Batch Mode Reactor for 3,5-Dinitrosalicylic Acid Degradation by Phanerochaete chrysosporium

Abstract

A new batch mode reactor was constructed to conduct continuous biodegradation of 3,5-dinitrosalicylic acid. Various types of matrices with immobilized Phanerochaete chrysosporium were immersed in a solution containing pollutant and mineral nutrients. Three parameters were chosen to optimize the process. The nitrate and nitrite ions concentrations and HPLC analysis were used to prove the biodegradation of 3,5-dinitrosalicylic acid, and the mixed effects model using one-factor ANOVA was used for statistical calculations. The results showed the correlation between the initial pH, a medium composition, and the process time. In pH = 6.5, the degradation effectiveness was estimated at 99% decrease in the substrate within 14 days, while an 80% decrease of acid concentration was indicated in pH = 3.5 after 28 days of the process duration.

1. Introduction

Nitroaromatic compounds have been produced and used primarily as explosives materials for many years [1]. The presence of –NO₂ groups determine their high toxic and cancerogenic properties [2]. 3,5-Dinitrosalicylic acid (3,5-DNS acid) classified as a hazardous waste and listed in the European Catalogue on Hazardous Waste with the codes 06.01.06 and 06.10.02.3 is one of the representatives of this chemical group [3]. 3,5-DNS acid has been used for years as the main reagent in laboratories for the analysis of sugars in reducing reactions [4]. The improper storage and utilization of 3,5-DNS acid influences environmental pollution.

To minimize the contamination effect of nitroarenes on the environment, several methods were proposed. They were based on physicochemical and chemical reactions with hydrogen peroxide or ozone, Fenton’s reagent in oxidation or UV radiation, incineration, or sonolysis [5,6,7,8,9]. These processes are often supported by physical treatments like coagulation, adsorption, or filtration [10]. The chemical and physicochemical methods have limited efficiency and generate a high cost of utilization. Nevertheless, there is a group of microorganisms which developed metabolic pathways for degradation of these pollutants. The white rot fungi to which Phanerochaete chrysosporium has been classified produces enzymes that are able to decompose nitroaromatic compounds including 3,5-DNS acid. They can reduce nitro group to the amine derivative as well as divide the aromatic ring to the aliphatic chain via enzymatic oxidation [11,12].

The aim of our research is to present a new process of 3,5-dinitrosalicylic acid degradation by Phanerochaete chrysosporium in a batch reactor that works at a micro-industrial scale. The scientific literature reports that nitrocompounds, including 3,5-DNS acid, biodegrade in stationary culture conditions. Our research allows for the improvement of biodegradation efficiency as well as a reduction in time for the process.

2. Materials and Methods

2.1. Materials

2.1.1. Biological Material

The microorganisms used in our research were Phanerochaete chrysosporium Burdsall ATCC 34,511, which originated from the Lodz Centre Culture Collection (LOCK) and were deposited in the Institute of Molecular and Industrial Biotechnology at Lodz University of Technology.

The basidiomycete was inoculated and stored on the 3% agar maltose slants enriched with 5 wt% of oat meals. Two weeks before starting the experiment, the strain was activated in a wort medium (peptones 15 g/dm³, yeast extract 3 g/dm³, NaCl 6 g/dm³, and D(+)-glucose 1 g/dm³) in the temperature 37 °C for one week in aerobic condition. Next, 5 cm³ of the Phanerochaete chrysosporium inoculum (OD 660 = 0.3) was added to each flask to allow the biomass to grow before starting the flow culture experiment.

2.1.2. Immobilization Matrices

The matrices used in the continuous flow cultures for biomass immobilization were as follows:

• Beech smoking chips of BROWIN Company, Poland, consisting of cellulose (41 wt%), hemicellulose (33 wt%), lignin (22% wt%), and other substances (4 wt%) [13];
• Sugar beet pulp originating from sugar beet processes as the by-products used in the form of a briquette which comprises carbohydrates (75 wt%) and nitrogen (9 wt%) [14]; and
• Polyurethane foam—block samples at sizes 1 cm³ × 1 cm³ × 1 cm³ of polyether polyol foam (EUROFOAM Company). The polyurethane foam was free of nutrients. To prepare the culture condition which could be compared to the samples including the other matrices, it was necessary to enrich this culture with the source of polysaccharides. The citrus peels were chosen as a natural source of dietary fibres (about 65 wt%) [15,16].

The Erlenmeyer’s flasks were filled up with 60% v/v matrices and soaked up in the water (40% v/v). After sterilization (20 min in 121 °C under a pressure of 0.1 MPa), 5 cm³ of the Phanerochaete chrysosporium inoculum (OD 660 = 0.3) was added to each flask to initiate the biomass growth before starting the flow culture experiment. The incubation lasted 6 weeks in a temperature of 37 °C in aerobic condition.

2.1.3. The 3,5-Dinitosalicylic Acid

3,5-dinitrosalicylic acid (3,5-DNS) from Sigma-Aldrich (St. Louis, MO, USA) was used in our research. Its CAS number was 609-99-4, and the purity was 98.4%.

2.2. Methods

2.2.1. Continuous Culture Condition

The biodegradation process was conducted at a micro-industrial scale in the batch reactor (Figure 1) [17]. At the beginning, the peristaltic pump (2) was started by dispensing the liquid dose onto the immobilizing matrix containing microorganisms. The matrix was placed into the reactor (vessel 1) with a nominal capacity of 100 cm³.

Simultaneously, four 500 cm³ containers (4) were filled with the chosen liquid media (regular or enriched with mineral salts). The containers were placed in a water bath while maintaining a constant temperature of 37 °C. Then, after 6 weeks of immobilizing microorganisms, the peristaltic pump (2) supplied the medium from reactor (vessel) (1) to the container (4) at initial volumetric flow equals 1.4 × 10⁻⁴ dm³/s. During the experiments, the flow output was maintained at the same rate. In addition, an aerator (3) was used to allow conduction of the process under aerobic conditions at both ports of the reactor at the inlet (6) and outlet (8), respectively. The potassium manganate (VII) solution with a concentration of 1 mol/dm³ was used to hold the air sterility.

Two types of media were applied during the experiment. The first medium (A) consisted of distilled water, 0.1% v/v of the 3,5-DNS acid with the concentration of 4.0 × 10⁻³ mol/dm³, and 5.0 × 10⁻² mol/dm³ citric buffer which allowed for starting the cultures in various pH conditions: 3.5, 4.5, 5.5, or 6.5. The studies also considered three immobilization matrices as the experimental samples: A1—medium A flowing beech smoking chips; A2—medium A flowing a sugar beet pulp; and A3—medium A flowing a polyurethane foam. The second medium solution (B) used in the process consisted of the first medium (A) supplemented by the modified Czapek medium [18]. The potassium nitrate was substituted by 1.0 g/dm³ ammonium sulphate. Additionally, the glucose solution with an approximate concentration of 3.2 g/dm³ was added. The samples of this experimental part were B1—medium B flowing the beech smoking chips; B2—medium B flowing a sugar beet pulp; and B3—medium B flowing a polyurethane foam. After 28 days, the process was stopped and the liquid samples were collected for chemical analyses.

2.2.2. Chemical Analysis

Every seven days, the samples were collected for chemical analysis. The pH measurements were done using the Elmetron CP-505 pH-meter with temperature compensation. The nitrate and nitrite ions concentrations were measured using QUANTOFIX test straps at the concentration ranges 10–500 mg/dm³ of NO₃⁻ and 1–80 mg/dm³ of NO₂⁻.

The High-Performance Liquid Chromatography (HPLC) Analysis of 3,5-DNS Acid

The samples were subjected to liquid–liquid extraction against ethyl acetate (analytical grade, POCH) three times in 2:1 liquid–extractant ratio. Then, the extract was evaporated under a vacuum and dissolved in acetonitrile (HPLC grade, SIGMA-ALDRICH). The extracted 3,5-DNS acid was analysed using a Dionex 5110 with C18 RP Phenomenex 250 mm × 4.60 mm × 5 μm column with a detector Dionex UVD 340S set to λ = 210 nm. Mobile phase (isocratic conditions) consisted of 0.1% acetic acid solution (HPLC grade, SIGMA-ALDRICH) of ultrapurified water and acetonitrile (HPLC, SIGMA-ALDRICH) in a 30:70 ratio.

2.3. Statistical Calculations

The statistical calculations and presentation of the results were done using Statictica 12 (StatSoft, Tulsa, OK, USA).

3. Results and Discussion

To optimize the process, we focused on three factors: the type of immobilization matrix, the mineral composition of the liquid media, and the initial culture acidity (pH).

The results obtained in our research proved that the initial composition of the process medium and its initial acidity significantly influenced the biodegradation effect (Figure 2). In strongly acidic conditions (pH = 3.5), the degradation process was not effective within the investigated time while an initial pH higher than 4.5 intensified the process. The most effective decomposition of 3,5-DNS acid (over 90%) was observed at the second week of the process in the samples with initial pHs 5.5 and 6.5. The results showed that the type of immobilization matrix did not determine the process effectiveness significantly.

In our previous research concerning 3,5-DNS acid biodegradation by Phanerochaete chrysosporium in stationary condition cultures, the substrate’s concentration decreased after the third week of the process [19]. The most effective degradation level did not exceed 55% of the initial concentration of 3,5-DNS acid (8 × 10⁻⁴ mol/dm³).

To prove 3,5-DNS acid is decomposed by basidiomycetes, we started with the identification of nitrate and nitrite ions that should appear in the medium solution during biodegradation. Figure 3 and Figure 4 show the tests results which confirm high both nitrate and nitrite ions concentrations levels in the enriched medium cultures in which the initial pHs were 5.5 and 6.5.

The HPLC analyses confirmed the presence of intermediate products of 3,5-DNS acid (1) which appeared during the enzymatic decomposition (

Table 1. The compounds identified during various stages of 3,5-DNS acid biodegradation.

No	m/z	Retention Time [min]	Name of Substrate and by Products
1	227	1.86	the 3,5-dinitrosalicylic acid
2	197	2.74	the 3-amino-5-nitrosalicylic acid
3	183	2.16	the 2,4-dinitrophenol
4	153	2.24	the 2-amino-4-nitrophenol
5	141	2.31	the 1-amino-2,4,5-trihydroxybenzene

).

There were two possibilities of the 3,5-DNS acid initial decomposition (Figure 5): by C1 ring decarboxylation or by the reduction of the −NO₂ group linked to C3 in an acid molecule [20]. The by-products that appeared were 3-amino-5-nitrosalicylic acid (2) and 2,4-dinitrophenol (3). The 2-amino-4-nitrophenol appeared as the third common by-product (4). Next, the nitro groups linked to C5 and C6 were replaced by the hydroxyl groups which caused the appearance of the 1-amino-2,4,5-trihydroxybenzene (5). The next step in the enzymatic oxidation was ring decomposition to the aliphatic chain by-products.

The enzyme system of Phanerochaete chrysosporium characterized by broad spectrum enzyme production consisted of membrane-bound cyto-chrome P450-related proteins, dioxygenases, nitrobenzene nitroreductase (E.C. 1.7.1.16), lignin peroxidase LiP (E.C. 1.11.1.14), manganese-dependent peroxidase MnP (E.C. 1.11.1.13), and laccase (E.C.1.10.3.2) that catalyse the decomposition of chloropesticides, nitroarenes, or aryl alcohols [21,22,23,24]. Lignin peroxidase (LiP) synthesized by Phanerochaete chrysosporium is one of the enzymes directly involved 3,5-DNS acid biodegradation which dominated in the first stages of molecule oxidation by 3-amino-5-nitrosalicylic acid or 2,4-dinitrophenol to obtain 2-amino-4-nitrophenol.

The process was intensified by the presence of nutrients in the culture medium such as cellulose and hemicelluloses as well as aromatic alcohols that may have been released through the breakdown of lignin [25]. The alcohols could slow down the catalytic decomposition of 3,5-DNS acid due to the co-substrates of enzymes degrading nitrocompounds. The presence of Mn(II) ions influenced biomass growth as well as manganese-dependent peroxidase (MnP) and lignin peroxidase (LiP) synthesis and their activities [26,27].

In order to confirm the hypothesis concerning the influence of three chosen parameters on 3,5-DNS acid biodegradation, statistical calculations were also performed. The first-order (noninteractive) ANOVA main effects analysis as well as the post-hoc Duncan’s test were used. The results proved that the medium composition, the initial pH, and the type of matrix significantly influenced the changing substrate concentrations during the process (Figure 6).

The chemical analyses and statistic calculations proved that parameters like the type of immobilization matrix, the mineral composition of the liquid media, and the initial pH caused high process effectiveness conducted in the batch reactor.

4. Conclusions

The results obtained in our research proved that Phanerochaete chrysosporium is able to degrade 3,5-dinitrosalicylic acid. Phanerochaete chrysosporium was able to decompose 3,5-dinitrosalicylic acid under proper conditions to fully degrade a 4 × 10⁻³ mol/dm³ solution of the substrate within 14 days. The reactor was operated in aatch mode until the assumed reduction of the 3,5-dinitrosalicylic acid was achieved.

All the tested parameters (the mineral composition, the initial pH of the cultures, as well as the type of immobilization matrix) were important for efficient biodegradation. The most effective results of the biodegradation in a batch mode reactor working at a micro-industrial scale guaranteed the culture condition in the enriched medium with an initial pH of 6.5 with microorganisms immobilized on the sugar beet pulp and the polyurethane foam. The obtained results are fundamental for implementing the process on the industrial scale and for application in wastewater treatment.