Influence of metal ions on bioremediation activity of protocatechuate 3,4-dioxygenase from Stenotrophomonas maltophilia KB2
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- Guzik, U., Hupert-Kocurek, K., Sałek, K. et al. World J Microbiol Biotechnol (2013) 29: 267. doi:10.1007/s11274-012-1178-z
The aim of this paper was to describe the effect of various metal ions on the activity of protocatechuate 3,4-dioxygenase from Stenotrophomonas maltophilia KB2. We also compared activity of different dioxygenases isolated from this strain, in the presence of metal ions, after induction by various aromatic compounds. S. maltophilia KB2 degraded 13 mM 3,4-dihydroxybenzoate, 10 mM benzoic acid and 12 mM phenol within 24 h of incubation. In the presence of dihydroxybenzoate and benzoate, the activity of protocatechuate 3,4-dioxygenase and catechol 1,2-dioxygenase was observed. Although Fe3+, Cu2+, Zn2+, Co2+, Al3+, Cd2+, Ni2+ and Mn2+ ions caused 20–80 % inhibition of protocatechuate 3,4-dioxygenase activity, the above-mentioned metal ions (with the exception of Ni2+) inhibited catechol 1,2-dioxygenase to a lesser extent or even activate the enzyme. Retaining activity of at least one of three dioxygenases from strain KB2 in the presence of metal ions makes it an ideal bacterium for bioremediation of contaminated areas.
KeywordsAromatic compoundsDioxygenasesMetal ionsStenotrophomonas
Under aerobic conditions aromatic compounds are usually transformed to a few central intermediates such as catechols, protocatechuates, gentisates and (hydroxy)benzoquinols as a result of introduction of a new hydroxyl group at the ortho- or para-position to the existing one (Lillis et al. 2010; Guzik et al. 2011). Protocatechuic acid is a substrate for protocatechuate 3,4-dioxygenase [EC 18.104.22.168], enzyme catalyzing the intradiol cleavage of the aromatic ring, forming 3-carboxy-cis,cis-muconic acid (Contzen and Stolz 2000; Costas et al. 2004; Guzik et al. 2011). This enzyme belongs to a large class of the nonheme iron-containing dioxygenases and is composed of equimolar amounts of two α and β subunits (Ludwig et al. 1984; Buchan et al. 2000). The crystal structure of this enzyme shows that the high-spin iron(III) is bound to the active site in a distorted trigonal bipyramidal coordination geometry with two inequivalent tyrosine ligands, two histidines, and a hydroxide ion (Valley et al. 2005; Kurahashi et al. 2006; Mayilmurugan et al. 2010). The interaction of a substrate with Fe3+ causes the dissociation of both the axial tyrosine and the hydroxide resulting in a chelated “substrate-Fe3+” complex (Elgren et al. 1997; Vetting et al. 2000). This activates the substrate for an electrophilic attack by dioxygen, which leads to the formation of a peroxo bridge between iron and C4 of substrate (Pau et al. 2005; Borowski and Siegbahn 2006). Next, Criegee rearrangement (acyl migration to the peroxo oxygen) and O–O bond cleavage occurs, leading to the cyclic anhydride formation. The second atom of a molecular oxygen is retained at the Fe3+ as an oxide or hydroxide ion, where it functions as a nucleophile to hydrolyze the anhydride, yielding the ring open product (Vetting et al. 2000; Borowski and Siegbahn 2006). Due to the specific structure and mechanism of protocatechuate 3,4-dioxygenase-catalyzed reaction, the metal ions could influence the activity of this enzyme. During metalloenzymes catalysis, metal ions such as ferrum or calcium, are known to be the activators, since they induce conformational changes in the enzyme to stabilize the bound Fe2+ or to assist the orientation of catalysis site for a substrate binding (Ha et al. 2000). Gopal et al. (2005) suggested that the replacement of the iron in the active site with different metal ions caused the modulation of enzyme activity in accordance with the Irving-Williams order for bivalent metal ions. Several ions are known to be sulfhydryl groups` inhibitors and therefore change the conformation of a protein structure (Ha et al. 2000). In this paper we described the effect of various metal ions (Fe2+, Fe3+, Cu2+, Zn2+, Co2+, Al3+, Cd2+, Ni2+ and Mn2+) on the activity of protocatechuate 3,4-dioxygenase from Stenotrophomonas maltophilia KB2. As in strain KB2 induction of various types of dioxygenases was observed (Guzik et al. 2009), we compared the activity of these enzymes in the presence of different metal ions. Results of our studies seem to be very important for biodegradation processes since the metal ions present in the environment play an important role in bioremediation of aromatic compounds.
Materials and methods
Media and culture conditions for biodegradation of aromatic compounds
Stenotrophomonas maltophilia KB2 (VTT E-113197) is a gram-negative, aromatic compound-degrading bacterium isolated from the activated sludge of the sewage treatment plant in Bytom—Miechowice, Poland (Guzik et al. 2009; Wojcieszyńska et al. 2011b). 250 ml of the sterile MSM (Mineral Salt Medium) supplemented with 1 mM of the tested aromatic compound (phenol, protocatechuic acid, or benzoic acid) were inoculated with KB2 cells to the final optical density of about 0.1 in absorbance scale at λ = 600 nm (OD600), and incubated by shaking at 30 °C for 24 h. While growth of the cultures and complete degradation of the aromatic substrate was observed and OD600 of the culture was above 1.0, the proper volume of the culture was transferred to the new flask with sterile MSM to the final optical density of about 0.1 in absorbance scale at λ = 600 nm (OD600), the successive dose (2 mM and higher) of the aromatic substrate was added/introduced and the cultures were left for incubation for the next 24 h at 30 °C and 125 rpm. The residual aromatic compounds concentration in the culture filtrates was determined by the liquid chromatography.
Induction experiments were carried out in 1-l flasks, containing 500 ml of mineral salts medium and protocatechuic acid or benzoic acid at concentration of 6 and 10 mM, respectively. Protocatechuic acid and benzoic acid were used as the inducers of protocatechuate 3,4-dioxygenase and catechol 1,2-dioxygenase, respectively. Cells in the late exponential growth phase were used for enzymes isolation.
Determination of aromatic compounds concentration
In order to study the degradation of the aromatic compounds, samples were taken periodically from the culture medium and centrifuged (6,000×g, 15 min). Concentration of aromatic compounds in the culture supernatant was determined by HPLC (Merck HITACHI) equipped with a LiChromospher® RP-18 column (4 × 250 mm) and a DAD detector (Merck HITACHI). The wavelength for detection of substrates, composition of eluent and solvent as well as the flow rate were developed separately for each aromatic compound. The mobile phase, in phenol and benzoic acid determination was acetonitryl and water (50:50 v/v), in protocatechuic acid determination was methanol and 1 % acetic acid (25:75 v/v), at the flow rate of 1 ml·min−1. The detection wavelength was set at 285 nm for phenol and at 260 for benzoic and protocatechuic acids. Chemical compounds in the supernatant were identified and quantified by comparing HPLC retention times and UV-visible spectra with external standards.
Preparation of crude enzymatic extract
Cells were harvested in the late exponential growth phase by centrifugation at 5,000×g for 15 min at 4 °C. The cells were then washed with 50 mM phosphate buffer, pH 7.0, and resuspended in the same buffer. The obtained cell extracts were sonicated 6 times for 15 s and centrifuged at 9,500×g for 20 min at 4 °C. The supernatant was used as a crude extract for enzyme assays.
Activity of catechol 1,2-dioxygenase [EC 22.214.171.124] was measured spectrophotometrically by the formation of cis,cis-muconic acid at 260 nm (ε260 = 16,800 M−1 cm−1). The reaction mixture contained 20 μl of catechol (50 mM), 67 μl Na2EDTA (20 mM), 893 μl of phosphate buffer pH 7.4 (50 mM) and 20 μl of crude extracts in a total volume of 1 ml. Specific activity of protocatechuate 3,4-dioxygenase was assayed by measuring the consumption of oxygen. The reaction mixture contained 400 μl of protocatechuic acid (10 mM), 2,600 μl of phosphate buffer pH 7.2 (50 mM) and 1,000 μl of crude extract in a total volume of 4 ml according to Hou et al. (1976). Protein concentrations of the crude extracts were determined by the Bradford method (Bradford 1976).
Effect of various metal ions on enzyme’s activity
The effects of metal ions on enzymes` activity were investigated using FeSO4, FeCl3, CuSO4, ZnCl2, CoCl2, AlCl3, CdSO4, NiCl2, and MnSO4. Protocatechuate 3,4-dioxygenase was preincubated in the phosphate buffer (50 mM, pH 7.2) containing: Fe2+, Fe3+, Cu2+, Zn2+, Co2+, Al3+, Cd2+, Ni2+, Mn2+ at a final concentration of 1–3 mM for 3 min at 30 °C. Effect of the metal ions on the activity of catechol 1,2-dioxygenase was studied by incubating it in the presence of above mentioned ions at concentration of 3 mM. After incubation, a residual enzymatic activity was measured as described above.
Results and discussion
Degradation of aromatic compounds by S. maltophilia KB2
Strain KB2 degraded 10 mM BA during 24 h (Fig. 1b) while Streptomyces setonii was capable of degrading only 5 mM of this substrate (An et al. 2000). Moreover, high concentrations of benzoate inhibited growth of Pseudomonas putida (Loh and Chua 2002). In contrast to the results obtained by Loh and Chua (2002), an inhibitory effect of benzoate was not observed by Muthukumar et al. (2009), during degradation of 25 mM benzoic acid by Micrococcus sp.
In our work we demonstrated that strain KB2 was also able to utilize 12 mM phenol during 24 h of incubation (Fig. 1c). Similar results were obtained by Shumakova et al. (2009) and Essam et al. (2010), who showed the ability of Rhodococcus opacus strain 1G and Alcaligenes strain TW1 to degrade 10 mM and 12 mM phenol, respectively. Degradation tests for the Acinetobacter strain ATTC11171 made by Adav et al. (2007) showed that this strain fully degraded 5 mM phenol, while at phenol concentrations higher than 5 mM, an inhibitory effect was observed. Phenol at low concentrations (1 and 2 mM) was degraded completely by Ochrobactrum AS1 and Fusarium flocciferum (El-Sayed et al. 2003; Mendonça et al. 2004). Our results show that strain KB2 exhibits ability to degrade a wide range of aromatic compounds at relatively high concentrations what makes it exceedingly attractive for industrial applications especially in bioremediation and wastewater treatment.
Influence of metal ions on protocatechuate 3,4-dioxygenase activity
As it is generally known interactions between metal ions and residues in proteins are important for the protein’s stability, however metals are also known to be powerful inhibitors of the enzyme’s activity. Due to simultaneous contamination of industrial wastes by aromatic compounds and metals (Wu et al. 2008; Deeb and Altalhi 2009), there is an increasing interest in identification of enzymes that degrade aromatic structure and are resistant, among other factors, to the metal ions. In our study we examined influence of various metal ions on protocatechuate 3,4-dioxygenase, the non-heme iron—containing enzyme that catalyzes the ortho cleavage of the aromatic ring between the vicinal hydroxyls to form β-carboxy-cis,cis-muconic acid (Luo et al. 2008).
Relative activity of protocatechuate 3,4-dioxygenase from strain KB2 in the presence of various metal ions (the plus/minus values represent standard deviation)
Relative activity, %
100 ± 0.00
43.00 ± 4.67
119.93 ± 2.32
128.92 ± 3.11
41.65 ± 5.72
34.62 ± 1.49
22.76 ± 2.11
41.81 ± 4.07
27.36 ± 2.60
29.64 ± 0.63
94.27 ± 7.21
71.79 ± 5.17
50.95 ± 2.76
74.34 ± 19.14
70.58 ± 8.45
51.55 ± 4.69
89.99 ± 5.43
68.39 ± 3.21
33.50 ± 2.14
69.33 ± 4.01
63.85 ± 2.14
60.20 ± 12.65
78.65 ± 3.02
88.34 ± 2.29
83.34 ± 0.31
108.06 ± 8.19
98.55 ± 5.08
80.92 ± 5.43
Intradiol dioxygenases contain a trivalent metal ion that is coordinated by four strictly conserved amino acid residues and one solvent molecule (Valley et al. 2005; Matera et al. 2008). A typical characteristic of most ortho-fission dioxygenases described so far is the increase of its activity by the addition of Fe3+ (Yeom and Yoo 1997; Iwagami et al. 2000). Iwagami et al. (2000) and Wu et al. (2008) stated that in metal ion catalysis, metals act as activators which induce conformational changes of the enzyme to stabilize it or support substrate binding by providing correct orientation of the catalytic site. However, we did not observe this effect. As shown in Table 1, the protocatechuate 3,4-dioxygenase from strain KB2 was inhibited by the addition of Fe3+. Similar effect was observed by Yeom and Yoo (1997) for Alcaligenes xylosoxidans catechol 1,2-dioxygenase. Transition metals such as Fe3+ rapidly react with sulfhydryl groups of cysteine residues which in turn affect tertiary structure of the enzyme. Partial loss of protocatechuate 3,4-dioxygenase’s activity in the presence of ferric ions might be caused by binding of Fe3+ ion to a site other than the active site of enzyme resulting in conformational changes in protein structure. To our surprise, the Fe2+ ions activated the examined enzyme. Similar effect was also observed by Yeom and Yoo (1997) in studies on the influence of metal ions on catechol 1,2-dioxygenases from A. xylosoxidans Y234. The influence of Fe2+ on protocatechuate 3,4-dioxygenase remains unsolved and needs further investigations.
Effects of various metal ions on dioxygenases’ activity
Relative activity of dioxygenases from strain KB2 in the presence of various metal ions (the plus/minus values represent standard deviation)
Ion (3 mM)
Relative activity, %
Catechol 2,3-dioxygenase (Guzik et al. 2010)
100.00 ± 0.00
100.00 ± 0.00
128.92 ± 3.11
142.42 ± 3.21
22.76 ± 2.11
58.18 ± 8.33
29.64 ± 0.63
105.68 ± 17.68
50.95 ± 2.76
145.07 ± 2.68
51.55 ± 4.69
162.12 ± 18.21
33.50 ± 2.14
84.47 ± 4.82
60.20 ± 12.65
271.21 ± 26.78
83.34 ± 0.31
0.00 ± 0.00
80.92 ± 5.43
72.73 ± 2.14
The complete inhibition of catechol 1,2-dioxygenase activity was observed in the presence of Ni2+. As it is known this cation tends to bind to cysteine or histidine residues in the proteins (Nies 1999). Since histidines are the key residues forming the active site of the intradiol dioxygenases, the loss of catechol 1,2-dioxygenase activity was probably connected with interaction of Ni2+ with this amino acid. In spite of lower or even no activity of both: catechol 1,2- and 2,3-dioxygenase in the presence of nickel ions, strain KB2 could be still used in degradation of aromatic compound under these conditions due to the fact that protocatechuate 3,4-dioxygenase from this strain was minimally affected by Ni2+ (Table 2).
In summary, degradation of the selected aromatic compounds by S. maltophilia KB2 is catalyzed by one of three types of dioxygenases induced in this strain depending on the substrate used. These enzymes showed different sensitivity to the metal ions. Catechol 1,2- and 2,3-dioxygenase from this strain were strongly inhibited by Ni2+ ions while under the same conditions, protocatechutae 3,4-dioxygenase retained 80 % of its initial activity. In contrast Cu2+ ions inhibited protocatechuate 3,4-dioxygenase and catechol 2,3-dioxygenase while any negative effect of these ions on catechol 1,2-dioxygenase was observed. Induction of three types of dioxygenases in S. maltophilia KB2 ensure a degradation of aromatics which are present in the environment simultaneously contaminated with various metal ions.
This work was supported by Polish Ministry of Science and Higher Education (IP2010012170). Małgorzata Sitnik is acknowledged for an excellent technical assistance.
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