Influence of kaolinite on chiral hydrolysis of methyl dichlorprop enantiomers

Influence of kaolinite on chiral hydrolysis of methyl dichlorprop enantiomers first-author corresp ‡Corresponding Author ‡Corresponding Author †E-mail:environment@zju.edu.cn †E-mail:environment@zju.edu.cn environment@zju.edu.cn Institute of Environmental Science, Zhejiang University, Hangzhou 310029, China Institute of Environmental Science, Zhejiang University, Hangzhou 310029, China The effect of kaolinite on the enzymatic chiral hydrolysis of methyl dichlorprop enantiomers ((R,S)-methyl-2-(2,4-dichlorophenoxy) propanoic acid, 2,4-DPM) was investigated using chiral gas chromatography. Compared with the control without kaolinite, the enantiomeric ratio (ER) increased from 1.35 to 8.33 and the residual ratio of 2,4-DPM decreased from 60.89% to 41.55% in the presence of kaolinite. Kaolinite likely had emotion influence on lipase activity and its enantioselectivity. Moreover, the amount of kaolinite added was also found to be a sensitive factor affecting the enantioselective hydrolysis of 2,4-DPM. Fourier transform infrared (FTIR) spectroscopy studies of the interaction of lipase with kaolinite provided insight into the molecular structure of the complex and offered explanation of the effects of kaolinite on enzymatic hydrolysis of 2,4-DPM. Spectra showed that the effect of kaolinite on the hydrolysis of 2,4-DPM was affected by adsorption of lipase on kaolinite and changes of adsorbed lipase conformation, which led to the modified enantioselectivity. Enantioselectivity Kaolinite Chiral gas chromatography Methyl dichlorprop Lipase INTRODUCTION 1 Lipase (EC 3.1.1.3) is an important hydrolysis enzyme (Jaeger et al., 1994 1994 ) excreted to the environment by plant roots and microorganisms. Many pollutants such as organophosphorus pesticides and synthetic polyesters and polyamides can be degraded by lipase (Monroy-Noyola et al., 1999 1999 ; Marten et al., 2003 2003 ). In soil, enzymatic reactions occur in a heterogeneous rather than homogeneous environment (Huang et al., 1998 1998 ). Catalytic function of lipase, an extracelluar enzyme, is associated with soil clays. Consequently, properties and kinetic behavior such as enantioselectivity and activity of enzyme-clay complexes will differ from those of the free enzyme. The modulation of the activity of lipase via immobilization on different phyllosilicates was reported (de Fuentes et al., 2001 2001 ). To the author’s best knowledge, the influence of clays on lipase enantioselectivity had not been investigated before. In the present study, dichlorprop methyl ester ((R,S)-2,4-DPM), a typical chiral contamination, was enzymatically hydrolyzed in aqueous systems by lipase. Kaolinite was applied to the enzymatic reaction system, and its influence on the lipase enantioselectivity and performance was studied with chiral gas chromatography (GC) and Fourier transform infrared (FTIR). MATERIALS AND METHODS 1 Chemicals 2 Kaolinite was purchased from Shanghai Fengxian Fengcheng Agent Factory, China. Lipase was obtained from Shenzhen Leveking Biology Engineering Co., China. Racemate and optically pure enantiomer of methyl dichlorprop (2,4-DPM) was synthesized and confirmed by NMR and mass spectroscopy. Stock solution of (R,S)-2,4-DPM was prepared in methanol at 1.0 mg/ml and stored at 4 °C before use. Working standard solutions were prepared daily by diluting the stock solutions with phosphate buffer. Other solvents and chemicals used in this study were analytical-reagent grade. Enzyme-catalyzed hydrolysis reactions 2 The effect of kaolinite on lipase-catalyzed hydrolysis of 2,4-DPM was carried out in the dark. Ten ml of 0.05 mol/L phosphate sodium buffer (pH 7.00) was placed in 50 ml flask, and then 2.5 mg lipase dry powder and 0.1 ml 2,4-DPM stock solution (1.0 mg/ml) were added into the flask. Kaolinite was added to the system at 20 mg per flask, and the mixture was incubated at 25 °C on a rotary shaker at 100 r/min for 8 h. Aliquots (0.2 ml) of the reaction mixture were withdrawn and extracted with 2 ml of n -hexane, followed by drying over anhydrous Na 2 SO 4 . The samples were analyzed using chiral GC. Each treatment was sampled in triplicates, and the enzyme-free samples were included as controls for analytical background of enzyme activity. Influence of kaolinite addition rate and 2,4-DPM concentration 2 Kaolinite at rates of 0, 5, 10, 20, 40, 80, or 160 mg per flask was added to 10 ml phosphate buffer (pH 7.00) in 50 ml flasks, followed by addition of 2.5 mg lipase dry powder and 0.1 ml 2,4-DPM stock solution. The mixture was incubated for 8 h under the same conditions as described above. Triplicate samples were extracted with n -hexane and analyzed by GC. In the presence of 20 mg kaolinite, 2,4-DPM stock solutions in the amount of 20, 30, 40, 60, 100, or 160 µl was fortified into 10 ml phosphate buffer in 50 ml flasks. The initial concentration of 2,4-DPM was 2, 3, 4, 6, 10, 16 µg/L, respectively. The other conditions were the same as given above. GC analytical procedure 2 Chiral GC analyses were carried out using an Agilent 6890N GC with micro-cell electron capture detector (µ-ECD) equipped with a 30 m×0.25 mm×0.25 µm BGB-176 chiral column (BGB Analytik, Adliswil, Switzerland). The inlet temperature was 200 °C, and 1 µl sample was introduced in the splitless mode. The column was held at 140 °C and the carrier gas (N 2 ) flow rate was 1.2 ml/min. The detector temperature was 300 °C, and the detector makeup gas was N 2 (60 ml/min). Chiral synthesized (R)-2,4-DPM and (S)-2,4-DPM (US 4622415) were used as the sole criterion for identifying peaks in GC-ECD chromatograms under the conditions used, gave peaks with retention times of 32.6 min and 35.0 min, respectively. The enantiomeric ratio (ER) was expressed as the peak area of R-isomer divided by that of S-isomer. FTIR measurements 2 The complex of lipase and kaolinite was prepared according to the procedure described previously with a little modification (de Fuentes et al., 2001 2001 ). Fifty mg lipase dry powder and 250 mg kaolinite were added to a flask containing 50 ml phosphate buffer (pH 7.00), and stirred at 4 °C for 24 h. Filtered samples were then washed twice with distilled water and freeze-dried. The samples of the solid lipase and kaolinite complex, the mechanical mixture of 1/10 ( w / w ) lipase with kaolinite and lipase dry powder were mixed with KBr and examined on a Shimadzu FTIR-8900. RESULTS AND DISCUSSION 1 Effect of kaolinite on the lipase performance 2 Our investigation on the influence of kaolinite on lipase performance in hydrolysis of 2,4-DPM (Table 1 1 ) showed that kaolinite could enhance the enzymatic hydrolysis rate of 2,4-DPM and that the residual ratio of 2,4-DPM decreased from 60.89% to 41.55%. Our results agreed with the previous reports (de Fuentes et al., 2001 2001 ) that kaolinite added could enhance the lipase activity. Additive amount (mg) Reaction time (h) ER Residue ratio (%) Control 0 8 1.04 100 No additive 0 8 1.35 60.89 Kaolinite 20 8 8.33 41.55 Clay served as an absorbent yielding a stable substrate with a large interfacial area. This may contribute to the improvement of lipase activity, as shown in Table 1 1 . The enhancement effect also might be attributed to the hydrogen-bonding and hydrophobic interaction between the lipase with clay, which could induce an unfolding and open-structure of the enzyme (Fernandez-Lorente et al., 2001 2001 ; Palomo et al., 2002 2002 ). Effect of kaolinite on the enantioselective ratio of 2,4-DPM enzymatic hydrolysis 2 Fig. 1 1 shows that the lipase displayed only low enantioselectively ( ER =1.35), and this provides us with a sensitive system to detect small changes in enantioselectivity. The effect of kaolinite on the lipase enantioselectivity is presented in Table 1 1 showing that in the presence of 20 mg kaolinite, the enantioselectivity of lipase was significantly increased, resulting in the increase of the ER value from 1.35 to 8.33 (Fig. 1 1 ). The results suggested a crucial role of kaolinite in the enhancement of enantioselectivity of lipase. In the presence of kaolinite, the S-enantiomer became overwhelmingly the faster reacting enantiomer. From the enantioselective ratio (ER value), it was apparent that the enhancement of enantioselectivity was the consequence of a differential activator phenomenon. Kaolinite acted as enantioselective activator of 2,4-DPM enzymatic hydrolysis. Effect of addition rate of kaolinite on enantioselectivity of enzymatic reaction 2 In the process of enzymatic reaction with kaolinite as additive, its addition rate is another important parameter worthy of careful measurement since it may also have influence on enzyme activity and enantioselectivity. The enantioselectivity seems to be the most crucial factor for enzymatic hydrolysis of chiral pesticides in the environment. The enantioselectivity of the enzymatic reaction depended on the amount of kaolinite added (Fig. 2 2 ). Within the range of 0~20 mg kaolinite, the ER value of the enzymatic reaction rapidly increased from 1.35 to 8.33. Above 20 mg, the ER value increased more slowly. When the amount of kaolinite added was small, lipase molecules were not completely adsorbed on kaolinite, so the ER value increased rapidly along with the amount of kaolinite. While the amount of kaolinite was over 20 mg, most of the lipase molecules were adsorbed on kaolinite, and the ER value increased more slowly with the amount of kaolinite. These results show that adsorption of lipase on clay is important in lipase enantioselectivity. Effect of 2,4-DPM concentration on the lipase enantioselectivity 2 Fig. 3 3 shows that the ER value was almost a constant ( ER =1.35) in enzymatic system in the range of the given pesticide concentrations. With 20 mg kaolinite were added to the enzymatic system, the adsorption of 2,4-DPM and lipase on kaolinite might occur simultaneously. When the pesticide concentration was very low, the adsorption of lipase on clay was more important. The ER value appreciably increased along with the pesticide concentration. As the pesticide concentration increased gradually, pesticide molecules occupied the adsorptive sites of clay, and the adsorbed lipase became less and the ER value decreased. FTIR spectra 2 In order to further understand the effects of kaolinite on hydrolysis, we investigated the IR spectra of the complex of lipase and kaolinite by using Fourier transform infrared (FTIR) spectroscopy. As shown in Fig. 4 4 , the characteristic spectrum corresponded to kaolinite covered in 450~4000 cm −1 . However, most of the characteristic spectrum corresponding to lipase was masked by the enormous amount of kaolinite. Thus, the carbonyl stretching band of the lipase carbonyl group, centered at 1651.0 cm −1 , was analyzed for the spectra. Fig. 4 4 shows that there was no difference between lipase with the 1/10 ( w / w ) mixture of lipase and kaolinite at 1651.0 cm −1 . This indicates that lipase did not interact with kaolinite in the mechanical mixture. a: Lipase; b: Lipase-kaolinite complex; c: 1/10 ( w / w ) mixed lipase with kaolinite On the other hand, Fig. 4 4 shows that the maximum of the carbonyl band (1651.0 cm −1 ) in lipase shifted to higher frequencies (1654.8 cm −1 ) compared with the lipase-kaolinite complex. This may be attributed to the disruption of the strong hydrogen bonds in the lipase and their replacement by a weak association. It shows that kaolinite induced an unfolding and open-structure of lipase (Fernandez-Lorente et al., 2001 2001 ), which may contribute to the increased lipase activity by kaolinite. CONCLUSION 1 Investigation of the effect of kaolinite on the lipase-catalyzed chiral hydrolytic degradation of dichlorprop methyl enantiomers in this work showed that kaolinite had potential for greatly enhancing the reaction rate and the enantioselectivity in the lipase-catalyzed reaction. In the presence of 20 mg kaolinite, the enantiomeric ratio (ER) increased from 1.35 to 8.33 and the residual ratio of 2,4-DPM decreased from 60.89% to 41.55%. Moreover, the amount of kaolinite added was found to be a sensitive factor affecting the enantioselective hydrolysis of 2,4-DPM. Within the range of 0~20 mg kaolinite, the ER value of the enzymatic reaction rapidly increased from 1.35 to 8.33, while the increase was slower when kaolinite was >20 mg. In the test system, clay seemed to play a triple role. First, it served as an absorbent to give a stable, large interfacial area substrate for the enzyme. Second, the nature of clay enabled it to be an activator of the lipase. Finally, an important role of clay was its ability to enhance the enantioselectivity. FTIR spectroscopy analysis of the complex of lipase and kaolinite provided further insight into the molecular structure of the complex and explanation for the effect of kaolinite on enzymatic hydrolysis of chiral 2,4-DPM. Data showed that a complex had formed between lipase and kaolinite and that kaolinite may have induced an unfolding and open-structure of lipase, which led to the increased lipase performance. References IE de Fuentes , CA Viseras , D Ubiali , M Terreni , AR Alcantara . Different phyllosilicates as supports for lipase immobilization . Journal of Molecular Catalysis B: Enzymatic , 2001 . 11 ( 4-6 ): 657 - 663 . . Different phyllosilicates as supports for lipase immobilization G Fernandez-Lorente , M Terreni , C Mateo , A Bastida , R Fernandez-Lafuente , P Dalmases , J Huguet , JM Guisan . Modulation of lipase properties in macro-aqueous systems by controlled enzyme immobilization: enantioselective hydrolysis of a chiral ester by immobilized pseudomonas lipase . Enzyme and Microbial Technology , 2001 . 28 389 - 396 . . Modulation of lipase properties in macro-aqueous systems by controlled enzyme immobilization: enantioselective hydrolysis of a chiral ester by immobilized pseudomonas lipase PM Huang , N Senesi , J Buffle . Structure and Surface Reactions of Soil Particles , 1998 . : New York Wiley , 449 - 479 . . Structure and Surface Reactions of Soil Particles KE Jaeger , S Ransac , BW Dijkstra , C Colson , M van Heuvel , O Misset . Bacterial lipases . FEMS Microbiology Reviews , 1994 . 15 29 - 63 . . Bacterial lipases E Marten , RJ Muller , WD Deckwer . Studies on the enzymatic hydrolysis of polyesters: I. Low molecular mass model esters and aliphatic polyesters . Polymer Degradation and Stability , 2003 . 80 485 - 501 . . Studies on the enzymatic hydrolysis of polyesters: I. Low molecular mass model esters and aliphatic polyesters A Monroy-Noyola , MA Sogorb , E Vilanova . Enzyme concentration as an important factor in the in vitro testing of the stereospecificity of the enzymatic hydrolysis of organophosphorus compounds . Toxicology in Vitro , 1999 . 13 689 - 692 . . Enzyme concentration as an important factor in the in vitro testing of the stereospecificity of the enzymatic hydrolysis of organophosphorus compounds JM Palomo , G Fernandez-Lorente , C Mateo , C Ortiz , R Fernandez-Lafuente , JM Guisan . Modulation of the enantioselectivity of lipases via controlled immobilization and medium engineering: hydrolytic resolution of mandelic acid esters . Enzyme and Microbial Technology , 2002 . 31 775 - 783 . . Modulation of the enantioselectivity of lipases via controlled immobilization and medium engineering: hydrolytic resolution of mandelic acid esters 10.1631/jzus.2005.B1028 Project supported by the National Natural Science Foundation of China (No. 30270767) and the National Nature Science Foundation of China for the Distinguished Young Scholars Program (No. 20225721) 2005-04-28 2005-07-13 2005-09-28 2022-01-05 Copyright © 2005, Journal of Zhejiang University Science 2005 Journal of Zhejiang University-SCIENCE B (Biomedicine and Biotechnology) 10 6B