Recombinant Expression of Trametes versicolor Aflatoxin B1-Degrading Enzyme (TV-AFB1D) in Engineering Pichia pastoris GS115 and Application in AFB1 Degradation in AFB1-Contaminated Peanuts

Aflatoxins seriously threaten the health of humans and animals due to their potential carcinogenic properties. Enzymatic degradation approach is an effective and environmentally friendly alternative that involves changing the structure of aflatoxins. In this study, Trametes versicolor aflatoxin B1-degrading enzyme gene (TV-AFB1D) was integrated into the genome of Pichia pastoris GS115 by homologous recombination approach. The recombinant TV-AFB1D was expressed in engineering P. pastoris with a size of approximately 77 kDa under the induction of methanol. The maximum activity of TV-AFB1D reached 17.5 U/mL after the induction of 0.8% ethanol (v/v) for 84 h at 28 °C. The AFB1 proportion of 75.9% was degraded using AFB1 standard sample after catalysis for 12 h. In addition, the AFB1 proportion was 48.5% using AFB1-contaminated peanuts after the catalysis for 18 h at 34 °C. The recombinant TV-AFB1D would have good practical application value in AFB1 degradation in food crops. This study provides an alternative degrading enzyme for the degradation of AFB1 in aflatoxin-contaminated grain and feed via enzymatic degradation approach.


Introduction
Aflatoxins are pathogenic fungal toxins produced by Aspergillus flavus and A. parasiticus [1]. Aflatoxins and their producing bacteria are usually present in food products, feedstuffs, and agricultural raw materials [2]. Aflatoxins are a real threat to human and animal health due to their carcinogenicity and teratogenicity [3]. Among more than 20 kinds of aflatoxin derivatives, AFB 1 possesses the highest toxicity of liver cancer and immune system damage. AFB 1 causes carcinogenesis in the presence of the double bond of AFB 1 furan ring by inhibiting RNA synthesis [4]. The lactone ring of AFB 1 is the main toxicity site. The cleavage of lactone ring reduces the biological activity of AFB 1 with the formation of non-fluorescent compound [5]. In addition, a highly reactive AFB 1 -8,9-epoxide capable of reacting with DNA is produced under the activation of cytochrome P450 system [6,7].
Aflatoxins mainly pollute cereals, oils, and their products [8]. As an important agricultural raw material, peanut is directly in touch with A. flavus and A. parasiticus in the soil [9].
Peanut is highly susceptible to the contamination of aflatoxins. Aflatoxin-contaminated peanuts pollute the environment and cause the serious economic damage [10]. Despite remarkable improvements in the technologies of harvesting and storage processing, the contamination of aflatoxins is still a problem to be solved in the peanut industry [11]. Various physical, chemical, and biological methods have been developed to solve the problem of aflatoxin pollution [12]. The physical approach mainly includes heating treatment [13], UV radiation [14], high temperature [15], and adsorption [16]. The main disadvantages are long treatment time and low degradation rate [17,18]. The chemical methods include oxidant treatment and acid-base method by destroying the structure of aflatoxins [19,20]. Further, both the physical and chemical methods could reduce the quality of nutrition by changing the characteristics of raw materials [21].
Currently, the enzymatic degradation approach has been developed for its high specificity and efficiency of catalysis [22]. Laccase [23], peroxidase [24], and reductase [25] have been proved to be capable of degrading aflatoxins. The edible vegetable oils are vulnerable to aflatoxin pollution in the production process due to the raw materials and processing properties. Aflatoxin B 1 is one of the most common toxic substances in edible vegetable oil. Recently, the quality and safety of edible vegetable oils has attracted great attention of China State Council and the State Food and Drug Administration. The government is concentrating R&D efforts to solve the problem of aflatoxin pollution.
Trametes versicolor is a common polypore mushroom found throughout the world and is also a well-known traditional medicinal mushroom, one that is found growing on tree trunks. We cloned AFB 1 -degrading enzyme gene from Trametes versicolor (TV-AFB 1 D) according to Genbank accession number txid717944 in NCBI. TV-AFB 1 D was expressed in engineering E. coli BL21(DE3) with TV-AFB 1 D activity of 9.3 U/mL (not reported). To further investigate the effectiveness of expression, we integrated TV-AFB 1 D into the genome of P. pastoris GS115 in this study. In addition, the application of TV-AFB 1 D for degradation was also investigated in AFB 1 -contaminated peanuts. This study provides a new AFB 1 -degrading enzyme for application in enzymatic degradation in the food and feed industry.

TV-AFB 1 D Cloning and Evolutionary Tree Analysis
Aflatoxin B 1 -degrading enzyme TV-AFB 1 D from T. versicolor was cloned by using the designed primers with RT-PCR technique ( Figure 1). The size of TV-AFB 1 D was 2100 bp according to electrophoresis analysis and sequencing confirmation. The evolutionary tree analysis of TV-AFB 1 D with AFB 1 degradation enzymes from other species is shown in Figure 2. TV-AFB 1 D had closer genetic distance with Trametes coccinea than other aflatoxindegrading enzymes from Dichomitus squalens, Polyporus arcularius, Lentinus tigrinus, and Laetiporus sulpbureus. All the aflatoxin-degrading enzymes from Trametes genus belonging to family Polyporaceae speculated that aflatoxin-degrading enzymes would have common traits according to the result of evolutionary tree analysis.
problem of aflatoxin pollution [12]. The physical approach mainly includes ment [13], UV radiation [14], high temperature [15], and adsorption [16]. Th vantages are long treatment time and low degradation rate [17,18]. The chem include oxidant treatment and acid-base method by destroying the structur [19,20]. Further, both the physical and chemical methods could reduce the trition by changing the characteristics of raw materials [21].
Currently, the enzymatic degradation approach has been developed for ificity and efficiency of catalysis [22]. Laccase [23], peroxidase [24], and reduc been proved to be capable of degrading aflatoxins. The edible vegetable oil ble to aflatoxin pollution in the production process due to the raw mate cessing properties. Aflatoxin B1 is one of the most common toxic substances etable oil. Recently, the quality and safety of edible vegetable oils has attra tention of China State Council and the State Food and Drug Administration ment is concentrating R&D efforts to solve the problem of aflatoxin pollutio Trametes versicolor is a common polypore mushroom found throughout is also a well-known traditional medicinal mushroom, one that is found gr trunks. We cloned AFB1-degrading enzyme gene from Trametes versicolor (T cording to Genbank accession number txid717944 in NCBI. TV-AFB1D wa engineering E. coli BL21(DE3) with TV-AFB1D activity of 9.3 U/mL (not rep ther investigate the effectiveness of expression, we integrated TV-AFB1D in of P. pastoris GS115 in this study. In addition, the application of TV-AFB1D fo was also investigated in AFB1-contaminated peanuts. This study provides degrading enzyme for application in enzymatic degradation in the food an try.

TV-AFB1D Cloning and Evolutionary Tree Analysis
Aflatoxin B1-degrading enzyme TV-AFB1D from T. versicolor was clone designed primers with RT-PCR technique ( Figure 1). The size of TV-AFB1D according to electrophoresis analysis and sequencing confirmation. The evo analysis of TV-AFB1D with AFB1 degradation enzymes from other specie Figure 2. TV-AFB1D had closer genetic distance with Trametes coccinea than o degrading enzymes from Dichomitus squalens, Polyporus arcularius, Lentinu Laetiporus sulpbureus. All the aflatoxin-degrading enzymes from Trametes ge to family Polyporaceae speculated that aflatoxin-degrading enzymes wou mon traits according to the result of evolutionary tree analysis.

Expression Vector Construction of TV-AFB1D
TV-AFB1D was integrated into pPIC9K-His vector by double digestion techniques. The constructed recombinant plasmid was identified by the double digestion of Sna B I and Not I. Two bands after digestion possessed the size of approximately 9300 and 2100 bp ( Figure 3A). The confirmed recombinant vector was named pPIC9K-His-AFB1D after confirmation by gene sequencing ( Figure 3B).

Transformation of TV-AFB1D into P. pastoris GS115
The P. pastoris transformants were cultured on the plates with MD media after transformation. The transformants were transferred to the plates equipped with MM media (Figure 4). The transformants were identified with the designed primers for TV-AFB1D amplification. P. pastoris GS115 transformants with His + Mut + type for methanol utilization were integrated by pPIC9K-His-AFB1D according to the growth on the plates containing MD and MM media.

Expression Vector Construction of TV-AFB1D
TV-AFB1D was integrated into pPIC9K-His vector by double digestion techniques. The constructed recombinant plasmid was identified by the double digestion of Sna B I and Not I. Two bands after digestion possessed the size of approximately 9300 and 2100 bp ( Figure 3A). The confirmed recombinant vector was named pPIC9K-His-AFB1D after confirmation by gene sequencing ( Figure 3B).

Transformation of TV-AFB1D into P. pastoris GS115
The P. pastoris transformants were cultured on the plates with MD media after transformation. The transformants were transferred to the plates equipped with MM media ( Figure 4). The transformants were identified with the designed primers for TV-AFB1D amplification. P. pastoris GS115 transformants with His + Mut + type for methanol utilization were integrated by pPIC9K-His-AFB1D according to the growth on the plates containing MD and MM media.

Transformation of TV-AFB 1 D into P. pastoris GS115
The P. pastoris transformants were cultured on the plates with MD media after transformation. The transformants were transferred to the plates equipped with MM media ( Figure 4). The transformants were identified with the designed primers for TV-AFB 1 D amplification. P. pastoris GS115 transformants with His + Mut + type for methanol utilization were integrated by pPIC9K-His-AFB 1 D according to the growth on the plates containing MD and MM media.

Recombinant TV-AFB1D Expression in P. pastoris GS115
The recombinant TV-AFB1D was expressed by engineering P. pastoris GS115 with the size of approximately 77 kDa under the induction of 0.8% methanol. No TV-AFB1D was detected by the wild-type P. pastoris GS115 according to SDS-PAGE analysis ( Figure 5). The highest activity of TV-AFB1D was 17.5 U/mL after the induction of 0.8% methanol (v/v) for 84 h at 30 °C. No TV-AFB1D activity of the fermentation broth from the wild-type P. pastoris GS115 was detected under the same treatment conditions ( Figure 6). Therefore, the recombinant TV-AFB1D could express in engineering P. pastoris GS115.

Recombinant TV-AFB 1 D Expression in P. pastoris GS115
The recombinant TV-AFB 1 D was expressed by engineering P. pastoris GS115 with the size of approximately 77 kDa under the induction of 0.8% methanol. No TV-AFB 1 D was detected by the wild-type P. pastoris GS115 according to SDS-PAGE analysis ( Figure 5). The highest activity of TV-AFB 1 D was 17.5 U/mL after the induction of 0.8% methanol (v/v) for 84 h at 30 • C. No TV-AFB 1 D activity of the fermentation broth from the wild-type P. pastoris GS115 was detected under the same treatment conditions ( Figure 6). Therefore, the recombinant TV-AFB 1 D could express in engineering P. pastoris GS115.

Recombinant TV-AFB1D Expression in P. pastoris GS115
The recombinant TV-AFB1D was expressed by engineering P. pastoris GS115 with the size of approximately 77 kDa under the induction of 0.8% methanol. No TV-AFB1D was detected by the wild-type P. pastoris GS115 according to SDS-PAGE analysis ( Figure 5). The highest activity of TV-AFB1D was 17.5 U/mL after the induction of 0.8% methanol (v/v) for 84 h at 30 °C. No TV-AFB1D activity of the fermentation broth from the wild-type P. pastoris GS115 was detected under the same treatment conditions ( Figure 6). Therefore, the recombinant TV-AFB1D could express in engineering P. pastoris GS115.

Effect of Methanol Concentration and Time on the TV-AFB 1 D Expression
The effects of induction time and methanol concentration on TV-AFB 1 D activity were investigated (Figure 7). The highest activities of TV-AFB 1 D expressed by the recombinant P. pastoris GS115 were achieved after induction for 84 h and in the presence of 0.8% methanol (v/v). In particular, the activities of TV-AFB 1 D were substantially decreased with the addition of 1.2% and 0.5% of methanol. Therefore, the optimum methanol concentration and treatment time were 0.8% and 84 h for the inducible expression of TV-AFB 1 D, respectively.

Effect of Methanol Concentration and Time on the TV-AFB1D Expression
The effects of induction time and methanol concentration on TV-AFB1D activity were investigated ( Figure 7). The highest activities of TV-AFB1D expressed by the recombinant P. pastoris GS115 were achieved after induction for 84 h and in the presence of 0.8% methanol (v/v). In particular, the activities of TV-AFB1D were substantially decreased with the addition of 1.2% and 0.5% of methanol. Therefore, the optimum methanol concentration and treatment time were 0.8% and 84 h for the inducible expression of TV-AFB1D, respectively.

Effect of Temperatures and Treatment Time on the Expression of TV-AFB1D
The effects of temperatures and treatment time on TV-AFB1D expression are shown in Figure 8. The TV-AFB1D activities reached the highest after induction for 84 h. The highest activity of TV-AFB1D was 16.5 U/mL at 28 °C among all the set temperatures of 25-32 °C. Therefore, the optimum temperature and time were 28 °C and 84 h for the inducible expression of TV-AFB1D in engineering P. pastoris GS115, respectively.

Effect of Methanol Concentration and Time on the TV-AFB1D Expression
The effects of induction time and methanol concentration on TV-AFB1D activity were investigated (Figure 7). The highest activities of TV-AFB1D expressed by the recombinant P. pastoris GS115 were achieved after induction for 84 h and in the presence of 0.8% methanol (v/v). In particular, the activities of TV-AFB1D were substantially decreased with the addition of 1.2% and 0.5% of methanol. Therefore, the optimum methanol concentration and treatment time were 0.8% and 84 h for the inducible expression of TV-AFB1D, respectively.

Effect of Temperatures and Treatment Time on the Expression of TV-AFB1D
The effects of temperatures and treatment time on TV-AFB1D expression are shown in Figure 8. The TV-AFB1D activities reached the highest after induction for 84 h. The highest activity of TV-AFB1D was 16.5 U/mL at 28 °C among all the set temperatures of 25-32 °C. Therefore, the optimum temperature and time were 28 °C and 84 h for the inducible expression of TV-AFB1D in engineering P. pastoris GS115, respectively.

Product Formation of AFB 1 -Contaminated Peanuts Catalyzed by TV-AFB 1 D
HPLC method was used to determine the product formation of AFB 1 catalyzed by the recombinant TV-AFB 1 D. As the control group, the AFB 1 standard possessed a special peak after running for 45 min at a wavelength of 365 nm (Figure 9). The profiles of catalytic products were determined by HPLC after the catalysis of AFB 1 -contaminated peanuts by the recombinant TV-AFB 1 D. With the exception of the AFB 1 standard, another peak was detected under a wavelength of 210 nm after running for 22 min. The result indicated that new product was formed under the catalysis of TV-AFB 1 D with AFB 1 as substrate. Toxins 2021, 13, x FOR PEER REVIEW 6 of 12

Product Formation of AFB1-Contaminated Peanuts Catalyzed by TV-AFB1D
HPLC method was used to determine the product formation of AFB1 catalyzed by the recombinant TV-AFB1D. As the control group, the AFB1 standard possessed a special peak after running for 45 min at a wavelength of 365 nm (Figure 9). The profiles of catalytic products were determined by HPLC after the catalysis of AFB1-contaminated peanuts by the recombinant TV-AFB1D. With the exception of the AFB1 standard, another peak was detected under a wavelength of 210 nm after running for 22 min. The result indicated that new product was formed under the catalysis of TV-AFB1D with AFB1 as substrate. Figure 9. Determination of catalytic products of AFB1 catalyzed by TV-AFB1D using HPLC approach. Note: a and b represent HPLC profiles before and after catalysis, respectively.

Effect of Time on the Residue of AFB1 Standard Sample
The effect of catalysis time on the residual proportion of the AFB1 standard sample was investigated at 32 °C ( Figure 10). The proportion of AFB1 residue substantially decreased from 100% to 27.8% for 5 h of catalysis with the degradation rate of 72.2%. During the next catalysis for 5-12 h, the proportion of residual AFB1 decreased slowly. The proportion of residual AFB1 standard sample was 24.1% after catalysis for 12 h with the degradation rate of 75.9%.

Product Formation of AFB1-Contaminated Peanuts Catalyzed by TV-AFB1D
HPLC method was used to determine the product formation of AFB1 catalyzed by the recombinant TV-AFB1D. As the control group, the AFB1 standard possessed a special peak after running for 45 min at a wavelength of 365 nm (Figure 9). The profiles of catalytic products were determined by HPLC after the catalysis of AFB1-contaminated peanuts by the recombinant TV-AFB1D. With the exception of the AFB1 standard, another peak was detected under a wavelength of 210 nm after running for 22 min. The result indicated that new product was formed under the catalysis of TV-AFB1D with AFB1 as substrate. Figure 9. Determination of catalytic products of AFB1 catalyzed by TV-AFB1D using HPLC approach. Note: a and b represent HPLC profiles before and after catalysis, respectively.

Effect of Time on the Residue of AFB1 Standard Sample
The effect of catalysis time on the residual proportion of the AFB1 standard sample was investigated at 32 °C ( Figure 10). The proportion of AFB1 residue substantially decreased from 100% to 27.8% for 5 h of catalysis with the degradation rate of 72.2%. During the next catalysis for 5-12 h, the proportion of residual AFB1 decreased slowly. The proportion of residual AFB1 standard sample was 24.1% after catalysis for 12 h with the degradation rate of 75.9%. Figure 9. Determination of catalytic products of AFB 1 catalyzed by TV-AFB 1 D using HPLC approach. Note: a and b represent HPLC profiles before and after catalysis, respectively.

Effect of Time on the Residue of AFB 1 Standard Sample
The effect of catalysis time on the residual proportion of the AFB 1 standard sample was investigated at 32 • C ( Figure 10). The proportion of AFB 1 residue substantially decreased from 100% to 27.8% for 5 h of catalysis with the degradation rate of 72.2%. During the next catalysis for 5-12 h, the proportion of residual AFB 1 decreased slowly. The proportion of residual AFB 1 standard sample was 24.1% after catalysis for 12 h with the degradation rate of 75.9%.

Effect of Time on the Proportion of AFB 1 Residue in Peanuts
The effect of treatment time on the proportion of AFB 1 residue in AFB 1 -contaminated peanuts was investigated at 32 • C (Figure 11). Within the initial 10 h, the proportion of AFB 1 residue decreased rapidly from 100% to 55.7%. After treatment for 18 h, the proportion of AFB 1 residue in AFB 1 -contaminated peanuts gradually decreased to 51.5% with the degradation rate of 48.5%. Therefore, the recombinant TV-AFB 1 D could effectively catalyze AFB 1 in AFB 1 -contaminated peanuts.

Effect of Time on the Proportion of AFB1 Residue in Peanuts
The effect of treatment time on the proportion of AFB1 residue in AFB1-contaminated peanuts was investigated at 32 °C ( Figure 11). Within the initial 10 h, the proportion of AFB1 residue decreased rapidly from 100% to 55.7%. After treatment for 18 h, the proportion of AFB1 residue in AFB1-contaminated peanuts gradually decreased to 51.5% with the degradation rate of 48.5%. Therefore, the recombinant TV-AFB1D could effectively catalyze AFB1 in AFB1-contaminated peanuts.

Effect of Temperature on the Proportion of AFB1 Residue in Peanuts
The effect of temperature on the proportion of AFB1 residue in AFB1-contaminated peanuts was investigated after catalysis for 5 h (Figure 12). In the range of 26 to 42 °C, the proportion curve of AFB1 residue was in the shape of a "V". The proportion of AFB1 residue gradually decreased during the temperatures of 26 to 34 °C and increased during the temperatures of 34 to 42 °C. The lowest concentration of AFB1 residue in AFB1-contaminated peanuts was 52.1% at 34 °C with a degradation rate of 47.9%. Too low and too high temperatures were not conducive to the degradation of AFB1 by TV-AFB1D in AFB1-contaminated peanuts.

Effect of Time on the Proportion of AFB1 Residue in Peanuts
The effect of treatment time on the proportion of AFB1 residue in AFB1-contaminated peanuts was investigated at 32 °C (Figure 11). Within the initial 10 h, the proportion of AFB1 residue decreased rapidly from 100% to 55.7%. After treatment for 18 h, the proportion of AFB1 residue in AFB1-contaminated peanuts gradually decreased to 51.5% with the degradation rate of 48.5%. Therefore, the recombinant TV-AFB1D could effectively catalyze AFB1 in AFB1-contaminated peanuts.

Effect of Temperature on the Proportion of AFB1 Residue in Peanuts
The effect of temperature on the proportion of AFB1 residue in AFB1-contaminated peanuts was investigated after catalysis for 5 h (Figure 12). In the range of 26 to 42 °C, the proportion curve of AFB1 residue was in the shape of a "V". The proportion of AFB1 residue gradually decreased during the temperatures of 26 to 34 °C and increased during the temperatures of 34 to 42 °C. The lowest concentration of AFB1 residue in AFB1-contaminated peanuts was 52.1% at 34 °C with a degradation rate of 47.9%. Too low and too high temperatures were not conducive to the degradation of AFB1 by TV-AFB1D in AFB1-contaminated peanuts.

Effect of Temperature on the Proportion of AFB 1 Residue in Peanuts
The effect of temperature on the proportion of AFB 1 residue in AFB 1 -contaminated peanuts was investigated after catalysis for 5 h (Figure 12). In the range of 26 to 42 • C, the proportion curve of AFB 1 residue was in the shape of a "V". The proportion of AFB 1 residue gradually decreased during the temperatures of 26 to 34 • C and increased during the temperatures of 34 to 42 • C. The lowest concentration of AFB 1 residue in AFB 1contaminated peanuts was 52.1% at 34 • C with a degradation rate of 47.9%. Too low and too high temperatures were not conducive to the degradation of AFB 1 by TV-AFB 1 D in AFB 1 -contaminated peanuts.

Discussion
Although the physical and chemical methods have been applied in the detoxification of aflatoxins, these approaches are difficult to meet the requirement of clean, safe, and environmentally friendly production [26]. Currently, the enzymatic degradation has been applied in the degradation of aflatoxins for its safety and specificity [27]. A large number of studies have been reported on the enzymes related to aflatoxin degradation (Table 1).

Discussion
Although the physical and chemical methods have been applied in the detoxification of aflatoxins, these approaches are difficult to meet the requirement of clean, safe, and environmentally friendly production [26]. Currently, the enzymatic degradation has been applied in the degradation of aflatoxins for its safety and specificity [27]. A large number of studies have been reported on the enzymes related to aflatoxin degradation (Table 1). Enzymes related to aflatoxin degradation include various catalytic properties of F 420 H 2 -dependent reductase [25], laccase [23], and peroxidase [24]. In addition, aflatoxindetoxifizyme (ADTZ) [28], AFB 1 -horse radish peroxidase (HRP) [29], Myxobacteria aflatoxin degradation enzyme (MADE) [30], Bacillus aflatoxin-degrading enzyme (BADE) [31], and Pantoea aflatoxin degradation enzyme (PADE) [32] also possess the capability of aflatoxin degradation. In the previous report, the catalytic performances of enzymes were identified by using AFB 1 standard sample as catalytic substrate. These enzymes were rarely used for degradation of aflatoxins in food and feed. In this study, T. versicolor aflatoxin B 1 -degrading enzyme gene was expressed in engineering P. pastoris. AFB 1 standard sample and AFB 1 -contaminated peanuts were used to detect the degradation effect of AFB 1 . The AFB 1 proportions of 75.9% and 48.5% were degraded using AFB 1 standard sample and AFB 1 -contaminated peanuts as substrates, respectively. Table 1. Aflatoxin-degrading enzymes and catalysis performances.

Conclusions
In this study, the recombinant TV-AFB 1 D with a size of 77 kDa was effectively expressed by engineering P. pastoris. The optimal temperature and methanol concentration were 28 • C and 0.8% for the inducible expression of TV-AFB 1 D, respectively. The proportion of residual AFB 1 standard sample was 24.1% after catalysis for 12 h with a degradation rate of 75.9%. In addition, the proportion of AFB 1 residue in AFB 1 -contaminated peanuts decreased to 51.5% with a degradation rate of 48.5% after treatment for 18 h at 34 • C. This study provided an alternative TV-AFB 1 D degradation enzyme for the removal of AFB 1 in food products and agricultural raw materials.

Materials and Reagents
Vector pPIC9K-His, TV-AFB 1 D gene, P. pastoris GS115, and T. versicolor were stored in the Experimental Center of Hefei University of Technology. Gene sequencing and primer synthesis were performed by Sangon Biotech. Taq polymerase, Stu I, Not I, and SnaB I were from NEB Company. Gel imaging systems, sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE), polymerase chain reaction (PCR) amplification, and electrophoresis devices were manufactured by Bio-RAD Company. ProteinIsoNi-IDA resin and AFB 1 immunoaffinity column were from Transgen Biotech and Welch Company, respectively.

Construction of pPIC9K-His-TV-AFB 1 D Vector
TV-AFB 1 D encoding aflatoxin degradation enzyme was cloned by reverse transcription PCR (RT-PCR) technique according to Genbank accession number txid717944 in the National Center for Biotechnology Information (NCBI). The sequences of restriction endonuclease SnaB I and Not I were added in the corresponding primers for the amplification of TV-AFB 1 D. The corresponding primers were designed as follows: F: 5 -GGGAAATACGTAATGGCTCGCGCGAAGTACTC-3 (SnaB I); R: 5 -GGGAAAGCGGCCGC TTAAAGCTTCCGCTCTATGA3 (Not I). Both the product of amplification and pPIC9K-His vector were double digested by SnaB I and Not I. The recovered gene was ligated by T 4 ligase to produce vector pPIC9K-His-AFB 1 D. pPIC9K-His-AFB 1 D was confirmed by PCR amplification, double-enzyme digestion identification, and gene sequencing.

Transformation of pPIC9K-His-TV-AFB 1 D into P. pastoris GS115
The linearized pPIC9K-His-AFB 1 D was digested by Stu I and integrated into P. pastoris GS115 by electroporation transformation method [37]. P. pastoris GS115 had a mutation in histidine dehydrogenase (his4) and could not synthesize histidine. pPIC-9K-His contained his4 gene that was complementary to the host. The transformants were screened on the plate equipped with histidine-free medium. The recombinant P. pastoris with His + Mut + phenotype grew on minimal methanol medium (MM) plates in the presence of methanol. The transformants were screened out using the solid plates containing minimal dextrose medium (MD) and MM. The true transformants were further confirmed by PCR identification and gene sequencing.

Inducible Expression and Condition Optimizations of TV-AFB 1 D
The His + Mut + phenotype-positive clones were incubated with the shaking speed of 200 rpm at 30 • C. The collected cells of recombinant P. pastoris were mixed with methanolcomplex buffer medium. The transformants were incubated at 30 • C with the shaking speed of 200 rpm. The fermentation broth was added with 0.8% methanol (v/v) every 24 h for the induction of recombinant TV-AFB 1 D. The parameters of temperatures, methanol concentrations, and time were optimized to enhance the inducible expression of TV-AFB 1 D.

Purification of Recombinant TV-AFB 1 D and Definition of Activity
The recombinant TV-AFB 1 D was purified by pre-equilibration with Ni 2+ -chelate affinity chromatography column and elution with imidazole eluent with ProteinIso Ni-IDA resin. The profile of TV-AFB 1 D protein was analyzed by SDS-PAGE. The unit of TV-AFB 1 D activity was defined as the amount of enzyme that catalyzed the consumption of 1 nmoL AFB 1 per minute. The activity of TV-AFB 1 D was calculated by using the formula of (M 0 − M 1 )/(312 × t × V), where M 0 , M 1 , t, and V represent the AFB 1 weight in the control and experimental groups (µg), reaction time (min), and enzyme amount (mL), respectively; 312 indicates the molecular weight of AFB 1 .

Measurement of AFB 1 Content and Degradation Products
The content of AFB 1 was detected by HPLC using the following process parameters: methanol-to-water ratio of 40/60, isocratic elution, ultraviolet (UV) detector, C 18 Shimpack VP-ODS (5 µm, 250 mm × 4.6 mm), C 18 reverse column, 0.7 mL/min of flow rate, 190-400 nm of detection wavelength, and 30 • C of column temperature. The signal of AFB 1 was detected by the UV detector at a wavelength of 365 nm. The amount of AFB 1 was calculated on the basis of the peak areas with the AFB 1 standard sample as the control.

Application in the AFB 1 Degradation of AFB 1 -Contaminated Peanuts
The AFB 1 -contaminated peanuts were immersed in the solution containing the recombinant TV-AFB 1 D from engineering P. pastoris GS115. After incubation for 12 h, the recovered peanuts were soaked with methanol solution containing 40% of water (v/v). Then, the supernatant was purified through the AFB 1 immunoaffinity column with the flow rate of 2 drops per second. The collected eluate was further purified by the filtration with 0.22 µm size of filter membrane. The effects of treatment time and temperature on the degradation efficiency of AFB 1 -contaminated peanuts by TV-AFB 1 D were investigated.

Data Analysis
The data were statistically given with three replicates. Origin and SPSS software were used to analyze the data with mean ± standard deviation.