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Sulfoxides, Analogues of L-Methionine and L-Cysteine As Pro-Drugs against Gram-Positive and Gram-Negative Bacteria
N. V. Anufrieva1, E. A. Morozova1, V. V. Kulikova1, N. P. Bazhulina1, I. V.Manukhov2, D. I. Degtev2, E. Yu. Gnuchikh2, A. N. Rodionov1, G. B. Zavilgelsky2, T. V. Demidkina1* 1Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Vavilova Str., 32, Moscow, 119991, Russia
2State Research Institute of Genetics and Selection of Industrial Microorganisms, 1-st Dorozhniy pr.,
1, Moscow, 117545, Russia
*E-mail: [email protected], [email protected]
Copyright © 2015 Park-media, Ltd. This is an open access article distributed under the Creative Commons Attribution License,which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
ABSTRACT The problem of resistance to antibiotics requires the development of new classes of broad-spectrum antimicrobial drugs. The concept of pro-drugs allows researchers to look for new approaches to obtain effective drugs with improved pharmacokinetic and pharmacodynamic properties. Thiosulfinates, formed enzymatically from amino acid sulfoxides upon crushing cells of genus Allium plants, are known as antimicrobial compounds. The instability and high reactivity of thiosulfinates complicate their use as individual antimicrobial compounds. We propose a pharmacologically complementary pair: an amino acid sulfoxide pro-drug and vitamin B6 - dependent methionine y-lyase, which metabolizes it in the patient's body. The enzyme catalyzes the y- and P-elimination reactions of sulfoxides, analogues of L-methionine and L-cysteine, which leads to the formation of thiosulfinates. In the present work, we cloned the enzyme gene from Clostridium sporogenes. Ionic and tautomeric forms of the internal aldimine were determined by lognormal deconvolution of the holoenzyme spectrum and the catalytic parameters of the recombinant enzyme in the y- and P-elimination reactions of amino acids, and some sulfoxides of amino acids were obtained. For the first time, the possibility of usage of the enzyme for effective conversion of sulfoxides was established and the antimicrobial activity of thiosulfinates against Gram-negative and Gram-positive bacteria in situ was shown.
KEYWORDS Pro-drugs, vitamin B6-dependent enzymes, cloning of Clostridium sporogenes methionine y-lyase gene, alliin, allicin, sulfoxides of amino acids, Gram-positive and Gram-negative bacteria.
ABBREVIATIONS PLP - pyridoxal 5'-phosphate, MGL - methionine y-lyase, His-tag - poly-histidine fragment, His-tag MGL - methionine y-lyase with poly-histidine fragment, megL - gene encoding of MGL in Clostridium sporogenes, DTT - dithiothreitol, NADH - reduced form of P-nicotinamide adenine dinucleotide, EDTA - ethyl-enediaminetetraacetic acid.
INTRODUCTION
The development of new antimicrobial agents with a minimal inherent risk of inducing rapid resistance to antibiotics is one of the most pressing issues nowadays. Many potentially effective antimicrobial agents are rapidly degraded in the human body and have high toxicity, preventing their use in the concentrations necessary for treatment. This issue can be resolved through the concept of pro-drugs, compounds that must be metabolized in the body of a patient. This concept has been successfully used in tumor therapy [1].
In the present study, we propose using this approach to create effective antimicrobial therapy using a phar-
macological pair of a pro-drug and a biocatalyst metabolizing it. Recently, we have demonstrated that methionine y-lyase (MGL) [EC 4.4.1.11] from Citrobacter freundii catalyzes the ß-elimination reaction of a nonprotein amino acid, (±)-S-(2-propenyl)-L-cysteinesul-foxide ((±)-alliin), resulting in 2-propene thiosulfinate (allicin), a natural antibiotic [2].
MGL catalyzes the y-elimination reaction of L-me-thionine to produce methylmercaptan, a-ketobutyric acid, and ammonia. The enzyme catalyzes the ß-elim-ination reactions of L-cysteine and its S-substituted derivatives to the corresponding mercaptans, pyruvic acid and ammonia, and the substitution reactions at the
Cp- and C^-atoms of L-cysteine and L-methionine and their analogues [3, 4]:
/
^ RSH+CH3-CH^C"COOH +NH3
RX—CH2-CH2-CH^
,COOH
nh2
o
Y-élimination
\RXH> RSH+R'X'—CHÎ-CHz-CH"'
COOH
h2o
/
RX—CH2-CH,
,COOH
nh2
\ R'X'H
RSH
RSH
Y-substitution
.COOH CH3-C^ II O
P-elimination R'X'—CH2-CH^ P-substitution
NH3
COOH
-nh2
X = S, O or Se;
X' = S or Se
MGL is present in fungi [5], Arabidopsis thaliana [6], in various bacteria, including pathogenic Aeromonas spp. [7], Clostridium sporogenes [8], Porphyromonas gingivalis [9], and pathogenic protozoa Entamoeba histolytica [10] and Trichomonas vaginalis [11]. The enzyme has no counterpart in mammals and, therefore, may be considered as a target in pathogens. This approach was implemented using a suicide substrate of the enzyme. Catalysis of the y-elimination reaction of trifluoromethionine led to the formation of trifluo-romethanethiol, which spontaneously decomposes to thiocarbonyl difluoride, which has an antimicrobial effect on MGL-containing T. vaginalis [12], P. gingivalis [13], and E. histolytica [14]. However, the high toxicity of thiocarbonyl difluoride prohibits the use of trifluo-romethionine as an antimicrobial agent.
Allicin, the most well-known antimicrobial and antitumor component of garlic, accounts for about 70% of all thiosulfinates [15] formed by the P-elimination reaction of alliin, which is catalyzed by PLP-dependent alliinase [EC 4.4.1.4] [16] upon crushing of garlic. The antimicrobial action of allicin and other thiosulfinates formed enzymatically during the crushing of plant cells of genus Allium is largely due to their ability to oxidize the sulfhydryl groups of proteins/enzymes of bacterial cells, whereas animal cells are partially protected by the presence of glutathione [17]. The antimicrobial, anti-inflammatory, antioxidant, and anticarcinogenic effects of organic sulfo-compounds, cell extracts of garlic and onions [18, 19], have been known since ancient times. However, isolated thiosulfinates are not used in medicine due to their high reactivity and, hence, instability. Only allicin has been studied extensively as an individual biologically active compound, and its antitumor, antioxidant, antibacterial, and antifungal properties have been identified [20-22].
MGL ability to catalyze the y- and P-elimination reactions of methionine sulfoxide [23] and alliin [2] to produce thiosulfinates allows one to use the concept of pro-drugs to develop a new antimicrobial agent, using the substrates of the enzyme, alliin and other sulfoxides, as pro-drugs in situ generating thiosulfinates.
Previously, we cloned the C. sporogenes gene (megL) encoding MGL with a polyhistidine fragment (His-tag) at the N-terminus of the polypeptide chain and determined some kinetic characteristics of the recombinant enzyme (His-tag MGL). C. sporogenes MGL catalyzed the y-elimination reaction of L-methionine at a faster rate than the enzyme from C. freundii [24] and showed higher cytotoxic activity against a number of tumor cells [25].
The cleavage of His-tag by thrombin increases the rate of the physiological substrate cleavage by C. sporogenes MGL by 1.5 times. In this study, we cloned the C. sporogenes MGL gene without His-tag. The steady-state kinetic parameters of the y- and P-elimi-nation reactions of a number of well-known substrates and sulfoxides, analogues of cysteine and methionine, and the spectral characteristics of C. sporogenes MGL have been determined. The antibacterial activity of mixtures containing MGLs from C. sporogenes and C. freundii and the sulfoxides of amino acids has been demonstrated in a solid medium. It has been shown that the kinetic parameters of the recombinant PLP-de-pendent MGL make it possible, in principle, to use the enzyme to convert pro-drugs, sulfoxides of amino acids, to thiosulfinates.
MATERIALS AND METHODS
Reagents, enzymes
The following compounds were used in the study: pyridoxal 5'-phosphate, L-methionine, L-cysteine, L-homocysteine, L-norvaline, L-norleucine, L-a-aminobutyric acid, alliin, S-ethyl-L-cysteine, S-ethyl-L-homocysteine, L-alanine, O-acetyl-L-ser-ine, lactate dehydrogenase from rabbit muscle, DTT, NADH, sodium periodate, ethyl bromide (all Sigma, USA); EDTA, protamine sulfate (Serva, USA); lactose (Panreac, Spain); glucose, glycerol, magnesium sulfate, ammonium sulfate, monopotassium phosphate, disodium phosphate ("Reakhim," Russia); yeast extract, tryptone (Difco, USA); DEAE-Sepharose (GE Healthcare, Sweden); O-acetyl-L-homoserine was produced by L-homoserine acetylation as described previously [26]. 2-Nitro-5-thiobenzoic acid was obtained according to [27]. (±)-L-methionine sulfoxide was obtained according to the standard procedure [28]. Synthesis of (±)-S-ethyl-L-cysteine and (±)-S-ethyl-L-homocyst-eine sulfoxides was performed according to [29-31].
Restriction and ligation reactions were carried out with enzymes from Promega (USA). A "working buffer" with pH 8.0, containing 100 mM potassium phosphate, 0.1 mM PLP, 1 mM DTT, and 1 mM EDTA was used.
Escherichia coli strain BL21 (DE3) F- ompT hsdSB gal dcm (DE3) (Novagen) was used to express the C. sporogenes MGL gene. E. coli strain K12 AB2463 - are-cA~ derivative of E. coli K12, has a F-, thr-1 leu-6 proA2 his-4 thi-1 argE3 lacY1 galK2 ara-14 xyl-5 mtl-1 tsx-33 rpsL31 supE44, recA13 genotype. It was used for cloning, production, and storage of the plasmid. C. freundii strain ATCC 21434 from the American Type Culture Collection (USA) was kindly provided by R. S. Phillips. The Staphylococcus aureus strain 015 was kindly provided by Yu. F. Belyi. The plasmid with D-2-hydroxy-isocaproate dehydrogenase was kindly provided by K. Muratore.
Cloning of the C. sporogenes MGL gene The pET28a-megL_sporog plasmid was constructed based on the pET28a plasmid, containing the C. sporogenes megL gene with a polyhistidine fragment (His-tag) and designated as pET28a::megL_s_ HT [24]. The amplicon (megL_sporog), containing the megL gene without His-tag, was obtained by PCR. pET28a plasmid carrying megL with His-tag was used as a template. The primers included the NcoI restriction site (underlines): megL_sporog:5'-CGCG-CGGCAGCCCCATGGAGAA-3'(forward), megL_ sporog:5'-CCGGATCTCAGTGGTGGTGGTG-3' (reverse).
MegL_sporog amplicon was cloned in the pET28a vector by the Ncol and EcoRI sites in the recA- E. coli strain AB2463. The cloning was controlled by sequencing the insert. Transformation was carried out using the E. coli strain BL21 (DE3).
ditions according to Laemmli [34]. The concentration of the purified preparations was determined using a A1%278coefficient of 0.8 [23].
Assay of the enzyme activity and steady-state kinetics parameters
MGL activity during the purification was assayed in the y- and P-elimination reactions by measuring the reduction of NADH absorption at 340 nm (e = 6220 M-1cm-1) at 30 °C to estimate the rate of keto acids formation in the conjugation reaction with D-2-hydroxyisocaproate dehydrogenase (the Y-elimination reaction) or lactate dehydrogenase (the P-elim-ination reaction). The reaction mixtures contained the working buffer, 0.2 mM NADH, 10 units of lactate dehydrogenase or 70 of D-2-hydroxyisocaproate dehydrogenase, 30 mM S-ethyl-L-cysteine, or 30 mM L-methionine. One unit of enzyme activity was defined as the amount of the enzyme that catalyzes the formation of 1.0 ^M/min of pyruvate (or a-ketobutyrate). The specific activity of 95% pure enzyme preparations was 26.8 units/mg for the Y-elimination reaction of L-methionine and 8.32 unit/mg for the P-elimination reaction of S-ethyl-L-cysteine.
Steady-state kinetic parameters for the y- and P-elimination reactions were measured in the same manner by varying the substrates concentrations. The obtained data were processed according to the Michae-lis-Menten equation using the EnzFitter software. Calculations were based on the molecular weight of an enzyme subunit of 43 kDa. Inhibition of the Y-elimination reaction of L-methionine by various amino acids was studied under the conditions described above by varying the concentrations of substrates and inhibitors in the reaction mixture. The values of inhibition constants were determined using the EnzFitter software. The data were processed in Dixon coordinates [35].
Biomass growth and enzyme purification
Cells of E. coli BL21 (DE3), containing the MGL gene without His-tag in the pET28a megL_sporog plasmid, were grown in the "inducing" medium [32] at 37 °C with stirring (180 rpm) for 24 hours. The cells were collected by centrifugation and stored at -80 °C. The cells were destroyed and purified from nucleic acids as described previously [33]. Further purification was carried out by ion exchange chromatography on a column with DEAE-Sepharose equilibrated with the working buffer. The column was pre-washed with the working buffer containing 100 mM KCl. The enzyme was elut-ed with the working buffer containing 500 mM KCl, concentrated and dialyzed against the working buffer. The purity of the preparation was checked by poly-acrylamide gel electrophoresis under denaturing con-
Spectral studies
The absorption spectrum of holoenzyme was recorded at 25 °C on a Cary-50 spectrophotometer (Varian, USA) in the working buffer without PLP. The enzyme concentration was 1.036 mg/mL.
Antimicrobial activity of drugs
Overnight cultures of C. freundii and S. aureus grown in a Luria-Bertani medium (LB-medium) at 37 °C were diluted 100-fold in a LB-medium and grown at 37 °C with constant stirring to an optical density of 0.2-0.3 at 600 nm. The bacterial cultures were plated on solid-medium dishes (LB-agar). Mixtures of MGLs from different sources and sulfoxides of amino acids pre-in-cubated at room temperature for 1 hour were applied to 12 mm filter paper disks placed on the dishes. The
Table 1. Kinetic parameters of the y- and P-elimination reactions*
Substrate C. sporogenes MGL C. sporogenes His-tag MGL** C. freundii MGL*** P. putida MGL****
k ts-1 cat, mM kca/KM, M-1s-1 ' k t cat, s-1' mM kcat/KM, M-1s-1 , k t cat, s-1, KM mM kcat/KM, M-1s-1 , k t cat (s-1) KM mM kcat/KM, M-1s-1 ,
L-Met 21.61 0.60 3.60 X 104 9.86 0.43 2.28 x 104 6.2 0.7 8.85 x 103 48.6 0.90 5.4 x 104
(±)-L-MetO 21.66 11.39 1.90 x 103 8.59 7.89 1.09 x 103 8.12 4.65 1.75 x 103 - - -
S-Et-L-Hcy 21.31 0.24 8.87 x 104 7.05 0.27 2.54 x 104 6.78 0.54 1.25 x 104 33.4 0.27 1.23 x 105
(±)-S-Et-L-HcyO 0.48 0.60 8.0 x 102 - - - - - - - - -
O-Ac-L-Hse 37.26 3.18 1.17 x 104 - - - 2.1 2.91 7.21 x 102 78.0 2.22 3.51 x 104
S-Et-L-Cys 6.53 0.43 1.52 x 104 6.3 0.358 1.76 x 104 5.03 0.17 2.96 x 104 5.79 0.48 1.21 x 104
(±)-S-Et-L-CysO 1.39 0.33 4.21 x 103 - - - - - - - - -
O-Ac-L-Ser 5.31 8.01 6.6 x 102 - - - 2.13 4.28 4.98 x 102 - - -
(±)-Alliin 11.43 1.43 7.99 x 103 - - - 5.9 4.7 1.26 x 103 - - -
*The error did not exceed 10%. **Data from [25]. ***Data from [2, 23, 33]. ****Data from [37].
concentrations of MGLs from C. sporogenes and C. fre-undii and sulfoxides were 10 and 2.5 mg/mL, respectively. The dishes were incubated for 24 hours at 37 °C, and inhibition zones were then measured. The control solutions of the enzymes and the sulfoxides mixtures retained their antibacterial activity for 2 weeks.
Determination of allicin
Allicin, produced in the mixtures containing MGL and alliin, was determined in a reaction with 2-ni-tro-5-thiobenzoic acid. The mixture of MGL and alliin was added to 1 mL of 0.1 mM 2-nitro-5-thiobenzoic acid in a 100 mM potassium-phosphate buffer containing 0.2 mM PLP, pH 8.0. The mixture was incubated for 30 min at room temperature. Allicin molar concentration was calculated by the decrease in absorbance at 412 nm using a molar absorption coefficient of 2-nitro-5-thioben-zoic acid at 412 nm of 28,300 M-1cm-1 [27].
RESULTS AND DISCUSSION
Kinetic parameters of the P- and Y-elimination reactions
Previously [25], we showed that cleavage of His-tag from C. sporogenes MGL by thrombin leads to a 1.5fold increase in the activity of the enzyme in the physiological reaction with L-methionine. In this work, we have determined the parameters of steady-state kinetics of C. sporogenes MGL without His-tag in the Y-elimination reactions of five substrates (L-methio-nine, L-methionine sulfoxide, S-ethyl-L-homocysteine, S-ethyl-L-homocysteine sulfoxide and O-acetyl-L-ho-moserine) and in the P-elimination reactions of four substrates (S-ethyl-L-cysteine, S-ethyl-L-cysteine sulfoxide, O-acetyl-L-serine and alliin). Table 1 summa-
rizes the parameters for MGL from C. sporogenes, for MGLs derived from two other bacterial sources, and C. sporogenes His-tag MGL.
The kcat values for C. sporogenes MGL in the y-elimination reactions of three substrates, L-methionine, S-ethyl-L-homocysteine, and L-methionine sulfox-ide, were 2-3 times higher than for C. sporogenes His-tag MGL. KM values for the first two substrates were close, and the KM value for L-methionine sulfoxide was slightly higher than that for His-tag MGL.
The presence of the His-tag fragment does not affect the kinetic parameters of the P-elimination reaction of S-ethyl-L-cysteine, and KM and kcat values for MGL are almost identical to those for His-tag MGL. In the y- and P-elimination reactions, the elimination of the side-chain groups of the substrates is catalyzed by different acid groups of the enzyme. Presumably, in the case of the P-elimination reaction catalyzed by PLP-dependent lyases, this group is the side group of the lysine residue (Lys210 in C. freundii MGL) which binds the coenzyme [36]. In PLP-dependent y-elimination and y-replacement reactions, this role is attributed to the conservative tyrosine residue (Tyr113 in C. freundii MGL) involved in the stacking interaction with the coenzyme ring [36]. This assumption is confirmed by the data obtained for the mutant form of Pseudomonas putida MGL, in which Tyr114 is replaced with Phe [37]. It has also been shown that the acid/base properties of Tyr113 in C. freundii MGL are regulated by the Cys115/Tyr113/Arg60 triad [2]. Arg60 is located in the mobile N-terminal loop of the enzyme, and the nitrogen atom of the guanidine group is positioned within a hydrogen-bond distance from the hydroxyl group of Tyr113 in the three-dimensional structure of the holoenzyme [38], the structures of MGL com-
plexes with amino acids modeling the Michaelis complex [39], and in the spatial structure of the external aldimine of the enzyme with glycine [40]. The His-tag fragment may affect the conformation of the N-ter-minal loop and, therefore, the relative arrangement of the hydroxyl group of Tyr113 and the guanidine group of Arg60, which, in turn, may affect the pKa value of the hydroxyl group of Tyr113. That may explain the increase in the y-eliminating activity of C. sporogenes MGL compared with His-tag MGL.
Comparison of the enzymes from three bacterial sources (Table 1), P. putida, C. freundii, and C. sporogenes, showed that their affinity for both the physiological substrate and its analogues are almost equal. The efficiency of catalysis in the reaction y-elimination of L-methionine for C. sporogene and P. putida MGLs is close, and the kcat/KM value for C. freundii MGL is somewhat lower. The kinetic parameters of the P-elimination reaction of S-ethyl-L-cysteine are very similar for the three enzymes.
C. sporogenes MGL catalyzes the y-elimination reaction of L-methionine sulfoxide with a catalytic efficiency which is an order of magnitude higher than that in the Y-elimination reaction of S-ethyl-L-homocysteine sulfoxide. The rate of the P-elimination reaction of S-ethyl-L-cysteine sulfoxide, catalyzed by the enzyme, is 15 times lower than the rate of the Y-elimination reaction of L-methionine sulfoxide, but due to the greater affinity of C. sporogenes MGL to this substrate, the overall catalytic efficiency is virtually the same. Among the reactions with amino acids sulfoxides, the enzyme most effectively catalyzes the P-elimination reaction of alliin.
The enzyme from C. sporogenes catalyzes the Y-elimination reaction of L-methionine sulfoxide more effectively than C. freundii MGL (kcat value is 2.5 times higher). The rate of alliin cleavage by C. sporogenes MGL is almost 2 times higher than that of the enzyme from C. freundii, the substrate affinity is 3 times higher, and the efficiency of catalysis is 6.3 times higher.
Amino acids with a linear side chain inhibited the Y-elimination reaction of L-methionine competitively. Table 2 shows the inhibition constants for C. sporogenes, C. freundii, and P. putida MGLs. All of these enzymes demonstrate an increase in binding with an increase in the number of methylene groups in amino acids with linear side chains, which can be attributed to the hy-drophobic nature of the active site of the enzyme from P. putida [41] and C. freundii [38]. The significant increase in the affinity of the enzyme from the three sources then switching from L-norvaline to L-norleu-cine and close values of K for L-norleucine and K for
i M
L-methionine and S-ethyl-L-cysteine may be attributed to the presence of a "pocket" for the amino acid methyl group in the MGL active site.
300
350
400 450 À, nm
500
550
Fig. 1. Absorption spectrum of the holoenzyme C. sporogenes MGL
Table 2. Inhibition of the y-elimination reaction of L-methionine*
Amino acid K, mM i7
C. freundii** C. sporogenes P. putida***
L-Ala 3.4 1.5 5.1
L-Abu 8.3 2.0 8.4
L-Nva 4.7 1.9 3.0
L-Nle 0.6 0.37 0.5
"The error did not exceed 10%. "*Data from [23]. "**Data from [43].
Spectral characteristics of the enzyme
The absorption spectrum of C. sporogenes MGL holoenzyme (Fig. 1) at pH 8.0 is similar to the spectrum of C. freundii MGL [23], with a predominant absorption band of the ketoenamine form of the internal aldimine in the region 422-425 nm (Fig. 1, structure II). Just like C. sporogenes His-tag MGL [24], the spectrum contains an intense absorption band with a maximum in the region 502-505 nm, which is attributed to a quinonoid intermediate in the spectra of PLP-dependent enzyme complexes with amino acids and model compounds [42].
Deconvolution of the holoenzyme spectrum in the region 300-500 nm using lognormal curves was performed according to [23]. Table 3 shows the parameters of the absorption bands obtained after decon-volution. In addition to the ketoenamine form, the
Table 3. Parameters of the absorption spectrum bands of the internal aldimine C. sporogenes MGL
Structure E, eV v x 10-3, cm-1 X, nm e x 10-3, M-1cm-1 W x 10-3, cm-1 P f n, %
II1 2.92 23.53 425.0 10.46 3.58 1.58 0.22 64.7
IF 3.24 26.15 382.4 7.76 4.00 1.37 0.02 7.5
I 3.63 29.28 341.5 9.44 3.65 1.23 0.03 10.0
IIX 3.79 30.56 327.2 10.27 3.47 1.29 0.01 5.6
II2* 4.28 34.55 289.4 5.98 5.06 1.20 0.18
* 4.46 35.99 277.9 6.70 4.70 1.50 0.26
E, electron transition energy; v, wave number; wavelength; e, molar absorption coefficient; W, half-width; p, asymmetry; f, oscillator force; n, contents of tautomers and conformers. The content of PLP in the enzyme is 87.8%. * Experimental information about these bands is insufficient.
Above-line indices (1, 2) correspond to the first and second electron transitions of structure II. Above-line indices (x/) correspond to two conformers of structure II (the conformer with the aldimine group in the plane perpendicular to the pyridine cycle plane and the conformer with the aldimine bond released from the coenzyme ring plane but with retained coupling and a hydrogen bond between the aldimine nitrogen atom and the coenzyme 3'-oxygroup).
Table 4. Inhibition of cell culture by mixtures containing MGL and sulfoxides of amino acids
Amino acid sulfoxide Inhibition zone, mm2
C. freundii MGL C. sporogenes MGL
C. freundii S. aureus C. freundii S. aureus
(±)-Alliin 380 754 254 754
(±)-L-MetO 452 491 177 227
(±)-S-Et-L-CysO 314 491 254 314
(±)-S-Et-L-HcyO 254 415 227 227
internal aldimine (Fig. 1, structure II, e = 10410 M-1s-is represented by minor structures, enol tautomer (Fig. 1, structure I), and two ketoenamine conformers with the aldimine bond perpendicular to the plane of the coenzyme ring (absorption in the region of 380 nm) and with the aldimine bond partly removed from the plane of the ring but retaining its coupling with n-electrons of the cofactor and a hydrogen bond between aldimine nitrogen and the 3'-oxygroup of PLP (absorption in the region 327-328 nm). The ionic form of the internal aldimine and tautomeric equilibrium are almost the same as those for C. freundii MGL. The absorption in the region 502-505 nm requires further investigation.
Fig. 2. Diffusion in agar by the Kirby-Bauer method [44]. The mixture of C. sporogenes MGL (10 mg/ml) and alliin (2.5 mg/ml) in 100 mM potassium phosphate-buffer was applied on the - A) cell culture of C. freundii, B) cell culture of S. aureus
Antimicrobial activity of mixtures of
C. freundii and C. sporogenes MGLs with sulfoxides of amino acids
The antibacterial activity of mixtures of MGLs from two sources and sulfoxides of amino acids was assessed using bacterial cultures of Gram-positive S. aureus and Gram-negative C. freundii (Table 4). All mixtures showed a bacteriostatic effect against Gram-positive and Gram-negative bacteria. The most significant effect was observed for the culture of S. aureus (Fig. 2). The bacteriostatic effect was comparable to the inhibition of bacterial cell growth by kan-amycin. The inhibition zones of kanamycin (0.05 mg) and a mixture comprising 0.04 mg of allicin in the C. freundii culture amounted to 314 and 346 mm2, respectively.
Therefore, the data obtained show that the recombinant enzyme effectively catalyzes the conversion of amino acids sulfoxides into thiosulfinates. This suggests that a pharmacological pair of MGL and a sulfoxide can ensure production of thiosulfinates in the amounts necessary for therapeutic purposes.
CONCLUSIONS
MGL catalyzes the y- and P-elimination reactions of sulfoxides, analogues of methionine and cysteine, with a catalytic efficiency comparable to the efficiency of the y- and P-elimination reactions of these amino acids.
Using a solid medium, we have demonstrated that mixtures of sulfoxides and MGL are promising as antimicrobial agents against Gram-positive and Gram-negative bacteria in situ.
The strongest bacteriostatic effect for the mixture of amino acids sulfoxides and MGL have been observed for Gram-positive bacteria S. aureus, and the bacteri-ostatic effect of allicin produced in situ is comparable with the effect of kanamycin.
The authors thank State Research Institute of Genetics and Selection of Industrial Microorganisms for allowing the use of its facilities to clone Clostridium sporogenes methionine y-lyase gene.
This work was supported by the Russian Science Foundation (project № 15-14-00009).
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