Application of Composite Bars in Wooden, Full-Scale, Innovative Engineering Products-Experimental and Numerical Study.

The commercialization of modular timber products as cost-effective and lightweight components has resulted in innovative engineering products, e.g., glued laminated timber, laminated veneer lumber, I-beams, cross-laminated timber and solid timber joined with wedge joints. With the passage of time, timber structures can deteriorate, or new structural elements are required to increase the stiffness or load-bearing capacity in newly built structures, e.g., lintels over large-scale glazing or garages, or to reduce cross-sectional dimensions or save costly timber material while still achieving low weight. It is in such cases that repair or correct reinforcement is required. In this experimental and numerical study, the static performance of flexural timber beams reinforced with prestressed basalt BFRP, glass GFRP and hybrid glass-basalt fiber bars is shown. The experimental tests resulted in an increase in the load-carrying capacity of BFRP (44%), GFRP (33%) and hybrid bars (43%) and an increase in the stiffness of BFRP (28%), GFRP (24%) and hybrid bars (25%). In addition to this, glued laminated timber beams reinforced with prestressed basalt rods subjected to biological degradation, 7 years of weathering and prolonged exposure to various environmental conditions were examined, and an increase in the load-bearing capacity of 27% and an increase in stiffness of 28% were obtained. In addition, full-size laminated timber beams reinforced with prestressed basalt bars were investigated in the field as an exploratory test under fire conditions at elevated temperatures, and the effect of the physical-mechanical properties during the fire was examined via an analysis of these properties after the fire. In addition, a satisfactory correlation of the numerical simulations with the experimental studies was obtained. The differences were between 1.1% and 5.5%. The concordance was due to the fact that, in this study, the Young, Poisson and shear moduli were determined for all quality classes of sawn timber. Only a significant difference resulted in the numerical analysis for the beams exposed to fire under fire conditions. The experimental, theoretical and numerical analyses in this research were exploratory and will be expanded as directions for future research.

Degradation Mechanism of Aflatoxin M1 by Recombinant Catalase from Bacillus pumilusE-1-1-1: Food Applications in Milk and Beer.

A bacteria capable of degrading aflatoxin M1 (AFM1) was isolated from African elephant manure. It was identified as Bacillus pumilus by 16s rDNA sequencing and named B. pumilusE-1-1-1. Compared with physical and chemical methods, biological methods have attracted much attention due to their advantages, such as thorough detoxification, high specificity, and environmental friendliness. This work aimed to study the effects of a recombinant catalase (rCAT) from B. pumilusE-1-1-1 on the degradation of AFM1 in pattern solution. The degradation mechanism was further explored and applied to milk and beer. Kinetic Momentum and Virtual Machine Maximum values for rCAT toward AFM1 were 4.1 µg/mL and 2.5 µg/mL/min, respectively. The rCAT-mediated AFM1 degradation product was identified as C15H14O3. Molecular docking simulations suggested that hydrogen and pi bonds played major roles in the steadiness of AFM1-rCAT. In other work, compared with identical density of AFM1, survival rates of Hep-G2 cells incubated with catalase-produced AFM1 degradation products increased by about 3 times. In addition, degradation rates in lager beer and milk were 31.3% and 47.2%, respectively. Therefore, CAT may be a prospective substitute to decrease AFM1 contamination in pattern solution, milk, and beer, thereby minimizing its influence on human health.

Enhanced aerobic granular sludge with micro-electric field for sulfamethoxazole degradation: Efficiency, mechanism, and microbial community.

In this study, an aerobic granular sludge electrochemical system (AGES) was established by applying the micro-electric field to an aerobic granular sludge (AGS) reactor for the degradation of sulfamethoxazole (SMZ). Under the stimulation of the micro-electric field, the granulation of sludge was improved and the degradation rate of SMZ was enhanced. The features of granular sludge were characterized by scanning electron microscopy and X-ray diffraction. The optimal degradation rate of SMZ (88%) was obtained at the voltage of 3 V and the effective electrode area of 800 mm2. The results of kinetics analyses revealed that the degradation of SMZ by AGES can be fitted with the second-order kinetic equation, showing a degradation rate constant (k) of 0.001 L mol-1·min-1. The degradation products of SMZ in the AGES system were detected by LC-MS and their possible degradation routes were elucidated. The micro-electric field in the AGES system played a selective role in microbes' enrichment and growth, changing the diversity of the microbial community. Pseudomonas, Tolumonas, and Acidovorax were the dominant bacteria in the AGES system, which is accountable for the abatement of SMZ and nutrients. This work provides a green means for improving AGS and paves the way for applying the AGS process to real-world wastewater treatment.

Binding of Dissolved Organic Matter to RNA and Protection from Nuclease-Mediated Degradation.

The persistence of RNA in environmental systems is an important parameter for emerging applications, including ecological surveys, wastewater-based epidemiology, and RNA interference biopesticides. RNA persistence is controlled by its rate of biodegradation, particularly by extracellular enzymes, although the specific factors determining this rate have not been characterized. Due to prior work suggesting that nucleic acids-specifically DNA-interact with dissolved organic matter (DOM), we hypothesized that DOM may bind RNA and impede its biodegradation in natural systems. We first adapted a technique previously used to assess RNA-protein binding to differentiate RNA that is bound at all sites by DOM from RNA that is unbound or partially bound by DOM. Results from this technique suggested that humic acids bound RNA more extensively than fulvic acids. At concentrations of 8-10 mgC/L, humic acids were also found to be more effective than fulvic acids at suppressing enzymatic degradation of RNA. In surface water and soil extract containing DOM, RNA degradation was suppressed by 39-46% relative to pH-adjusted controls. Due to the ability of DOM to both bind and suppress the enzymatic degradation of RNA, RNA biodegradation may be slowed in environmental systems with high DOM concentrations, which may increase its persistence.

Recent developments of mycotoxin-degrading enzymes: identification, preparation and application.

Mycotoxins are secondary metabolites produced by fungi during their growth. They not only seriously affect the yield of food crops but also pose a threat to human and animal health. Physical and chemical methods have been widely used to reduce the production and accumulation of mycotoxins in the field or after harvest, but these methods have difficulty in completely removing mycotoxins while keeping the nutrients at the same time. Biodegradation methods using isolated enzymes have shown superiority and potential for modest reaction conditions, high degradation efficiency and degradation products with low toxicity. Therefore, the occurrence, chemical structures, and toxicology of six prevalent mycotoxins (deoxynivalenol, zearalenone, aflatoxin, patulin, fumonisin, and ochratoxin) were described in this manuscript. The identification and application of mycotoxin-degrading enzymes were thoroughly reviewed. It is believed that in the near future, mycotoxin-degrading enzymes are expected to be commercially developed and used in the feed and food industries.

Three recombinant peroxidases as a degradation agent of aflatoxin M1 applied in milk and beer.

The aim of this work was to estimate the effects of three recombinant peroxidases (rPODs) on the degradation of aflatoxin M1 (AFM1) in a model solution and were applied in milk and beer to study the AFM1 degradation. Besides, the contents of AFM1 in model solution, milk and beer were evaluated, and the kinetic parameters of rPODs were determined (Michaelis-Menten constant - Km and maximal velocity - Vmax). The optimized reaction conditions (The degradation was over 60 %) for these three rPODs in the model solution were, respectively as follows: pH were 9, 9, and 10; hydrogen peroxide concentrations were 60, 50, and 60 mmol/L; at an ionic strength of 75 mmol/L and reaction temperature of 30 °C with 1 mmol/L K+ or 1 mmol/L Na+. These three rPODs (1 U /mL) presented the maximum activity for degradation of AFM1 of 22.4 %, 25.6 %, and 24.3 % in milk, while 14.5 %, 16.9 %, and 18.2 % in beer, respectively. Meanwhile, the survival rate of Hep-G2 cells raised about 1.4 times after treated with peroxidase-generated AFM1 degradation products. Therefore, POD may be a promising alternative to reduce the pollution of AFM1 in model solution, milk, beer, and minimize their impact on the environment in humans.

Treatment Trends and Combined Methods in Removing Pharmaceuticals and Personal Care Products from Wastewater-A Review.

When discharged into wastewater, pharmaceuticals and personal care products (PPCPs) become microorganic contaminants and are among the largest groups of emerging pollutants. Human, animal, and aquatic organisms' exposures to PPCPs have linked them to an array of carcinogenic, mutagenic, and reproductive toxicity risks. For this reason, various methods are being implemented to remove them from water bodies. This report critically reviews these methods and suggests improvements to removal strategies. Biological, physical, and chemical methods such as biological degradation, adsorption, membrane filtration, and advanced electrical and chemical oxidation are the common methods used. However, these processes were not integrated into most studies to take advantage of the different mechanisms specific to each process and are synergistic in the removal of the PPCPs that differ in their physical and chemical characteristics (charge, molecular weight, hydrophobicity, hydrogen bonding, structure). In the review articles published to date, very little information is available on the use of such integrated methods for removing PPCPs. This report attempts to fill this gap with our knowledge.

Prospects for humic acids treatment and recovery in wastewater: A review.

Clean water shortages require the reuse of wastewater. The presence of organic substances such as humic acids in wastewater makes the water treatment process more difficult. Humic acids can significantly affect the removal of heavy metals and other such toxins. Humic acids is formed by the decomposition and transformation of animal and plant remains by microorganisms, and naturally exists in soil and water. It is necessary to degrade and remove humic acids from wastewater. As it seriously human health, effective technologies for removing humic acids from wastewater have attracted great interest over the past decades. This study compared existing techniques for removing humic acids from wastewater, as well as their limitations. Physicochemical treatments including filtration and oxidation are basic and key approaches to removing humic acids. Biological treatments including enzyme and fungi-mediated humic acids degradation are economically feasible but require some scalability. In conclusion, the integrated treatment processes are more significant options for the effective removal of humic acids from wastewater. In addition, humic acids have rich utilization values. It can improve the soil, increase crop yields, and promote the removal of pollutants.

Microbial elimination of carbamate pesticides: specific strains and promising enzymes.

Carbamate pesticides are widely used in the environment, and compared with other pesticides in nature, they are easier to decompose and have less durability. However, due to the improper use of carbamate pesticides, some nontarget organisms still may be harmed. To this end, it is necessary to investigate effective removal or elimination methods for carbamate pesticides. Current effective elimination methods could be divided into four categories: physical removal, chemical reaction, biological degradation, and enzymatic degradation. Physical removal primarily includes elution, adsorption, and supercritical fluid extraction. The chemical reaction includes Fenton oxidation, photo-radiation, and net electron reduction. Biological degradation is an environmental-friendly manner, which achieves degradation by the metabolism of microorganisms. Enzymatic degradation is more promising due to its high substrate specificity and catalytic efficacy. All in all, this review primarily summarizes the property of carbamate pesticides and the traditional degradation methods as well as the promising biological elimination. KEY POINTS: • The occurrence and toxicity of carbamate pesticides were shown. • Biological degradation strains against carbamate pesticides were presented. • Promising enzymes responsible for the degradation of carbamates were discussed.

Structural and functional characterization of an auxiliary domain-containing PET hydrolase from Burkholderiales bacterium.

Biodegradation of polyethylene terephthalate (PET) is one of fundamental ways to solve plastic pollution. As various microbial hydrolases have an extra domain unlike PETase from Ideonella sakaiensis (IsPETase), research on the role of these extra domain in PET hydrolysis is crucial for the identification and selection of a novel PET hydrolase. Here, we report that a PET hydrolase from Burkholderiales bacterium RIFCSPLOWO2_02_FULL_57_36 (BbPETase) with an additional N-terminal domain (BbPETaseAND) shows a similar hydrolysis activity toward microcrystalline PET and a higher thermal stability than IsPETase. Based on detailed structural comparisons between BbPETase and IsPETase, we generated the BbPETaseS335N/T338I/M363I/N365G variant with an enhanced PET-degrading activity and thermal stability. We further revealed that BbPETaseAND contributes to the thermal stability of the enzyme through close contact with the core domain, but the domain might hinder the adhesion of enzyme to PET substrate. We suggest that BbPETase is an enzyme in the evolution of efficient PET degradation and molecular insight into a novel PET hydrolase provides a novel strategy for the development of biodegradation of PET.

Biodegradation of phorate by bacterial strains in the presence of humic acid and metal ions.

Phorate is a systemic insecticide used to eradicate mites, insects, and nematodes. Extensive use of this organophosphate has engendered severe environmental concerns. The current research aimed to explore the kinetic pathways of phorate biodegradation in aqueous solutions. Two novel bacterial strains Pseudomonas aeruginosa strain PR1 (KP268772.1) and Pseudomonas sp. PR_02 (KP268773.1) were isolated, screened, and developed given their potential to degrade phorate. Mineralization of phorate was assayed with and without the addition of metal ions [Fe (II) and Cu (II)] and humic acid (HA). In 14 days, experiment both strains have consumed about 69%-94.5% (half-life from 3.58 to 6.02 days) of phorate. The observed biodegradation rate of phorate with Cu (II) in the system was 73% and 87%, with a half-life of 4.86 and 4.07 days for PR1 and PR2, respectively. The biodegradation of phorate using Fe(II) was 69% and 82%, with half-life periods 5.68 and 4.49 days. Meanwhile, incorporating HA, the phorate biodegradation was inhibited significantly, showing 71% and 85% degradation, with half-life periods of 6.02 and 5.02 days. The results indicated that both bacterial strains were able to mineralize phorate with PR2 > PR1. Summarizing, the inhibition in phorate biodegradation order under different conditions was as HA > Fe (II) > Cu (II). UV-visible measurements and gas chromatography-mass spectrometric assays indicated that the possible degradation pathway of phorate included ethoxy-phosphonothio-methanethiol S-mercaptomethyl-O,O-dihydrogen phosphorodithioate, diethyl-methylphosphonate, methane dithiol, ethanethiol, and phosphate, as the main metabolites identified. Therefore, it was concluded that the newly isolated Pseudomonas strains could be a potential candidates for biodegradation of phorate in a cost-effective, safe, and environmentally friendly alternative.

Biodegradation of 4-chlorophenol in batch and continuous packed bed reactor by isolated Bacillus subtilis.

In present work, biodegradation of 4-Chlorophenol (4-CP) has been successfully achieved using bacteria i.e. Bacillus subtilis (MF447841.1), which was isolated from the wastewater of a nearby drain of Hyundai Motor Company service centre, Agartala, Tripura (India). Geonomic identification was carried out by 16 S rDNA technique and phylogenetic processes. Both, batch and column mode of experiments were performed to optimize various parameters (initial concentration, contact time, dosages etc.) involved in the significant biodegradation of 4-CP. Based on R2 value (0.9789), the Levenspiel's model was found to be best fit than others. The kinetic parameters; specific growth rate (µ), yield of cell mass (YX/S), and saturation constant (KS), were obtained as 0.6383 (h-1), 0.35 (g/g), and 0.006884 (g/L), respectively. The isolated strain has shown the ability of degrading 4-CP up to 1000 mg/L initial concentration within 40 h. Bacterial strain was immobilized via developing calcium alginate beads along by optimizing weight proportion of calcium chloride and sodium alginate and size of the bead for further experiments. Various process parameters i.e. initial feed concentration, bed height, rate of flow of were optimized during packed bed reactor (PBR) study. Maximum biodegradation efficiency of 4-CP was observed as 45.39% at initial concentration of 500 mg/L within 105 min, using 2 mm size of immobilized beads which were formed using 3.5% w/v of both calcium chloride and sodium alginate within. Thus, Bacillus subtilis (MF447841.1) could be used for biological remediation of 4-CP pollutant present in wastewater. Moreover, because of affordable and eco-friendly nature of water treatment, relatively it has the better scope of commercialization.

Exceptionally rich keratinolytic enzyme profile found in the rare actinomycetes Amycolatopsis keratiniphila D2T.

The non-spore forming Gram-positive actinomycetes Amycolatopsis keratiniphila subsp. keratiniphila D2T (DSM 44,409) has a high potential for keratin valorization as demonstrated by a novel biotechnological microbial conversion process consisting of a bacterial growth phase and a keratinolytic phase, respectively. Compared to the most gifted keratinolytic Bacillus species, a very large number of 621 putative proteases are encoded by the genome of Amycolatopsis keratiniphila subsp. keratiniphila D2T, as predicted by using Peptide Pattern Recognition (PPR) analysis. Proteome analysis by using LC-MS/MS on aliquots of the supernatant of A. keratiniphila subsp. keratiniphila D2T culture on slaughterhouse pig bristle meal, removed at 24, 48, 96 and 120 h of growth, identified 43 proteases. This was supplemented by proteome analysis of specific fractions after enrichment of the supernatant by anion exchange chromatography leading to identification of 50 proteases. Overall 57 different proteases were identified corresponding to 30% of the 186 proteins identified from the culture supernatant and distributed as 17 metalloproteases from 11 families, including an M36 protease, 38 serine proteases from 4 families, and 13 proteolytic enzymes from other families. Notably, M36 keratinolytic proteases are prominent in fungi, but seem not to have been discovered in bacteria previously. Two S01 family peptidases, named T- and C-like proteases, prominent in the culture supernatant, were purified and shown to possess a high azo-keratin/azo-casein hydrolytic activity ratio. The C-like protease revealed excellent thermostability, giving promise for successful applications in biorefinery processes. Notably, the bacterium seems not to secrete enzymes for cleavage of disulfides in the keratinous substrates. KEY POINTS: • A. keratiniphila subsp. keratiniphila D2T is predicted to encode 621 proteases. • This actinomycete efficiently converts bristle meal to a protein hydrolysate. • Proteome analysis identified 57 proteases in its secretome.

Comparative Study of the Biological Degradation of Poly(3-Hydroxybutyrate-co-3-Hydroxyhexanoate) Microbeads in Municipal Wastewater in Environmental and Controlled Laboratory Conditions.

From April to June 2019, poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (P3(HA)) microbead samples were exposed to an operational wastewater reclamation facility (WWRF) in an aerobic aeration basin in Athens, Georgia. Samples were withdrawn from the facility over a 13-week timeframe, and the particles were examined by Raman microscopy and thermogravimetric analysis/mass spectroscopy (TGA/MS) coupled with differential scanning calorimetry (DSC). The activated sludge from this facility was also used as an inoculum to examine carbon mineralization under controlled respirometry experiments to corroborate biological degradation rates determined from both the environmental and laboratory approach. Respirometry, Raman microscopy, and TGA/MS-DSC methods all measured similar biodegradation timelines for microbeads bound to an epoxy substrate, indicating that the three methods are temporally comparable and may be used to measure material biological degradation. Samples of epoxy-bound P3(HA) microbeads, free microbeads, the P3(HA) film, and poly(lactic acid) (PLA) film demonstrated carbon mineralization of 90.0, 89.4, 95.0, and 8.15%, respectively, relative to the cellulose positive control. Using a modified Gompertz growth model, the biological degradation rate coefficients (Rm) were determined for cellulose, P3(HA) film, epoxy-bound P3(HA) microbeads, and free P3(HA) microbeads and found to be 31.6, 30.2, 17.5, and 18.7 mL CO2·g-1·day-1, respectively. Moreover, P3(HA) microbeads can efficiently mineralize in WWRF infrastructure at a rate comparable to cellulose.

Detection and removal of poly and perfluoroalkyl polluting substances for sustainable environment.

PFAs (poly and perfluoroalkyl compounds) are hazardous and bioaccumulative chemicals that do not readily biodegrade or neutralize under normal environmental conditions. They have various industrial, commercial, domestic and defence applications. According to the Organization for Economic Co-operation and Development, there are around 4700 PFAs registered to date. They are present in every stream of life, and they are often emerging and are even difficult to be detected by the standard chemical methods. This review aims to focus on the sources of various PFAs and the toxicities they impose on the environment and especially on humankind. Drinking water, food packaging, industrial areas and commercial household products are the primary PFAs sources. Some of the well-known treatment methods for remediation of PFAs presented in the literature are activated carbon, filtration, reverse osmosis, nano filtration, oxidation processes etc. The crucial stage of handling the PFAs occurs in determining and analysing the type of PFA and its remedy. This paper provides a state-of-the-art review of determination & tools, and techniques for remediation of PFAs in the environment. Improving new treatment methodologies that are economical and sustainable are essential for excluding the PFAs from the environment.

Bioremediation of polycyclic aromatic hydrocarbons in contaminated mangroves: Understanding the historical and key parameter profiles.

Sensitive biomes, such as coastal ecosystems, have become increasingly susceptible to environmental impacts caused by oil logistics and storing, which, although more efficient nowadays, still cause spills. Thus, bioremediation techniques attract attention owing to their low impact on the environment. Among petroleum-based compounds, polycyclic aromatic hydrocarbons (PAHs) are known for their potential impact and persistence in the environment. Therefore, PAH bioremediation is notably a technique capable of reducing these polluting compounds in the environment. However, there is a lack of understanding of microbial growth process conditions, leading to a less efficient choice of bioremediation methods. This article provides a review of the bioremediation processes in mangroves contaminated with oils and PAHs and an overview of some physicochemical and biological factors. Special attention was given to the lack of approach regarding experiments that have been conducted in situ and that considered the predominance of the anaerobic condition of mangroves.

Enhanced Sinks of Polycyclic Aromatic Hydrocarbons Due to Kuroshio Intrusion: Implications on Biogeochemical Processes in the Ocean-Dominated Marginal Seas.

The biogeochemical processes of polycyclic aromatic hydrocarbons (PAHs) in the South China Sea (SCS) are influenced by the exchanges of water masses, energies, and materials between this marginal sea and the Pacific Ocean. To investigate the impact of oceanic water intrusion on semivolatile compounds, we collected seawater samples in the Western Pacific, northern, and central SCS in 2017 and analyzed for dissolved PAHs. PAH concentrations in the water columns of the Pacific Ocean and SCS were 1.7-11 and 1.1-7.3 ng L-1, respectively, showing spatial distinctions in terms of the composition and source characteristics. A common depletion for three-ring PAHs was found in the northern SCS by comparing the modeling results of conservative mixing by Kuroshio intrusion. Kuroshio water increased the levels of temperature, dissolved oxygen, and nutrients when intruding into the northern SCS and was likely to enhance the bioavailability of PAHs and stimulate their biodegradation process. In the water column, the most effective layer under the Kuroshio intrusion impact is different for three- and four-ring PAHs, where the three-ring PAHs' depletion was most significant at the surface; however, for four-ring PAHs, that was at the deep chlorophyll maximum layer. This study highlighted the effect of ocean currents on PAHs for their water-column processes both from physical and biogeochemical perspectives.

Advances in researches of the mulch-film degradation and the underlying mechanism.

Mulch-filmaccounted for more than half of plastic film used in Chinese agriculture. The wide utilization of mulch-film brings great economic value but also causes "white pollution". The residual film is difficult to be recycled and degraded, which directly affects soil regeneration. We introduced the current status of the plastic film usage in China and reviwed the research progress in its degradation. The biological and non-biological pathways and mechanisms of mulch-film degradation were summarized, with particular focus on the polyolefin degradation with synergistic effect of photocatalysis, metal ion doping as well as the impacts of different sources of bacteria and enzymes on the degradation efficiency of polyolefins. The more efficient degradation methods of plastic film are prospected. This review would provide reference for the further studies of plastic film degradation and microplastic degradation.

Isolation and characterization of a Pseudomonas poae JSU-Y1 with patulin degradation ability and biocontrol potential against Penicillium expansum.

Patulin, one of the most common mycotoxins produced primarily by the Penicillium, Aspergillus and Byssochlamys species, is often associated with fruits and fruit-based products. Biodegradation by microbes is an effective method to remove or detoxify mycotoxins. In this study, a bacterial strain with patulin degradation capability was selectively isolated using oxindole, an analogue to patulin, as the sole carbon source, and identified as Pseudomonas poae JSU-Y1 by phylogenetic analysis on the basis of 16S rRNA sequence. This isolated bacterium could inhibit the growth of Penicillium expansum both on plate medium and apple fruit with inhibition ratio of 30.3% and 44.9%, respectively. Up to 87.7% of the initial patulin (2.5 µg/mL) was removed after incubation with Pseudomonas poae JSU-Y1 in liquid medium at 30 °C for 72 h. When challenged with apple juice, 79% of patulin could be degraded by this isolated strain. Additionally, ascladiol was tentatively identified as the patulin degradation intermediate by LC-MS analysis. Taken together, the experiment results indicated that the isolated Pseudomonas poae JSU-Y1 would be a promising bacterial resource to control patulin contamination and toxigenic fungal growth in agricultural products.

Deoxynivalenol: Masked forms, fate during food processing, and potential biological remedies.

Deoxynivalenol (DON) has drawn global attention because of its prevalence and significant effects on human or animal health. Biological remedies for DON have been developed from preharvest to postharvest. Applying microbes, including bacteria, fungi (yeast and molds), and enzymes, results in inhibited synthesis, structural destruction, or adsorption of DON. DON can be degraded into masked forms by phase I metabolism or phase II metabolism. During food processing, DON content changes dynamically and is even transformed. Physical, chemical, thermal, or biological processes physically reduce DON content. Temperature, heating time, enzymes, food additives, microorganisms, food composition, contamination level, and other ingredients are key factors. Although DON content can be reduced during food processing, increases in other toxins, such as DON-3-ß-d-glucoside and 3-acetyl-DON, can be potentially risky. The application of biodegradation methods in food processing bears research significance. Both microorganisms and enzymes can be potentially used. Novel techniques, such as RNA interference, omics technologies, or enzymes coupled with the genetic engineering method, can be introduced. This review systematically updates the understanding of masked forms of DON, biological degradation strategy, fate of DON during processing, and future trends for biodegradation. Challenges to the successful application of biological methods may include the stability and suitability of the detoxification agents, security of degradation products, and successful application for industrial production.