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Kinetic Parameters and Cytotoxic Activity of Recombinant Methionine Y-Lyase from Clostridium tetani, Clostridium sporogenes, Porphyromonas gingivalis and Citrobacter freundii
E. A. Morozova1, V. V. Kulikova1, D. V. Yashin2, N. V. Anufrieva1, N. Y. Anisimova3,
S. V. Revtovich1, M. I. Kotlov4, Y. F. Belyi4, V. S. Pokrovsky3, T. V. Demidkina1*
1Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Vavilova Str., 32, Moscow, Russia, 119991
institute of Gene Biology, Russian Academy of Sciences, Vavilova St., 34/5, Moscow, Russia, 119334
3Blokhin Cancer Research Center, Russian Academy of Medical Sciences, Kashirskoe sh., 24, Moscow, Russia, 115478
4Gamaleya Research Institute of Epidemiology and Microbiology, Gamaleya Str., 18, Moscow, Russia, 123098
*E-mail: [email protected], [email protected] Received 04.03.2013
Copyright © 2013 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 steady-state kinetic parameters of pyridoxal 5’-phosphate-dependent recombinant methionine Y-lyase from three pathogenic bacteria, Clostridium tetani, Clostridium sporogenes, and Porphyromonas gingivalis, were determined in P- and Y-elimination reactions. The enzyme from C. sporogenes is characterized by the highest catalytic efficiency in the Y-elimination reaction of L-methionine. It was demonstrated that the enzyme from these three sources exists as a tetramer. The N-terminal poly-histidine fragment of three recombinant enzymes influences their catalytic activity and facilitates the aggregation of monomers to yield dimeric forms under denaturing conditions. The cytotoxicity of methionine Y-lyase from C. sporogenes and C. tetani in comparison with Citrobacter freundii was evaluated using K562, PC-3, LnCap, MCF7, SKOV-3, and L5178y tumor cell lines. K562 (IC50=0.4-1.3 U/ml), PC-3 (IC50=0.1-0.4 U/ml), and MCF7 (IC50=0.04-3.2 U/ml) turned out to be the most sensitive cell lines.
KEYWORDS kinetic parameters; methionine Y-lyase; pathogenic microorganisms; oligomeric structure; cytotoxicity.
ABBREVIATIONS DTT - dithiothreitol; His-tag - poly-histidine fragment; MGL - methionine Y-lyase; MSC - mesenchymal stromal cells; PLP - pyridoxal 5’-phosphate.
INTRODUCTION
Methionine y-lyase (MGL) [EC 4.4.1.11] is a pyridoxal 5’-phosphate-dependent enzyme that catalyzes the Y-elimination reaction of L-methionine, yielding methyl mercaptan, a-ketobutyric acid, and ammonia:
In addition to the physiological reaction, the enzyme catalyzes the P-elimination reaction of L-cysteine and its S-substituted derivatives, yielding the corre-
sponding mercaptans, pyruvic acid, and ammonia [1]. The enzyme was isolated from Pseudomonas putida, Aeromonas sp., Clostridium sporogenes, Porphyromonas gingivalis, Brevibacterium linens BL2, Citrobacter freundii, and several others, from eukaryotic protozoa Trichomonas vaginalis and Entamoeba histolytica, and from fungi Aspergillus flavipes [2]. This enzyme is absent in mammalian cells but is present in pathogenic bacteria, such as Aeromonas sp. [3], C. sporogenes [4], P. gingivalis [5], and in pathogenic protozoa E. histolytica [6], T. vaginalis [7], which allows one to consider the enzyme as a potential target for novel antibiotics.
The enzyme is of interest as an anticancer agent, since the growth of malignant cells of various origins (unlike the growth of normal cells) is accompanied by obligatory methionine utilization [8]. The possibility of development of an anticancer agent based on MGL from P. putida has been demonstrated in vitro and in vivo [9-12]. Antitumor activity of the enzyme from A. fla-vipes with respect to several human tumors was observed in vivo [13]. Several kinetic parameters of the recombinant MGL derived from the pathogenic microorganisms C. tetani (causative agent of tetanus), C. spo-rogenes (causative agent of gas gangrene and enteritis), and P. gingivalis (causative agent of periodontitis) were determined in the present study; the data on the cytotoxic activity of the enzyme from these sources and from C. freundii were analyzed.
experimental
Bacterial cultivation and purification of the enzyme
Escherichia coli BL21 (DE3) cells containing the MGL genes from C. sporogenes, C. tetani, and P. gingivalis in the plasmid pET-28a [14] were cultured in an “inducing” medium [15] at 37°C under stirring (180 rpm) for 24 h. The cells were harvested by centrifugation and stored at -80°C. Cell disruption and the removal of nucleic acids were performed according to [16]. After the separation of nucleic acids, the preparations were transferred to a 50 mM potassium phosphate buffer, pH 8.0, containing 0.05 mM pyridoxal 5’-phosphate (PLP) using a “Centricon-30 ultrafiltration unit” (Amicon, USA). The polypeptide chains of the enzymes isolated from three sources contained the poly-histidine fragment MGSSHHHHHHSSGLVPRGSH at their N-termini. The preparations were purified using affinity chromatography on a column with a Ni2+IMAC -Sepharose sorbent (GE Healthcare, Sweden); a 10-500 mM imidazole gradient in a 50 mM potassium phosphate buffer, pH 8.0, containing 0.05 mM PLP was used for MGL elution. Fractions with the characteristic spectra of pyridoxal 5’-phosphate-dependent enzymes with X, at
420 nm were obtained at an imidazole concentration of 25-155 mM. Cultivation of the biomass of E. coli BL21 (DE3) cells containing a plasmid with the MGL gene from C. freundii and purification of the enzyme was carried out as per [17]. The concentrations of the purified preparations were determined using the coefficient A^278 = 0.8 [17]. The purity of the preparations was evaluated using electrophoresis under denaturing conditions according to the Laemmli method [18]. The bands in the electrophoregrams were identified by Coomassie R-250 staining [19] and Western blotting using the poly-histidine fragment HisProbe-HRP reagent (Thermo scientific, Rockford, IL, USA) [20].
The activity of the preparations in the y-elimination reaction was determined by the rate of formation of a-ketobutyric acid in the coupled reaction with D-2-hydroxy isocaproate dehydrogenase under the conditions described in [17]. One unit of enzyme activity was defined as the quantity of MGL catalyzing the formation of 1.0 ^M/min a-ketobutyrate at 30°C. The specific activities of the enzyme from C. tetani, C. sporogenes, P. gingivalis and C. freundii were 16.6, 12.8, 5.0, and 10.2 U/mg, respectively.
Cleavage of the His-tag fragment was performed in a reaction with thrombin. The reaction mixture (1 ml) containing 10 mg of the enzyme in a 50 mM potassium phosphate buffer, pH 8.0, 1 mM DTT, 0.05 mM PLP, and 100 units of thrombin were incubated for 24 h at 4°C. The product was then purified by gel filtration on a Superdex 200 column (GE Healthcare, Sweden) equilibrated with a 50-mM potassium phosphate buffer, pH 8.0, containing 1 mM DTT and 0.05 mM PLP. The homogeneity of the preparation was determined by electrophoresis under denaturing conditions.
Determination of the oligomeric composition of MGL from C. tetani, C. sporogenes, and P. gingivalis The molecular weights of the enzymes from C. teta-ni, C. sporogenes, and P. gingivalis were determined for the enzymes containing His-tag, and after the thrombin-facilitated cleavage of the tag, followed by gel filtration on a Superdex 200 10/300 GL column (GE Healthcare, Sweden). A 50 mM potassium phosphate buffer, pH 8.0, containing 0.05 mM PLP and 1 mM DTT was used for elution.
Determination of the steady-state kinetic parameters of the Y- and P-elimination reactions
The steady-state parameters of the y-and P-elimination reactions were determined by the formation rate of a-ketobutyric and pyruvic acids in coupled reactions with D-2-hydroxy isocaproate dehydrogenase and lactate dehydrogenase under the conditions described in [17] by varying the substrate concentrations in the reaction mixtures. The data were processed according to the Michaelis-Menten equation using the Enzfitter software program. The molecular weights of the enzyme subunits with allowance for His-tag (which were equal to 44.04, 44.36, an 44.08 kDa for MGL from C. tetani, C. sporogenes, P. gingivalis, respectively) were used in the calculations.
Evaluation of in vitro cytotoxicity
The cytotoxic activity of MGL of various origins was evaluated for the Fisher L5178y lymphadenosis cell line (a collection of tumor strains from the N.N. Blokhin Cancer Research Center), PC-3 and LnCap human
Substrate MGL from P. gingivalis MGL from C. tetani MGL from C. sporogenes MGL from C. freundii**
s-1 X , m’ mM k /K , cat m’ M-1s-1 kca^ s-1 K , m’ mM kcat m-V1" s-1 K , m’ mM kcat /Km, M-/ls-m kca^ s-1 K , m’ mM kcat /Km,1 m-vt '
L-Met 3.9 1.77 2.2X103 12 0.947 1.27 x 104 9.86 0.432 2.28x 104 6.2 0.7 8.85x 103
S-Et-L-Hcy 3.84 0.93 4.13X103 5.89 0.545 1.08X104 7.05 0.278 2.54x 104 6.78 0.54 1.26x 104
L-Met(SO) 5.05 12.22 4.13x 102 2.7 7.07 3.82 xl02 6.7 33.51 2.0xl02 2.52 6.21 4.06x 102
S-Et-L-Cys 8.05 2.17 3.71 x 103 7.08 0.72 9.83x 103 6.3 0.358 1.76xl04 5.03 0.17 2.96x 104
S-Bzl-L-Cys 5.8 1.47 3.94X103 8.5 0.766 1.11 x 104 10 0.348 2.87xl04 8.16 0.18 4.53x 104
* The mean squared error of the experiment in the determination of the kinetic parameters did not exceed 10%. ** Data from [16, 17].
Table 1. Kinetic parameters of MGL from various sources*
prostate cancer cell lines (ATCC, USA), the MCF7 human breast cancer cell line (ATCC , USA), K562 chronic erythroblastic human leukemia cell line (ATCC, USA), and the SKOV-3 human ovarian cancer cell line (a collection of tumor strains from the N.N. Blokhin Cancer Research Center). Cells were cultured at 37°C and 5% CO2 in the RPMI 1640 medium (PanEco, Russia) containing 10% of fetal bovine serum (HyClone Laboratories, UK), 2 mM L-glutamine, and 100 U/ml of penicillin and streptomycin (PanEco, Russia). The cells that reached the logarithmic growth phase were passed into 96-well flat bottom microplates (Costar, USA) - (4-6) x 104 cells per well - and pre-incubated for 24 h prior to the addition of the test enzymes under the abovementioned conditions. Light microscopy of the cells was carried out using an AxioVision 4 system (Carl Zeiss, Germany). Cell viability was determined using trypan blue dye exclusion staining (PanEco, Russia). Cell count was determined in the Goryaev chamber.
The MGL preparations in the RPMI 1640 medium in a wide range of progressively decreasing concentrations were added in the wells with the cell culture and co-incubated for 72 h. In addition to MGL, the culture medium contained 5 x 10-4 M PLP. The range of enzyme concentrations in the culture medium corresponded to 0.000001-6.2 U/ml. An equal volume of the RPMI 1640 medium with PLP was added in the control wells. The level of cell metabolism following the incubation period was determined using a standard MTT colorimetric assay [21]. The optical absorption of the dimethyl sulfoxide colored solutions was measured using a Multiskan MS plan-table photometer (Labsystems, Finland) at X = 540 nm. The viability of a cell culture after co-incubation with test substances was evaluated using the following formula: (N /N ) x 100%, where N is the optical absorbance in the test samples and Nc is
the optical absorbance in the control sample. The nonlinear regression method was used to calculate the inhibitory concentration of each enzyme in the medium; i.e., the concentration that caused a 50% reduction in the number of viable cells (IC).
Statistical data analysis
The data were processed using the SPSS 11.5 software package. The relationships between IC50 and Km were studied using the Pearson correlation analysis. The correlation coefficients were calculated for the grouped cytotoxicity data in various cell lines and for the ungrouped data. In the former case, the correlation analysis included the geometric mean of IC50 for various cell cultures. In the latter case, the cytotoxicity was individually assessed using each cell line; the data were pre-logarithmized for the symmetrization of the distribution law.
One-way ANOVA test was used to compare the cytotoxicity of the enzymes from C. freundii, C. sporogenes, and C. tetani. An analysis of the logarithmized data was conducted, since the dispersions of IC50 in the groups varied considerably. The mean values ± SD - arithmetic mean and standard deviation; geometric mean (antilog of the logarithmic means); pANOVA= 0.005 - statistical significance of the differences according to the data from the analysis of the variance in general were calculated. The statistical significance of the differences in the cytotoxic activity of various enzymes was evaluated using the Tukey method.
RESULTS AND DISCUSSION
Kinetic parameters of MGL from three pathogenic bacteria
We determined the steady-state kinetic parameters of MGL from three sources in the y-elimination reac-
40 kDa
12 3 4 5
86 kDa 43 kDa
Fig. 1. Electrophoresis
(a) and western blot
(b) of MGL from various sources.
1 - standard molecular weight markers,
2 - C. freundii MGL,
3 - P. gingivalisMGL,
4 - С. sporogenes MGL, 5 - C. tetani MGL
B
2
4
5
tion for three substrates: L-methionine, L-methio-nine sulfoxide, S-ethyl-L-homocysteine, and in the P-elimination reaction for two substrates - S-ethyl-L-cysteine and S-benzyl-L-cysteine. The data are presented in Table 1 in comparison with the parameters for the MGL from C. freundii.
In general, the kinetic parameters for the three enzymes and MGL isolated from C. freundii were comparable. The enzyme from C. sporogenes is characterized by the highest catalytic efficiency in comparison with other enzymes ^ /.^ value) in the reaction with the physiological substrate, and the enzyme from P. gin-givalis is characterized by the lowest catalytic activity. As mentioned above, antitumor activity was previously determined primarily for MGL from P. putida [22, 23]. The k t, K , k JK values for the y-elimination
L 7 J cat7 m7 cat' m *
reaction of L-methionine for MGL from this source are equal to 25.39 s-1, 0.92 mmol, and 2.76 x 104 M-1s-1, respectively [24]; i.e., the enzyme from C. sporogenes is characterized by a higher affinity to L-methionine than MGL from P. putida, but their catalytic efficiency is virtually identical.
Oligomeric structure of the recombinant proteins
It has previously been demonstrated that MGL from P. putida exists in solutions as a tetramer [25]. The X-ray diffraction analysis data for the recombinant MGL from C. freundii also indicated that the enzyme exists as a tetramer [26].
Two major bands have been revealed in the electro-phoregrams of denatured preparations from C. sporo-genes, C. tetani, and P. gingivalis. The first band with respect to the molecular weight corresponds to the MGL subunit; the second band is twice as large as the first one (Fig. 1A). Both of these bands interacted with the His-tag reagent (Fig. 1B). The bands corresponding to the dimeric form of MGL could form either during
the oxidation of the sulfhydryl groups of MGL under the conditions of Laemmli electrophoresis, or their formation could be attributed to the His-tag. In most cases, the presence of the His-tag at the N-or C-terminus of the recombinant proteins did not affect their structure and function [27]; however, data on the influence of the His-tag on the structure and function of proteins are available. Thus, it has been demonstrated [28] that the presence of the His-tag at the C-terminus restores the ability of the mutant form of the DNA binding protein n30 5 to form dimers, as opposed to the wild-type protein that is incapable of dimerization. The presence of the His-tag at the N-terminus of galactitol-l-phos-phate 5-dehydrogenase reduced the enzyme’s stability and resulted in aggregation of dimeric molecules [29].
It can be presumed that the presence of the MGSSH-HHHHHSSGLVPRGSH sequence at the N-termini of the polypeptide chains of MGL from C. sporogenes, C. tetani and P. gingivalis affects the oligomeric organization of the enzymes.
The molecular weights of the native MGL preparations from the three sources mentioned above and C. freundii were determined by gel filtration. It was established that all the enzymes, independent of their source, are characterized by a tetrameric form. Figure 2 shows the data on the gel filtration of MGL from C. sporogenes. It was demonstrated that the molecular weights of the preparations from C. sporogenes, C. teta-ni and P. gingivalis after cleavage of the His-tag by thrombin are all equal approximately to 170 kDa, which corresponds to the tetrameric form. It should be noted that the oligomeric form was identified in the MGL preparation from C. tetani (characterized by the physiological activity of MGL) with a molecular weight of approximately 258 kDa. No dimeric forms were detected in the electrophoregrams of any of the preparations (Fig. 3), which excludes the aforementioned possibility
Volume,ml
Fig. 2. Gel filtration of C. sporogenes MGL. The column was calibrated using standard markers: their molecular weights are shown in the figure
Fig. 3. Electrophoresis of C. sporogenes MGL. 1 - enzyme with His-tag fragment, 2 - enzyme after thrombin detachment of His-tag, 3 - standard molecular weight markers
2
3
that they form during the oxidation of the sulfhydryl groups of MGL under standard conditions of Laemmli electrophoresis. Therefore, the dimeric form of MGL is observed exclusively during the gel electrophoresis of denatured preparations from three sources containing a His-tag at the N-termini of polypeptide chains.
According to the X-ray diffraction analysis data, a tetrameric molecule of MGL from C. freundii consists of two catalytic dimers, each possessing two active sites formed by the residues of two subunits. The N-terminal domains of each subunit participate in the formation of a dimer, generating multiple hydrogen bonds with the residues of the C-terminal domain of the adjacent subunits and in the association of two catalytic dimers as they come into contact with the residues of the two C-terminal domains of the second catalytic dimer (Fig. 4) [26]. It is possible that the N-terminal His-tag present in the molecules of MGL from C. sporogenes, C. tetani and P. gingivalis forms additional bonds with residues of the C-terminal domain of the catalytic dimer and with the C-terminal residues of two subunits of the second catalytic dimer; thus, dimerization of the subunits can occur in denatured preparations.
The specific activity of the MGL preparations from C. sporogenes, C. tetani, and P. gingivalis determined after the cleavage of the His-tag by thrombin in the Y-elimination reaction of L-methionine turned out to be 1.5 times higher. The 50% increase in the specific activity of the preparations cannot be attributed exclusively to their minor additional purification after the treatment with thrombin. It is possible that the presence of a His-tag affects MGL activity.
In order to explain the variability in the catalytic efficiency of the enzymes and probable influence of the His-tag localized at the N-terminal regions of the polypeptide chains of the MGL from C. sporogenes, C. tetani, and P. gingivalis on enzyme activity, further investigations involving an X-ray diffraction analysis are required.
Cytotoxicity of methionine Y-lyase from
C. freundii, C. sporogenes and C. tetani The calculated IC50 values for MGL of various origins on a panel of cell cultures are presented in Table 2. PC-3 prostate cancer and K562 human chronic erythroblastic leukemia cell cultures were the ones most sensitive to the action of the enzymes; their IC50 values were
Table 2. IC50 of MGL for several tumor cell cultures
Cell culture IC50 of MGL, U/ml
С. freundii C. sporogenes C. tetani
K562 1.3 0.9 0.4
PC-3 0.1 0.4 -
LnCap > 2.9 > 2.9 >6.2
MCF7 0.5 0.04 3.2
L5178y 1.7 > 2.9 -
SCOV-3 - - 5.3
Fig. 4. Tetramer of C. freundii MGL. The subunits are marked using different colors, active sites are shown in pink, and the contact region between catalytic dimers is shown in yellow
0.1-0.4 and 0.4-1.3 U/ml, respectively. LnCap prostate cancer cells were the least sensitive: in the investigated concentration range, the IC50 value could not be determined for any of the enzymes. The sensitivity of K562 and MCF7 cells to the action of MGL is characterized by a significant variability.
The results obtained are indicative of the relatively high sensitivity of most of the cells that had been investigated to the action of MGL. Thus, the cytotoxicity of MGL is comparable to that of the other known enzymes, in particular, L-asparaginase from E. coli: with respect to the K562 and MCF7 cell cultures, the IC50 values for L-asparaginase from E. coli are equal to 0.8 and 10.9 U/ml, respectively [30]. The cytotoxicity level closest to that of MGL from P. putida was observed for the corresponding enzyme from C. sporogenes.
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CONCLUSIONS
The determination of the kinetic parameters and cytotoxic activity of MGL from three bacterial sources demonstrated that the enzyme from C. sporogenes shows promise and requires further research. It is characterized by a minimal Km value as compared to the other investigated enzymes and the highest cytotoxicity approaching that of MGL from P. putida.
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This work was supported by the Russian Foundation for Basic Research (grant № 11-04-12104-ofi-m-2012) and the grant of the President of the Russian Federation for state support of the leading scientific schools (№ 2046.2012.4).
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