Bioremediation of fluorophenols by glycosylation with immobilized marine microalga amphidinium crassum.

Fluorophenols are used as agrochemicals and released into environment as pollutants. Cultured marine microalga Amphidinium crassum (Gymnodinium) glucosylated 2-fluorophenol (1), 3-fluorophenol (2), and 4-fluorophenol (3) to the corresponding β-D-glucosides, ie, 2-fluorophenyl β-D-glucoside (4, 60 μg/g cells), 3-fluorophenyl β-D-glucoside (5, 20 μg/g cells), and 4-fluorophenyl β-D-glucoside (6, 40 μg/g cells). On the other hand, 2-, 3-, and 4-fluorophenols were efficiently converted by immobilized A. crassum in sodium alginate gel to give their β-D-glucosides in higher yields (4: 140 μg/g cells; 5: 60 μg/g cells; 6: 100 μg/g cells). In repetitive batch use, the immobilized cells of A. crassum maintained the potential for the glucosylation of the substrate fluorophenol after 5 times of usage.

Introduction

Fluorophenolic compounds are used to agrochemicals and pharmaceuticals, and cause serious environmental contamination.1 Number of fluorine-containing agricultural chemicals has grown from 4% to approximately 9% of all agrochemicals and has increased in number faster than non-fluorinated agrochemicals over the past 15 years.1 These compounds are primarily used as herbicides (48%), insecticides (23%), and fungicides (18%), and their residues are released as pollutants into rivers and seas. Many studies on biological degradation of halophenols by microorganisms have been reported.1–9 However, halophenols containing stable carbon-halogen bond in their structures have been described to be much more resistant to microbial degradation than unsubstituted analogs.1

Cell cultures are ideal systems for studying biotransformations such as glycosylation reactions.10 Some freshwater microalga can convert exogenous toxic compounds into glycosides.11 From the viewpoint of seawater pollution control, glycosylation of halophenols by marine microalga is of importance. This study focused on the metabolism of mono-fluorophenols by cultured and immobilized marine microalga of Amphidinium crassum.

Material and Methods

General

Substrates, 2-, 3-, and 4-fluorophenols, were purchased from Aldrich Chemical Co. The 1H and 13C NMR, H-H COSY, C-H COSY, and HMBC spectra were recorded using a Varian XL-400 spectrometer in CD3OD solution. Chemical shifts were expressed in δ (ppm) referring to tetramethylsilane. FABMS spectra were measured using a JEOL MStation JMS-700 spectrometer. A. crassum cells (5 g) were cultivated in a synthetic seawater (500 ml) for 2 weeks at 20 °C with constant aeration by air (1l/min) in 1 l flasks under illumination (1000lx). Constituents of synthetic seawater are summarized in Table 1.

Table 1.

The constituents of synthetic seawater.

Constituentsa	Conc. (g/l)	Constituentsa	Conc. (g/l)
NaCl	20.7	AlCl3 ·6H2O	8 × 10−6
MnCl2 ·4H2O	1 × 10−6	FeCl3 ·6H2O	5 × 10−6
MgCl2 ·6H2O	9.5	Na2WO4 ·2H2O	2 × 10−7
CaCl2 ·6H2O	1.3	(NH4)6MO7O24	2 × 10−5
Na2SO4	3.5	Na2SiO3	5 × 10−2
KCl	0.6	NaNO3	0.2
NaHCO3	0.2	Na2HO4	1 × 10−2
KBr	9 × 10−2	EDTA-2 Na	9 × 10−4
Na2B4O7 ·10H2O	3 × 10−2	Vitamin B12	2 × 10−6
SrCl2	1 × 10−2	Thiamine·Hcl	8 × 10−5
NaF	3 × 10−3	Biotin	1 × 10−6
LiCl	1 × 10−3	EDTA-Fe	3 × 10−3
KI	7 × 10−5	H2NC(CH3OH)3	5 × 10−3
COCl2 ·6H2O	2 × 10−7

Note:

Constituents are dissolved in distilled water.

Biotransformation of fluorophenols by A. crassum

Cultured A. crassum cells were harvested by centrifugation at 1000 g for 15 min and washed twice by adding 100 ml of synthetic seawater followed by centrifugation (1000 g for 15 min). To the 500 ml flask containing 9 g of cultured A. crassum cells and 300 ml of a synthetic seawater was added 0.2 mmol of substrate. Cultures were incubated at 20 °C with aerobic shaking for five days under illumination (1000lx). After the incubation period, the cells and synthetic seawater were separated by centrifugation at 1000 g for 15 min. Synthetic seawater was extracted with ethylacetate and then n-butanol. Cells were extracted (three times) by homogenization with methanol, and the methanol fraction was concentrated and partitioned between water and ethylacetate. Ethylacetate fractions were analyzed by HPLC, combined, and concentrated. This water fraction and n-butanol fraction extracted from medium were analyzed by HPLC, combined, evaporated, and re-dissolved in water. This water fraction was applied to a Diaion HP-20 column and the column was washed with water followed by elution with methanol. Methano l eluate was subjected to preparative HPLC to give glycosylation products. Yield of the products was determined on the basis of the peak area from HPLC. Product yields in μg/g cells (dry weight) was calculated based on the starting cell concentration. Control free suspended cells, which had not been treated with substrates, were subjected to the same extraction procedures and HPLC analyses as planktonic biotransformation experiments, and no products or substrates were detected in the cells and in the medium despite careful HPLC analyses.

Spectral data of products are as follows.

2-Fluorophenyl β-D-glucoside: FAB-MS m/z: 297 [M+Na]+; 1H NMR (400 MHz, CD3OD, δ in ppm): 3.41–3.89 (6H, m, H-2′-H-6′), 4.97 (1H, d, J = 8.0 Hz, H-1′), 6.96–7.01 (1H, m, H-4), 7.04–7.09 (2H, m, H-3, H-6), 7.25–7.30 (1H, dd, J = 1.6 Hz, J = 8.4 Hz, H-5); 13C NMR (100 MHz, CD3OD, δ in ppm): 62.3 (C-6′), 71.1 (C-4′), 74.6 (C-2′), 77.8 (C-3′), 78.0 (C-5′), 102.5 (C-1′), 117.0 (1C, d, J F-3C = 18.9 Hz, C-3), 119.1 (C-6), 123.8 (1C, d, J F-4C = 6.6 Hz, C-4), 125.4 (1C, d, J F-5C = 4.2 Hz, C-5), 146.3 (1C, d, J F-1C = 10.8 Hz, C-1), 153.9 (1C, d, J F-2C = 244.2 Hz, C-2).

3-Fluorophenyl β-D-glucoside; FAB-MS m/z: 297 [M+Na]+; 1H NMR (400 MHz, CD3OD, δ in ppm): 3.39–3.90 (6H, m, H-2′-H-6′), 4.92 (1H, d, J = 7.2 Hz, H-1′), 6.74 (1H, m, H-4), 6.85 (1H, m, H-2), 6.90 (1H, dd, J = 2.2 Hz, J = 8.0 Hz, H-6), 7.27 (1H, m, H-5); 13C NMR (100 MHz, CD3OD, δ in ppm): 62.3 (C-6′), 71.2 (C-4′), 74.7 (C-2′), 77.7 (C-3′), 78.0 (C-5′), 102.1 (C-1′), 105.2 (1C, d, J F-4C = 25.5 Hz, C-4), 109.7 (1C, d J F-2C = 20.6 Hz, C-2), 113.4 (1C, d, J F-6C = 2.4 Hz, C-6), 131.3 (1C, d, J F-5C = 9.9 Hz, C-5), 160.1 (1C, d, J F-1C = 10.5 Hz, C-1), 164.5 (1C, d, J F-3C = 241.7 Hz, C-3).

4-Fluorophenyl β-D-glucoside; FAB-MS m/z: 297 [M + Na]+; 1H NMR (400 MHz, CD3OD, δ in ppm): 3.35–3.90 (6H, m, H-2′-H-6′), 4.85 (1H, d, J = 7.2 Hz, H-1′), 6.95–7.01 (2H, m, H-3, H-5), 7.08–7.12 (2H, m, H-2, H-6); 13C NMR (100 MHz, CD3OD, δ in ppm): 62.4 (C-6′), 71.2 (C-4′), 74.7 (C-2′), 77.8 (C-3′), 78.0 (C-5′), 102.9 (C-1′), 116.4 (2C, d, J F-3, 5C = 23.1 Hz, C-3, C-5), 119.3 (2C, d, J F-2, 6C = 8.3 Hz, C-2, C-6), 155.2 (1C, d, J F-1C = 2.5 Hz, C-1), 159.4 (1C, d, J F-4C = 237.6 Hz, C-4).

Biotransformation of fluorophenols by immobilized A. crassum cells in sodium alginate gel

Sodium alginate (2%) was suspended in water (50 ml), which was autoclaved at 120 °C for 30 min. Cultured A. crassum cells (9 g) were added to this solution and the mixture was stirred for 2h until it became homogeneous. Suspension was added drop-wise from a dropping funnel with a glass tube into a 5% CaCl2 solution (1l) with stirring to form pieces of spherical sodium alginate gel with 5 mm diameter immediately. After washing with a synthetic seawater, immobilized A. crassum cells were used for biotransformation experiments.

To the immobilized A. crassum cells which included 9 g of A. crassum cells with 250 ml of the synthetic seawater in a 500 ml flask was added 0.2 mmol of substrate. Effect of sodium alginate concentration on the glycosylation of 2-fluorophenol (1) was examined by using the cells immobilized with sodium alginate at final concentrations of 1, 2, 3, 4, and 5%. Flask was incubated at 20 °C with aerobic shaking for five days under illumination (1000lx). Isolation of products was carried out by the similar procedures to planktonic biotransformation experiment described above.

Results and Discussion

Biotransformation product was isolated from the cultured cells of A. crassum, which had been treated with 2-fluorophenol (1) for 48 h. Potentially glucosylated product (4) was obtained, and no additional conversion products were observed in spite of the careful HPLC analyses. Chemical structure of the product was determined on the basis of their FABMS, 1H and 13C NMR, H-H COSY, C-H COSY, and HMBC spectra as 2-fluorophenyl β-D-glucoside (60 μg/g cells) (Fig. 1). Other microalga, ie, Chattonella sp. and Heterosigma sp., showed no glycosylation action against 1.

Figure 1.

Biotransformation of 2-fluorophenol (1) to 2-fluorophenyl β-D-glucoside (4) by cultured and immobilized cells of A. crassum.

In addition, 2-fluorophenol (1) was subjected to the biotransformation by immobilized A. crassum cells with sodium alginate. Fig. 2 shows that the glucosylation activity of immobilized cells was enhanced at 2% sodium alginate concentration. Immobilized A. crassum cells, which had been prepared at 2% sodium alginate concentration, were used for biotransformation experiments. After 48 h incubation of 2-fluorophenol (1), 2-fluorophenyl β-D-glucoside (140 μg/g cells) was obtained in higher yield in comparison with the case of the biotransformation using planktonic cells. Repetitive use of the immobilized cells was carried out. Yields of the product 4 obtained after each batch reaction were shown in Table 2. Experiments were repeated three times, and average is shown in Table 2. In repetitive batch use, the immobilized cells of A. crassum maintained the potential for the glucosylation of 1 (100 μg/g cells) after 5 times of usage.

Figure 2.

Effects of sodium alginate concentration on the glucosylation activity of the immobilized cells of A. crassum against 2-fluorophenol (1). Concentration (μg/g cells) of 2-fluorophenyl β-D-glucoside (4) (♦) is plotted.

Table 2.

The production of 4 by immobilized A. crassum.

Batch	Conc. of products (μg/g cells)a
1	147
2	143
3	123
4	117
5	90

Note:

Results are expressed as average of three times experiments.

Next, A. crassum cells were incubated with 3-fluorophenol (2) for 48h in the same biotransformation conditions as 2-fluorophenol (1). Glucosylation product was isolated from the cell cultures of A. crassum by preparative HPLC and was identified as 3-fluorophenyl β-D-glucoside (5, 20 μg/g cells) by spectroscopic methods (Fig. 3). Use of the immobilized A. crassum cells, which had been prepared at 2% sodium alginate concentration, improved the conversion yield of the product to 60 μg/g cells. When the substrate 4-fluorophenol (3) was used for the biotransformation experiment, 4-fluorophenyl β-D-glucoside (6) was obtained in 40 μg/g cells (Fig. 4). Incubation of immobilized A. crassum cells prepared at 2% sodium alginate concentration with 4-fluorophenol (3) afforded 4-fluorophenyl β-D-glucoside (6) in 100 μg/g cells.

Figure 3.

Biotransformation of 3-fluorophenol (2) to 3-fluorophenyl β-D-glucoside (5) by cultured and immobilized cells of A. crassum.

Figure 4.

Biotransformation of 4-fluorophenol (3) to 4-fluorophenyl β-D-glucoside (6) by cultured and immobilized cells of A. crassum.

This study demonstrated that the cultured cells of A. crassum can convert 2-, 3-, and 4-fluorophenols into the corresponding β-D-glucosides. Highest yield was found in the case of the biotransformation of 2-fluorophenol with ortho-phenolic hydroxyl group. Results of this experiment revealed that cultured cells of A. crassum can incorporate the environmentally toxic compounds such as 2-, 3-, and 4-fluorophenol and biotransform into β-D-glucosides. Yield of β-D-glucosides produced from fluorophenols by immobilized A. crassum cells in sodium alginate gel was improved in comparison with the case of biotransformation by planktonic A. crassum cells. Immobilized cells of A. crassum would be useful to detox fluorophenols to stable glycosides. This procedure is a simple operation and is environmentally friendly. Further studies on the enzymes which catalyze the glucosylation of fluorophenols are now in progress.