inductor is attacked from the N-terminus. Amides, glucose, CaCl.sub.2 *2H.sub.2 O, MgSO.sub.4 *7H.sub.2 O and the vitamin solution were sterilized by filtration and added to the autoclaved, cooled-down nutrient medium (see below for the composition of the trace saline solution and of the vitamin solution).
The cells were centrifuged, washed with 50 mM tris/HCl, pH 7.5 and taken up in this buffer (20-40% cell suspension). The cell maceration took place by wet grinding with glass beads 0.3 mm in diameter.
The raw extracts obtained therefrom were analyzed for the capacity to hydrolyze Z-Gly-Tyr-NH.sub.2.
Of 45 strains analyzed for deamidation 6 exhibited capacity to convert Z-Gly-Tyr-NH.sub.2 to Z-Gly-Tyr-OH. Table 1 shows selected data from the screening for peptide amidases.
TABLE 1______________________________________ Protein Strain content Spec. Activity No. OD.sub.660 * (mg BSAeq/ml) (mU/mg BSAeq)______________________________________ 4 0.98 1.93 4.84 11 1.22 5.30 9.70 18 1.13 5.96 2.97 21 0.87 7.90 5.22 22 1.04 9.40 7.23 42 1.58 3.46 2.82______________________________________ *OD.sub.660 = Optical density at a wavelength of 660 nm.
Isolated strains 4, 11, 18, 21, 22, 42 were deposited in the German Collection for Microorganisms DSM the name of the applicant.
______________________________________Strain No. DSM Deposit No. Deposition date______________________________________ 4 9182 5-2-1994 11 9181 5-2-1994 18 9183 5-2-1994 21 9184 5-2-1994 22 9185 5-2-1994 42 9186 5-2-1994______________________________________
Strain 11 was selected from the deposited pursuant to the Budapest Treaty strains for further analyses. Strain 11 was determined by the DSM (address: Mascheroder Weg 1b, D-38124 Braunschweig, Germany) as Stenotrophomonas maltophilia (Xanthomonas maltophilia). Strains 4, 18, 21, 22 and 42 were also evaluated, with the result that strains 4, 18, 21 and 22 likewise identified as Stenotrophomonas maltophilia (Xanthomonas maltophilia) and strain 42 as Ochrobactrum anthropi.
The invention also has as subject matter peptide amidases obtainable from the screened microorganisms.
The peptide amidase is formed intracellularly and can be isolated from the cells and purified according to processes familiar to the expert in the art.
The microbial peptide amidase is characterized by the following parameters:
Splitting off of the C-terminal amino group from peptide amides and N-terminally protected amino acid amides;
No splitting of peptide bonds;
Optimum pH at 6.0.+-.0.5;
Good stability in the pH range between pH 7 and pH 8;
The optimum temperature is 35-40.degree. C. at a pH of 7.5;
Inhibition of serine groups by inhibitors such as phenylmethane sulfonylfluoride as well as in particular 4-(2-aminoethylbenzylsulfonylfluoride) (Prefabloc);
The molecular weight is approximately 38,000 daltons (determined by gel filtration);
The isoelectric point is approximately pH 5.8.
The invention also comprises the isozymic forms of the microbial peptide amidase in accordance with the invention. The term "isozymic forms" in this connection denotes the enzymes in other microorganisms which catalyze the same reaction as the peptide amidase from Xanthomonas maltophilia.
Table 2 indicates some data for the purification of the peptide amidase from Xanthomonas maltophilia.
TABLE 2______________________________________ Spec. activity (mU/mg Purification Yield BSAeq) (-) (%)______________________________________Raw extract 4 1 100 Q-sepharose FF + 224 56 97 ultrafiltration Superdex G 75 + 1034 256 75 ultrafiltration IEF on the Mono 2133 533 63 P______________________________________
The purified peptide amidase from Xanthomonas maltophilia has in particular the following characteristic properties:
Purification of >500 at a yield of >60%
A molecular weight of 38000 da (gel filtration)
The isoelectric point is approximately pH 5.8
Temperature optimum between 37-45.degree. C.
pH optimum between 5-6.5
Temperature-stable at 20, 30 and 37.degree. C. over 3 days
At pH 7-8 the enzyme is stable at 30.degree. C. over 7 days
Upon the addition of 20% DMF the peptide amidase exhibits after 24 h a residual activity of 32% at a pH of 7.5
Serine group decisive for enzyme activity.
The N-terminal initial sequence of the peptide amidase from Xanthomonas maltophilia is (set forth in SEQ. ID No:1):
Xaa Arg Asn Val Pro Phe Pro Tyr Ala Glu Thr Asp Val 1 5 10 - Ala Asp Leu Gln 15 The first amino acid could not be determined. No comparable sequencecould be determined in the program Genepro 5.0 of the databank PIR,
The following table 3 compares the properties of the known, vegetable peptide amidase from flavedo of oranges (PAF) and of the microbial peptide amidase of the invention from Xanthomonas (PAX).
The peptide amidase of the invention shows in it neither peptidase activity nor amino acid amidase activity.
TABLE 3______________________________________ PAF PAX______________________________________Spec. activity (U/mg 100.1 2.13 BSAeq) Amino acid amidase 0 0 activity Peptidase activity 0 0 Molar mass (gel 23000 38000 filtration) pH optimum 6.5-8.7 5-6.5 Temperature optimum 30-35.degree. C. 37-45.degree. C. Isoelectric point 9.5 5.8 N-terminal sequence not known______________________________________
The microbial peptide amidases belonging to the invention are very advantageously suited for the catalysis of quite a number of reactions.
Thus, the microbial peptide amidases of the invention can be used with success to produce peptides and N-terminally protected amino acids of the general formula II ##STR2## in which R' is a protective group or any peptidically or isopeptidically bound amino acid- or peptide group and R.sub.1 signifies hydrogen or any side chain with enzymatic splitting off of a C-terminal amino group from a peptide amide or from an N-terminally protected amino acid amide.
In a preferred variant of the process this enzymatic reaction is carried out in a continuous manner.
It is also preferred that the deamidation is carried out as a process step of a coupled conversion with an enzyme system comprising proteases, peptidases, esterases and/or lipases. In this connection the selectivity of the peptide amidases of the invention is especially advantageous.
The microbial peptide amidases can also be used in accordance with the invention in processes for producing peptides of the above-mentioned type by the enzymatic conversion of optionally N-protected amino acid alkyl esters or optionally N-protected peptide alkyl esters with amino acid amides in aqueous phase or an aqueous-organic environment. The reaction takes place thereby in the presence of an enzyme which brings about the peptidic bonding and under enzymatic splitting off of the amide protective group; the synthesis is allowed to take place in a continuous manner, the peptide amide hydrolyzed by the peptide amidase enzymatically to the peptide and finally the peptide is separated on account of its charge from the reaction mixture and the amino acid amide returned.
Furthermore, the microbial peptide amidase of the invention can also be used for the splitting of racemic mixtures of N-protected amino acid amides in which a racemic mixture of N-protected amino acid amides is incubated with the peptide amidase and is reacted until the complete conversion of the N-protected L-amino acid amide and subsequently the N-protected L-amino acid is separated from the N-protected D-amino acid amide based on the differences of charge. Furthermore, according to the invention D-amino acids can also be produced. Thus, the N.sub..alpha. -protected L-amino acid amide can be selectively and enzymatically hydrolyzed e.g. within the scope of the invention by using the microbial peptide amidase of the invention, the N,-protected D-amino acid amide separated and converted by acid hydrolysis into the free D-amino acid. The amino acid amide racemates useful for the invention include, among others, N.sub..alpha. -formyl-DL-methionine amide, N.sub..alpha. -methylaminocarbonyl-DL-methionine amide, N.sub..alpha. -methoxycarbonyl-DL-methionine amide, N.sub..alpha. -ethoxycarbonly-DL-methionine amide, N.sub..alpha. -benzyloxycarbonyl-DL-methionine amide, N.sub..alpha. - acetyl-DL-neopentylglycine amide, N.sub..alpha. -benzyloxycarbonyl-DL-neopentylglycine amide.
Finally, the microbial peptide amidases of the invention can also be used with great advantage to obtain non-proteinogenous D-amino acids, preferably using sterically demanding, N-protected racemic amino acid amides such as N-acetyl-neopentylglycine amide, N-acetyl-naphthylalanine amide, naphthylalanine amide, N-acetylphenylglycine amide or similar derivatives. The N-acetyl-L-amino acid amides are enzymatically hydrolyzed, the N-acetyl-D-amino acid amides separated from the reaction mixture by chromatography and finally converted by acid hydrolysis into the free D-amino acids.
The N.sub..alpha. -protected D-amino acid amides obtainable by using the microbial peptide amidase of the invention from the preferred racemic, N.sub..alpha. -protected amino acid amides include e.g.: N.sub..alpha. -formyl-D-methionine amide, N.sub..alpha. -methylaminocarbonyl-D-methionine amide, N.sub..alpha. -methoxycarbonyl-D-methionine amide, N.sub..alpha. -ethoxycarbonyl-D-methionine amide, N.sub..alpha. -benzyloxycarbonyl-D-methionine amide, N-acetyl-D-neopentylglycine amide, N.sub..alpha. -benzyloxycarbonyl-D-neopentylglycine amide.

The invention is explained in the following in detail using examples. Further embodiments and particularities also result in particular from the attached figures, to which reference is made in the specification.
FIG. 1 shows the dependency of the conversion rate (%) on the pH for peptide amidase obtained from Xanthomonas maltophilia.
FIG. 2 shows a plotting of the relative activity against the time for peptide amidase from Xanthomonas maltophilia in various buffers at 30.degree. C.
FIG. 3 shows a plotting of the conversion rate as a function of the temperature for peptide amidase from Xanthomonas maltophilia.
FIG. 4 shows the temperature stability of the peptide amidase from Xanthomonas maltophilia.
FIG. 5 shows the kinetic determination of the conversion of Z-Gly-Tyr-NH.sub.2 with the peptide amidase from Xanthomonas maltophilia.
FIG. 6 shows the splitting of racemic mixtures of Z-D,L-Ala-NH.sub.2 with the peptide amidase from Xanthomonas maltophilia.
FIG. 7 shows the enantioselective deamidation of N-Ac-D,L-Met-NH.sub.2 with the peptide amidase from Xanthomonas maltophilia.
FIG. 8 shows the influence of solvent on the enzymatic activity of the peptide amidase from Xanthomonas maltophilia.
FIG. 9 shows the solvent stability of the peptide amidase from Xanthomonas maltophilia.

EXAMPLE 1
Production and workup of the peptide amidase from Xanthomonas maltophilia
1.1 Growth
40 g biomoist mass/l and an activity of 4 U/l were obtained in the partially optimized medium with the following composition. The media optimization took place with the aid of the genetic algorithm. The nutrient medium was autoclaved, glucose, N-Ac-DL-Met-NH.sub.2, CaCl.sub.2 *2H.sub.2 O, MgSO.sub.4 *7H.sub.2 O and the vitamin solution were added in a sterile manner.
______________________________________N--Ac-D,L-Met--NH.sub.2 4.3 g/l Yeast extract 4.5 g/l Peptone from casein 19.7 g/l Glucose 18.4 g/l KH.sub.2 PO.sub.4 0.5 g/l K.sub.2 HPO.sub.4 2.0 g/l NaCl 1.0 g/l CaCl.sub.2 *2 H.sub.2 O 0.05 g/l MgSO.sub.4 *7 H.sub.2 O 0.1 g/l Vitamin solution according to Schlegel* 2.5 ml/l Trace saline solution 0.8 ml/l (Agar in the case of solid media 18.0 g/l)______________________________________ *Schlegel, H. G. (1985): Allgemeine Mikrobiologie [German General Microbiology], Thieme Verlag, Stuttgart
Trace saline solution H.sub.3 BO.sub.3 75.0 mg MnCl.sub.2 *4H.sub.2 O 50.0 mg ZnCl.sub.2 187.0 mg CuSO.sub.4 *5H.sub.2 O 50.0 mg FeCl.sub.3 *6H.sub.2 O 625.0 mg (NH.sub.4).sub.6 Mo.sub.7 O.sub.24 *4H.sub.2 O 25.0 mg COCl.sub.2 *6H.sub.2 O 37.50 mg NiCl.sub.2 *6H.sub.2 O 50.00 mg H.sub.2 O ad 0.2 l______________________________________
1.2 Cellular maceration
The cell maceration took place by the wet grinding of a 20-40% cellular suspension in 50 mM tris/HCl buffer, pH 7.5 with glass beads .O slashed.0.3 mm. The glass beads and the cellular fragments were separated by centrifugation. The glass beads were then re-suspended in 50 mM tris/HCl, pH 7.5 and separated again by centrifugation. The supernatants were purified and constituted the raw extract for the workup described in the following. The cellular maceration was evaluated by determining the amount of protein released according to Bradford (Bradford, M. M. (1976), Anal. Biochem., 72, 248-254) and by microscopic observation.
1.3 Purification
1.3.1. Ion Exchange Chromatography
As the first step in the purification of the peptide amidase from Xanthomonas maltophilia an anion exchange chromatography was carried out on Q-sepharose Fast Flow (Pharmacia, Uppsala). The following conditions applied for the anion exchanger:
______________________________________Column 10 cm * 0 * 1.3 * 1.3 * cm.sup.2 = 53 ml Q sepharose FF (Pharmacia, Uppsala) Travel rate 10 ml/min Equilibration 50 mM tris, 20 mM KCl, pH 8.0 Specimen charging 77.2 ml raw extract a 6.8 mg BSAeq/ml Washing 50 mM tris/HCl, 20 mM KCl, pH 8.0 Elution Linear gradient with rising salt content 200 ml 50 mM tris, 20 mM KCl, pH 8.0 20 ml 50 mM tris, 200 mM KCl, pH 8.0______________________________________
The detection took place at 280 nm, the fractions were trapped at 10 ml each. The peptide amidase was able to be eluted at a salt content of 80-120 mM KCl from the anion exchanger. The active fractions were pooled and concentrated with the aid of an Amicon ultrafiltration cell with a YM 10 membrane to 2 ml for the following gel filtration.
1.3.2 Gel filtration
The active fractions of the anion exchange chromatography were concentrated as described and subjected to a gel filtration on Superdex G 75 material (Pharmacia, Uppsala). The following conditions applied for the gel filtration:
______________________________________Column 60 cm * 0 * 0.8 * 0.8 * cm.sup.2 = 120.6 ml Travel rate 1 ml/min Equilibration 50 mM tris, 150 mM KCl, pH 7.5 Specimen 2 ml a 4.55 mg BSAeq/ml of the concentrated active fractions of the anion exchange chromatography Elution 50 mM tris, 150 mM KCl, pH 7.5 Fraction size 1 ml Detection 280 nm______________________________________
The active fractions of the gel filtration were pooled and concentrated via a YM 10 membrane in an Amicon ultrafiltration cell to 1 ml (1.47 mg BSAeq/ml) and were available in this manner for the following isoelectric focusing.
1.3.3 Isoelectric Focusing
The active fractions of the gel filtration and those of the gel filtration evaporated to 1 ml as described under 1.3.2 were purified with the aid of isoelectric focusing. The conditions for this are presented in the following.
______________________________________Column 5.1 cm * 0.25 * 0.25 * cm.sup.2 * 0 = 1 ml Mono P (Pharmacia, Uppsala) Travel rate 1 ml/min Equilibration 25 mM triethanol amine, pH 8.0 Specimen 1 ml of the concentrated active fractions of the gel filtration (re-buffered with 25 mM triethanol amine, pH 8.0, 1.47 mg BSAeq/ml) Washing 25 mM triethanol amine, pH 8.0 Elution 10 mM linear pH gradient from A to B Eluent A: 25 mM triethanol amine, pH 8.0 Eluent B: Polybuffer 74 (diluted 1:10, Pharmacia), pH 5.0 Fractions 0.5 ml Detection 280 nm______________________________________
In the first two steps of the purification (anion exchange chromatography and gel filtration) interfering protease/peptidase activities were completely removed. After the isoelectric focusing a preparation enriched 533-fold was obtained. A main band is observed in the native gel which band is enzymatically active. The N-terminal sequence was determined after elution of the band out of the native gel by means of a liquid-phase sequenator (Applied Biosystems 470 with on-line HPLC coupling).
EXAMPLE 2
Characterization of the Enzyme
pH Optimum and pH Stability
FIG. 1 shows the dependency of the conversion rate in % on the pH. 50 mM Mc-Ilvain buffer were used in the pH range of 3.0-7.25, 50 mM tris/HCl buffer between pH 7.0-9.0 and for the basic pH range of 9.5-10.5 50 mM Na.sub.2 CO.sub.3 buffer. The test batch of 1 ml was composed as follows:
______________________________________100 .mu.l 100 mM Z--Gly--Tyr--NH.sub.2 (dissolved in H.sub.2 O/dimethylformamide in a 1:1 ratio) 200 .mu.l Enzyme solution a 63 .mu.g BsAeq/ml of the purification stage after the gel filtration 700 .mu.l Buffer.______________________________________
A pre-incubation took place without the addition of substrate for 5 min at 30.degree. C. The reaction was then started by adding 100 .mu.l substrate and incubated 4 hours at 30.degree. C. In order to stop the reaction 100 .mu.l of the reaction batch were removed and compounded with 100 .mu.l glacial acetic acid as well as 1.4 ml HPLC mobile solvent (see 1.4 standard assay of peptide amidase).
FIG. 1 shows the results of the analysis of the pH optimum. The pH optimum of the peptide amidase peptide amidase from Xanthomonas maltophilia results at 6.0 . . . [illegible - "-6"?]0.5.
The relative activity (%) as a function of the time was determined for the pH stability of peptide amidase from Xanthomonas maltophilia. 50 mM Kp.sub.i buffer was used for the pH range of 5.0-7.0 and 50 mM tris/HCl buffer between 7.0-9.0. For the analyses of pH stability 100 .mu.l enzyme solution a 0.73 mg BSAeq/ml (purification stage after the gel filtration) were incubated with 900 .mu.l buffer of differing pH at 30.degree. C. Specimens were drawn at different times and the activity determined with Z-Gly-Tyr-NH.sub.2 as substrate. The results are shown in FIG. 2. A good stability results in the range of pH 7-pH 8.
EXAMPLE 3
Temperature Optimum and Temperature Stability
The temperature optimum of peptide amidase from Xanthomonas maltophilia was determined. To this end 200 .mu.l enzyme solution a 63 .mu.g BSAeq/ml of the purification stage after the gel filtration were compounded with 700 .mu.l of the 50 mM tris/HCl buffer pre-tempered to the particular temperature and the reaction started with 100 .mu.l Z-Gly-Tyr-NH.sub.2 (10 mM in the test batch). Aliquots of 100 Ml were stopped after 2 h with 100 .mu.l glacial acetic acid and the activity determined corresponding to 1.4. The result is shown in FIG. 3. The temperature optimum was approximately 35-40.degree. C. at a pH of 7.5.
The relative activity (%) as a function of the time (h) was determined for the temperature stability of peptide amidase from Xanthomonas maltophilia. To this end 100 .mu.l enzyme solution a 0.73 mg [sic] BSAeq/ml were compounded with 900 .mu.l pre-tempered 50 mM tris/HCl buffer and incubated at 20, 30, 37 and 56.degree. C. Specimens were drawn at different times and the activity determined with Z-Gly-Tyr-NH.sub.2 as substrate. The results are shown in FIG. 4. Whereas the enzyme is inactivated at 56.degree. C. after a few minutes already, it proves to be extremely stable at 20, 30 and 37.degree. C.
EXAMPLE 4
Enzyme Kinetics of Peptide Amidase
The dependency of the reaction rate of peptide amidase from Xanthomonas maltophilia on the substrate concentration (Z-Gly-Tyr-NH.sub.2) was determined and the kinetic parameters determined from the data according to Marquardt. To this end 50 .mu.l enzyme solution a 27 .mu.g BSAeq/ml were compounded with 400 .mu.l 50 mM tris/HCl buffer, pH 7.5. The reaction was started by adding Z-Gly-Tyr-NH.sub.2 as substrate. The substrate was present in the reaction batches in a concentration range of 0.4 to 20 mM. The incubation took place for 2 hours at 30.degree. C. The enzyme activity was then determined as described under 1.4. The K.sub.m value was determined with 0.82 mM and v.sub.max with 0.53 U/mg BSAeq.
FIG. 5 shows the reaction rate of the deamidation of Z-Gly-Tyr-NH.sub.2 as a function of the substrate concentration.
1.4 Standard Assay of Peptide Amidase
The reaction conditions were selected with a view to the pH stability of peptide amidase from Xanthomonas maltophilia.
Standard Assay of Peptide Amidase
______________________________________50 mM tris/HCl, pH 7.5 350-700 .mu.l Enzyme solution 100-200 .mu.l 100 mM Z--Gly--Tyr--NH.sub.2 dissolved in buffer/DMF 1:1 (10 mM in the test) 50-100 .mu.l Test batch 500-1000 .mu.l Temperature 30.degree. C. Incubation time variable______________________________________
In order to stop the reaction 100 .mu.l of the reaction solution were removed, compounded with 100 .mu.l glacial acetic acid and filled with 1.4 ml HPLC mobile solvent. An aliquot of 20 .mu.l was analyzed by HPLC. The conditions for the HPLC analysis of Z-Gly-Tyr-NH.sub.2 are cited in the following:
______________________________________Mobile solvent: 65% 10 mM TBA (tetrabutyl ammonium sulfate) 35% acetonitriie Travel rate 1 ml/min Travel time 10 min Detection 280 nm Elution isocratic Column RP-18, ODS Hypersil (5 .mu.m) Retention times Z--Gly--Tyr--NH.sub.2 4.5 min Z--Gly--Tyr--OH 5.9 min______________________________________
EXAMPLE 5
Substrate Spectrum
18 mU of peptide amidase (purification state after the gel filtration) per ml test batch were used for the substrate spectrum of peptide amidase from Xanthomonas maltophilia. The concentration of the tested substrates was 10 mM in the reaction batch. As far as not otherwise indicated, L-amino acid derivatives were used. The incubation took place in 50 mM tris/HCl, pH 7.5 at 30.degree. C. for 3 hours. The reaction was stopped by being heated for 5 minutes at 95.degree. C. The determination of activity took place with enzymatic determination of the released ammonia (Bergmeyer, U. (1985): Methods of Enzymatic Analysis, p. 459, VCH Verlagsgesellschaft, Weinheim). Table 4a shows the conversion of dipeptide amides, table 4b the conversion of N-acetylamino acid amides and table 4c the influence of the N-terminal protective groups and of the amino acid adjacent to the C terminus.
The following thin-layer chromatographic methods were used for the analysis of the substrates and products cited in table 4d. To this end 1 .mu.l of the stopped reaction batch was applied.
______________________________________Stationary phase DC aluminum foil 60 F.sub.254 (20 * 10 cm.sup.2) Mobile phase Pyridine/butanol/glacial acetic acid/water (12:15:3:5) Detection Ninhydrin (0.3% in propan-1-ol) The color development took place for approximately 3 min at 100.degree. C.)______________________________________
The following HPLC separating conditions applied for the analysis of the conversion of longer-chain peptides shown in table 4e:
______________________________________ Retention time Mobile amide acid Wavelength Substrate solvent* (min) (nm)______________________________________Z--Pro--Leu--Gly--NH.sub.2 60/40 6.0 7.3 256 Z--Gly--Gly--Leu--NH.sub.2 60/40 4.9 6.0 220 Gly-D-Phe--Tyr--NH.sub.2 80/20 3.8 4.4 280 Leu-encaphaline amide 80/20 6.1 7.6 220______________________________________ *10 mM tetrabutylammonium sulfate/acetonitrile
In addition, the presence of possible protease- or peptidase activity was tested for with the aid of thin-layer chromatography. No release of amino acids could be detected for any of the peptides.
TABLE 4a______________________________________Conversion of dipeptide amides Substrate Relative conversion (10 mM) (%)______________________________________Ala--Gly--NH.sub.2 39 Phe--Gly--NH.sub.2 51 Tyr--Gly--NH.sub.2 54 Leu--Gly--NH.sub.2 54 Gly--Gly--NH.sub.2 8 Val--Gly--NH.sub.2 22 Pro--Gly--NH.sub.2 66 Gly--Tyr--NH.sub.2 174 Phe--Ala--NH.sub.2 203 Ala--Ala--NH.sub.2 211 Leu--Ala--NH.sub.2 217 Gly--Phe--NH.sub.2 214 Tyr--Phe--NH.sub.2 190 Ser--Phe--NH.sub.2 217 Ala--Phe--NH.sub.2 218 Leu--Phe--NH.sub.2 203 Val--Phe--NH.sub.2 140 His--Phe--NH.sub.2 137 Pro--Phe--NH.sub.2 158 Tyr--Pro--NH.sub.2 0 Ala--Asn--OH 0 Gly--Asn--OH 0 Ala--Gln--OH 0______________________________________
TABLE 4b______________________________________Conversion of N-acetyl amino acid amides Substrate Relative conversion (10 mM) (%)______________________________________Ac--Ala--NH.sub.2 182 Ac--Val--NH.sub.2 1 Ac--Ile--NH.sub.2 6 Ac-D,L-neopentylglycine 131 amide Ac--Pro--NH.sub.2 0 Ac--Cys--NH.sub.2 82 Ac-D,L-Met--NH.sub.2 102 Ac--Ser--NH.sub.2 58 Ac--Thr--NH.sub.2 21 Ac--Phe--NH.sub.2 134 Ac--Tyr--NH.sub.2 123 Ac--Phg--NH.sub.2 * 28 Ac--Trp--NH.sub.2 157 Ac--Nal--NH.sub.2 * 84 Ac--Lys--NH.sub.2 175 Ac--Arg--NH.sub.2 110 Ac--His--NH.sub.2 177 Ac--Glu--NH.sub.2 162______________________________________ Phg = phenylglycine Nal = naphthylalanine
TABLE 4c______________________________________Influence of the protective group and of adjacent amino acid on the deamidation of the C terminus Substrate Relative conversion (10 mM) (%)______________________________________Ac--Tyr--NH.sub.2 123 Bz--Tyr--NH.sub.2 173 Gly--Tyr--NH.sub.2 174 Phe--Ala--NH.sub.2 203 Ala--Ala--NH.sub.2 211 Leu--Ala--NH.sub.2 217 Z--Ala--NH.sub.2 62 Z-D-Ala--NH.sub.2 0 N-Methoxy-D,L-Met--NH.sub.2 109 N-Ethoxy-D,L-Met--NH.sub.2 124 N-Carbamoyl-D-L-Met--NH.sub.2 77 N-Acetyl-D,L-Met--NH.sub.2 102 Arg--Met--NH.sub.2 125______________________________________
TABLE 4d______________________________________Enzymatic conversion of unprotected amino acid amides Substrate (10 mM) Conversion______________________________________H--Ala--NH.sub.2 0 H--arg--NH.sub.2 0 H--Leu--NH.sub.2 0 H--Tyr--NH.sub.2 0 H--Met--NH.sub.2 0 H--Phe--NH.sub.2 0 H--Lys--NH.sub.2 0 H--Val--NH.sub.2 0 H--Ile--NH.sub.2 0 H--Thr--NH.sub.2 0 H--Trp--NH.sub.2 0 H--Ser--NH.sub.2 0 H-D-Ala--NH.sub.2 0 H-D-Leu--NH.sub.2 0______________________________________
TABLE 4e______________________________________Enzymatic conversion of longer-chain peptides Substrate Relative conversion (10 mM) (%)______________________________________Z--Pro--Leu--Gly--NH.sub.2 50 Z--Gly--Gly--Leu--NH.sub.2 6 Gly--Phe-D-Phe--NH.sub.2 0 Gly-D-Phe--Tyr--NH.sub.2 33 Leu-encephaline amide 52______________________________________
The results show that with the exception of L-Pro, all proteinogenous, protected amino acid amides and peptide amides are deamidated. Even a few protected, non-proteinogenous amino acid amides are hydrolyzed (phenylglycine, naphthylalanine, neopentylglycine). D-amino acids in the C-terminal position are not converted. The amide function in the side chains of asparagine and glutamine are not attacked. The peptide bonds of longer-chain oligopeptides are not split, unprotected amino acid amides are not converted.
EXAMPLE 6
Splitting of Racemic Mixtures of N-protected Amino Acid Amides
The examinations for the splitting of racemic mixtures took place in 50 mM triethylammonium carbonate buffer, pH 7.5. The test batches a 50 ml with 20 U peptide amidase each were incubated at 30.degree. C. Z-D,L-Ala-NH.sub.2, Ac-D,L-Met-NH.sub.2 and Cc-D,L-neopentylglycine amide (Ac-D,L-Npg-NH.sub.2) were available as substrates. The concentration of the substrates in the reaction batch was 10 mM. Specimens were taken at different times, the reaction stopped by heating for 5 minutes at 95.degree. C. and the enantiomeric purity examined with HPLC. The results are shown in the following:
______________________________________Z-D-Ala--OH 0.4% Z-L-Ala--OH 99.6% Ac-D-Met--OH 0.2-0.3% Ac-L-Met--OH 99.7-99.8% Ac-D-Npg--OH 0.2% Ac-L-Npg--OH 99.8%.______________________________________
The results are also explained by FIG. 6, which refers to the splitting of racemic mixtures of Z-D,L-Ala-NH.sub.2, and by FIG. 7, which shows the enantioselective deamidation of N-Ac-D,L-Met-NH.sub.2
EXAMPLE 7
Influence of Enzyme Effectors on the Peptide Amidase Activity
The examinations took place in 50 mM tris/HCl, pH 7.5. After a preincubation of the enzyme (38 mU per batch, purification stage after the gel filtration) with the effector (10 mM in the test batch) for 1 h at 30.degree. C. the reaction was started by adding substrate (Z-Gly-Tyr-NH.sub.2, 10 mM in the test batch). The reaction batches were incubated for 2.5 h at 30.degree. C. Table 5 shows the results of the influence of enzyme effectors on the peptide amidase activity. It is apparent that peptide amidase belongs neither to the classic serine hydrolases which are inhibited at a concentration of PMSF of 1 mM or of Pefabloc of 0.2 mM already nor to the metalloenzymes which are inhibited by EDTA or 1.10-phenanthroline in the concentration range indicated here.
TABLE 5______________________________________Enzymatic activity in the presence of potential inhibitors Potential inhibitor residual (10 mM in the test) activity (%)______________________________________CUSO.sub.4 *5 H.sub.2 O 103 COCl.sub.2 *6 H.sub.2 O 80 NiCl.sub.2 *6 H.sub.2 O 93 HgCl.sub.2 *6 H.sub.2 O 67 EDTA 96 1,10-phenanthroline 92 2,2'-dipyridyl 97 D-cycloserine 100 Semicarbazide 99 1,4-dithio-D,L-threitol (DDT) 96 Actinonine 106 Phenylmethane sulfonyl fluoride 58 (PMSF) 4-(2-aminoethyl)-benzylsulfonyl fluoride (Pefabloc) 10.0 mM 0 0.3 mM 62 0.1 Mm 82______________________________________
EXAMPLE 8
Influence of Solvents on the Peptide Amidase Activity and Stability of Peptide Amidase During Incubation in Solvent
200 .mu.l enzyme solution (59 .mu.g BSAeq/ml, purification stage after the gel filtration) were compounded in each instance with 700 .mu.l of an appropriate mixture of 50 mM tris/solvent, pH 7.5 for the examinations of the influence of solvents on the peptide amidase activity. Dimethylformamide (DMF), acetone, ethanol and propan-1-ol, which were present in the reaction batch up to 70% by volumetric amount, were tested as solvent. The reaction was started by adding substrate Z-Gly-Tyr-NH.sub.2. The incubation took place for 90 minutes at 30.degree. C. Then, aliquots of 100 .mu.l of the reaction batches were provided with 100 .mu.l glacial acetic acid and the enzyme activity determined as described in 1.4. FIG. 8 shows the results of the influence of solvents on the enzyme activity. It is apparent that at 20% DMF 94% residual activity is still present and even at 30% 59% is still present. In the presence of other solvents such as propan-2-ol the enzyme distinctly looses activity but is nevertheless not completely inactivated at a content of 10% (residual activity 30%).
In order to determine the solvent stability of peptide amidase from Xanthomonas maltophilia 600 .mu.l enzyme solution a 57 .mu.g BSAeq/ml (purification state after the gel filtration) were compounded with 150 .mu.l solvent and, as control, 150 .mu.l 50 mM tris/HCl, pH 7.5. The incubation took place at 30.degree. C. Specimens for the determination of activity were drawn at different times. Dimethylformamide (DMF), acetone, ethanol and propan-l-ol were tested as solvent. FIG. 9 shows the solvent stability of peptide amidase from Xanthomonas maltophilia. After 26 hours a residual activity of 32% still results at a solvent content of 20% DMF.
EXAMPLE 9
Determination of the Molar Mass
The relative molar mass of peptide amidase from Xanthomonas maltophilia was determined by gel filtration (travel conditions see 1.3.2). The following calibration proteins were used.
______________________________________ Molecular weight V.sub.e K.sub.AV (daltons) (ml) (-)______________________________________Ribonuclease A 13700 85.6 0.53 Chymotrypsinogen 25000 77.9 0.42 Ovalbumin 43000 65.7 0.26 Bovine serum 67000 58.6 0.16 albumin Blue dextran 2000000 26.4 0.00 2000______________________________________
The detection took place at 280 nm. The elution volume of the peptide amidase was determined by determination of activity. The relative molar mass was determined from the elution volume, using the calibration curve, at 38000.+-.1000 daltons.
EXAMPLE 10
Inducibility of Peptide Amidase from Xanthomonas maltophilia
1 l Erlenmeyer flasks were provided with 200 ml of the nutrient medium used in the second part of the screening for the examinations of the inducibility of peptide amidase from Xanthomonas maltophilia. The amount of yeast extract was raised to 0.1% thereby and only one amide derivative added to 0.5% of the medium in each instance. In addition, media without the addition of amides and with 1.5% yeast extract were examined. Ac-DL-Met-NH.sub.2, leucine amide and carnitine amide were used as amides. The flasks were inoculated to 0.5% and agitated 2 days at 30.degree. C. and 120 rpm. The obtention of the raw extracts took place as already described above. Table 6 shows the results. It is apparent from the data at the enzyme is formed even without the addition of Ac-DL-Met-NH.sub.2 as inductor in the cell but that the specific activity can be doubled to tripled by the addition of this inductor. On the other hand, the addition of other amides shows no influence.
Table 6 Induction of Peptide Amidase from Xanthomonas maltophilia
______________________________________ Protein Spec. content activity Activity (mg (mU/mg Additives (mU/ml) BSAeq/ml) BSAeq)______________________________________Without 29 6.62 4 additive 1.5 yeast 58 8.29 7 extract Ac-DL--Met--NH.sub.2 88 6.65 13 Leu--NH.sub.2 15 5.22 3 Carnitine amide 30 7.13 7______________________________________
EXAMPLE 11
Preparation of Racemic, N.sub..alpha. -protected Amino Acid Amides for the Enzymatic Separation with Peptide Amidase
A) N.sub..alpha. -formyl-DL-methionine amide
30 g (0.20 mole) DL-methionine amide were agitated with 250 ml methyl formate for two days at room temperature, during which fine, slightly yellow crystals developed. They were filtered off and recrystallized out of a mixture of 150 ml hexane and 160 ml ethanol. After cooling off, filtering, washing and drying, 23 g (55%) N.sub..alpha. -formyl-DL-methionine amide were obtained in the form of colorless crystals with a melting point of 121-122.degree. C.
B) N.sub..alpha. methylaminocarbonyl-DL-methionine amide
18 ml (0.3 mole) methylisocyanate were dripped into a solution of 30 g (0.2 mole) DL-methionine amide in 350 ml water at 5-10.degree. C., during which a colorless, crystalline precipitate formed. After 30 min of subsequent agitation at 5-10.degree. C. and 30 min at room temperature the crystals were filtered off, washed with water and dried, yielding 25 g product. A concentrating of the mother liquor yielded a further 10 g. 29 g (70%) N.sub..alpha. methylaminocarbonyl-DL-methionine amide in the form of light, flaky crystals with a melting point of 156-157.degree. C. were obtained by recrystallization out of methanol/acetic ester.
C) N.sub..alpha. -methoxycarbonyl-DL-methionine amide
85 ml (1.11 moles) methylchloroformate were dripped into a solution of 150 g (1.02 moles) DL-methionine amide in 200 ml water at 5-10.degree. C., during which the pH was maintained at 8-10 by the addition of sodium hydroxide solution. After 30 min of subsequent reaction 60 ml water were added, whereupon crystals formed which were filtered off, washed with water and dissolved in 250 ml water. This solution was extracted twice and the crystallization mother liquor extracted once with 500 ml methylene chloride in each instance. After rotating in, 162 g yellowish, crystalline residue remained. It was dissolved in 200 ml hot ethanol. Then, 400 ml MTBE were added and after the appearance of the first colorless crystals another 200 ml MTBE. After cooling in an ice bath, filtering off, washing with 200 ml MTBE and drying, 127 g (60%) N.sub..alpha. -methoxycarbonyl-DL-methionine amide with a melting point of 93-94.degree. C. were obtained.
D) N.sub..alpha. -ethoxycarbonyl-DL-methionine amide
106 ml (1.10 moles) ethylchloroformate were dripped into a solution of 150 g (1.02 moles) DL-methionine amide in 200 ml water at 5-10.degree. C., during which the pH was maintained at 7-9 by adding sodium hydroxide solution. A thick, finely crystalline precipitate rapidly formed. A suspension which was just able to still be agitated was obtained by the addition of 800 ml water which suspension was agitated 3 hours further at room temperature. Then the colorless crystals were filtered off, washed with water and recrystallized out of 900 ml water. After cooling to 0-5.degree. C., filtering off, washing with water and drying, 129 g (57%) N.sub..alpha. ethoxycarbonyl-DL-methionine amide with a melting point of 110-112.degree. C. were obtained.
E) N.sub..alpha. -benzyloxycarbonyl-DL-methionine amide
51 ml benzyloxycarbonyl chloride were dripped into a solution of 50 g (0.34 mole) DL-methionine amide in 200 ml water at 5-20.degree. C., during which the pH was maintained at 7-9 with sodium hydroxide solution. A slimy precipitate formed immediately which became finely crystalline upon the addition of 200 ml MTBE. After the end of the addition the mixture was agitated 30 min further at room temperature. The precipitated, colorless crystals were then filtered off, washed with a little MTBE and recrystallized out of 700 ml toluene. After filtering off, washing with toluene and drying, 67 g (69%) Na benzyloxycarbonyl-DL-methionine amide with a melting point of 120-122.degree. C. were obtained.
F) N.sub..alpha. -acetyl-DL-neopentylglycine amide
12 ml (0.13 mole) acetic anhydride were dripped into a solution of 17 g (0.12 mole) DL-neopentylglycine in 200 ml water under ice cooling in approximately 30 min, during which the pH was maintained at approximately 8 with sodium hydroxide solution. After 1 h agitation at room temperature an extraction was performed three times with 100 ml methylene chloride and the organic phase rotated in after drying over sodium sulfate. 20 g (89%) N-acetyl-DL-neopentylglycine remained as colorless solid.
Then, 14 ml (0.1 mole) triethylamine were dripped into 19 g (0.1 mole) N-acetyl-DL-neopentylglycine in 150 ml THF at -10.degree. C. in 15 min. After 10 min a solution of 10 ml (0.1 mole) ethylchloroformate in 10 ml THF was added dropwise in such a manner that the temperature did not exceed -5.degree. C. Then, 70 ml 25% ammonia solution were added all at once, then 50 ml THF and then the mixture was agitated 2 h at -5.degree. C. and overnight at room temperature. The batch was then evaporated to dryness, thoroughly agitated with 100 ml water, the solid filtered off and recrystallized out of 70 ml methanol. A total of 15 g (78%) N.sub..alpha. -acetyl-DL-neopentylglycine amide were obtained in the form of colorless crystals with a melting point >205.degree. C.
G) N.sub..alpha. -benzyloxycarbonyl-DL-neopentylglycine amide
15 ml (0.11 mole) benzyloxycarbonylchloride were dripped into a solution of 15 g (0.10 ml) DL-neopentylglycine in 150 ml water under ice cooling in approximately 30 min, during which the pH was maintained at approximately 9 with sodium hydroxide solution. After 1 h agitation at room temperature an extraction was carried out three times with 75 ml methylene chloride and the organic phase rotated in after drying over sodium sulfate. 25 g (90%) N-benzyloxycarbonyl-DL-neopentylglycine remained as a colorless oil which crystallized upon standing.
Then, 12 ml (0.90 mole) triethylamine was dripped into 24 g (0.09 mole) N-benzyloxycarbonyl-DL-neopentylglycine in 150 ml THF at -10.degree. C. in 15 min. After 10 min a solution of 8 ml (0.09 mole) ethylchloroformate in 10 ml THF was added dropwise in approximately 30 min in such a manner that the temperature did not exceed -5.degree. C. After 30 min agitation at -5.degree. C. 60 ml 25% ammonia solution were added all at once and the mixture then agitated 2 h at -5.degree. C. and overnight at room temperature. The batch was then evaporated to dryness, taken up with 50 ml water and extracted with 150 ml methylene chloride. After drying of the organic phase over sodium sulfate and rotating in, 26 g residue remained which was dissolved in 50 ml methanol and then compounded with 70 ml water within approximately 2 h under ice cooling. After filtration, washing with methanol/water and drying, 13 g (54%) N.sub..alpha. benzyloxycarbonyl-DL-neopentylglycine amide were obtained as a colorless solid with a melting range of 132-137.degree. C.
EXAMPLE 12
Preparation of D-neopentylglycine from N-acetyl-D,L-neopentylglycine amide
10 mM N-acetyl-D,L-neopentylglycine amide were incubated with 20 U peptide amidase in a 50 ml Erlenmeyer flask in 50 mM triethylammonium carbonate buffer at pH 7.5 and 30.degree. C. The conversion was controlled by HPLC. After 24 hours the conversion was 50% and did not change any more as time passed. The enzyme was now deactivated by five minutes of heating and the enantiomeric purity examined. The purity of N-acetyl-L-neopentylglycine (determined by ligand exchange chromatography) was 99.8% and the purity of the N-acetyl-D-neopentylglycine amide (determined by inclusion chromatography) was 99.7%. The two products were separated by anion exchange chromatography on Amberlite M 500 and the N-acetyl-D-neopentylglycine amide converted by several hours of hydrolysis in 6-normal, boiling hydrochloric acid into the free D-amino acid, during which the demonstration of the complete conversion by HPLC or DC takes place. The amount of rotation of the D-neopentylglycine [.alpha..sup.25.sub.D ] (c=0.5, 6N HCl) was -16.2.degree..
Methods Used for the Separation of Enantiomers
The enantiomers of the remaining N-acyl-amino acid amide were separated from each other by inclusion chromatography and the two enantiomers of the N-acyl amino acid product by ligand exchange chromatography.
__________________________________________________________________________# SEQUENCE LISTING - - - - (1) GENERAL INFORMATION: - - (iii) NUMBER OF SEQUENCES: 1 - - - - (2) INFORMATION FOR SEQ ID NO:1: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 17 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: peptide - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:1: - - Xaa Arg Asn Val Pro Phe Pro Tyr Ala Glu Th - #r Asp Val Ala Asp 1 5 - # 10 - # 15 - - Leu Gln__________________________________________________________________________

Number	Name	Date	Kind
5215897	Sakashita	Jun 1993
5238838	Kula	Aug 1993

Peptide amidase from xanthomonas

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Nawaz et al., Can. J. Microbiol., 1993, 39(2), 207-12.
Stelkes-Ritter, et al., "Characterization of a Newly Screened Microbial Peptide Amidase", Proceedings of the 5th Akabori Conference, May 1994, pp. 9-12.