Biodegradation Of Phenol Research Articles

Identification and isolation of efficient phenol-degrading and heavy metal-resistant bacteria from seasonal catchments of the Lut Desert

ABSTRACT The present study was conducted to isolate and identify a phenol-degrading bacterial strain resistant to cadmium obtained from seasonal catchments of the Lut Desert, Iran. Additionally, optimal conditions affecting biological phenol degradation, including pH, temperature, salinity, and carbon-to-nitrogen ratio, were determined using the Taguchi method, and the ability of the purified strain to degrade phenol in different concentrations was investigated. Isolated bacterium strain Bacillus cereus LD-1, capable of phenol degradation and cadmium tolerance, could tolerate and degrade phenol up to a concentration of 1,500 mg/L. All optimized factors except carbon-to-nitrogen ratio had a significant effect on the rate of phenol biodegradation. Among the selected factors, based on the effect size, pH had the highest impact (10.02), followed by salinity (6.16), temperature (5.61), and C:N ratio (2.55) on phenol biodegradation. The optimal conditions for phenol biodegradation were determined as pH of 8, temperature of 30 °C, salinity of 0 g/L, and C:N ratio of 100:30. Under optimal conditions, 80.57% of phenol was decomposed by the LD-1 strain. Considering the high ability of the isolated strain for phenol degradation in the presence of 100 mg/L cadmium, LD-1 can be applied in the biological treatment of phenolic effluents contaminated with heavy metals.

Assistance of aminated straw on enhanced biodegradation of phenol through bacteria and potential prediction of machine learning for bioremediation

ABSTRACT How to treat phenol-containing wastewater harmlessly is an urgent problem to be solved. In this study, a kind of biomaterial was prepared through strain PAO1 immobilized on aminated straw to enhance the phenol removal rate and efficiency. The aminated straw assisted PAO1 to increase the phenol degraded concentration from 1,900 to 1,500 mg/L, and shorten the degraded time by 44 h at 1,500 mg/L phenol. The immobilized PAO1 could remove phenol at pH 10 and 11, which was 2.7 and 3.8 times higher than free bacteria, respectively. In addition, the immobilized PAO1 could totally remove phenol, which was twice as high as that of free bacteria, at 4% NaCl stress. Furthermore, the removal efficiency of immobilized PAO1 was higher than that of free bacteria under the stress of various metal ions, especially for Co2+ and Pb2+. The determination coefficients R2 and root mean square error showed that the back propagation artificial neural network model could predict the degradation of phenol under various conditions, saving time and economic cost. The present study envisions that this biomaterial has great potential in the bioremediation of organic pollutions.

Aerobic phenol degradation using native bacterial consortium via ortho-and meta-cleavage pathways.

Effective bioremediation of a phenol-polluted environment harnesses microorganisms' ability to utilize hazardous compounds as beneficial degraders. In the present study, a consortium consisting of 15 bacterial strains was utilized. The current study aims to monitor the phenol biodegradation pathway. The tested consortium showed effective potential in the bioremediation of phenol-contaminated industrial wastewater. The enzymatic studies conducted brought to light that the bacterial consortium under test was proficient in degrading phenol under aerobic conditions while exhibiting the simultaneous expression of both ortho- and meta-cleavage pathways. It was observed that pheA, pheB, and C12O genes were maximally expressed, and the enzymes responsible for phenol degradation, namely, phenol hydroxylase, catechol 1,2-dioxygenase, and catechol 2,3-dioxygenase, reached maximum activity after 48 h of incubation with a 20-ppm phenol concentration. To gain a deeper understanding of the activation of both ortho- and meta-cleavage pathways involved in phenol degradation, a technique known as differential display reverse transcriptase polymerase chain reaction (DDRT-PCR) was applied. This method allowed for the specific amplification and detection of genes responsible for phenol degradation. The expression levels of these genes determined the extent to which both ortho- and meta-cleavage pathways were activated in response to the presence of phenol.

The dual role of biochar in boosting phenol biodegradation and anti-inhibition performance against hazardous substrate

Enhancing the biodegradation of hazardous recalcitrant organic compounds from wastewater has garnered increasing attention. Herein, bamboo biochar was screened for subsequent investigation as it considerably enhanced hazardous phenol removal efficiency by 125.68 % over the biochar-free system at 700 mg/L. Besides, the influencing factors were optimized, including biochar dosage and phenol concentration. However, the phenol removal rate decreased by 75.91 % within 15 hours when utilizing biochar oxidized by H2O2, perhaps due to eliminating aromatic clusters on biochar. Combined with FTIR analysis, CO and -OH on aromatic clusters of biochar were recognized as the underlying contributors to facilitating electron transfer in phenol biodegradation. Furthermore, the ortho-disubstituted benzene ring was discovered on biochar, which may originate from catechol, an intermediate during phenol degradation, suggesting that biochar also serves as a site for phenol biodegradation. Moreover, the fabricated biochar-sodium alginate microspheres enhanced anti-inhibition to phenol over suspended bacteria by 192.15 %. The system also eliminated 99.93 % of phenol after the seven recycles at 1258.75 mg/L, exhibiting excellent reusability. This work provides valuable insights into bioaugmentation strategies for bio-degrading phenol using biochar.

Phenol Biodegradation by Three Bacterial Strains Stimulated by Constant Electric Field

Objective: The aim of the present study is to compare phenol biodegradation activity of bacteria from the strains Xanthobacter autotrophicus GJ 10, Pseudomonas denitrificans and Pseudomonas putida enhanced by constant electric field in a potentiostatic mode by free cultures and immobilized cells on granulated activated carbon. Theoretical Framework: The work is based on the concept of biodegradation in constant electric field due to the enhanced removal of intermediate inhibitors produced from phenol. These intermediate may affect slightly microbial growth but the biodegradation capacity is enhanced. Method: The methodology adopted for this research comprises bioelectrochemical oxidative microbial biodegradation of phenol at constant anode potential. Results and Discussion: The obtained results revealed the positive effect of the electric field on the phenol biodegradation rate for all of the considered strains. There is certain anode potential at which the biodegradation rate is strongly affected for each strain. Research Implications: The research have both practical and theoretical implications. The practical importance consists in the enhanced biodegradation of severe pollutant as phenol is. The theoretical importance is within the specific impact of constant electric field on the enzyme activities in the studied strains. Originality/Value: This study contributes to the literature by the innovative approach and the practical aspects. The relevance and value of this research are demosntated by enhancement of phenol biodegradation in wastewater and water ponds.

Collaboration of bacterial consortia for biodegradation of high concentration phenol and potential application of machine learning

Mixed culture of microorganisms is an effective method to remove high concentration of phenol in wastewater. At present, it is still a challenge for microorganisms to remove high-concentration phenol from wastewater. In this study, a phenol-degrading consortium was isolated, which could rapidly degrade 1800 mg/L phenol within 30 h, and the highest phenol degradation concentration was 2000 mg/L. Further exploration of how microbial consortium cooperates to promote phenol biodegradation was studied: the core bacteria of the microbial consortium was relatively stable during phenol degradation; the bacteria could improve the adaptability to environment and metabolic ability of phenol, by producing more surfactants and betaine, thereby improving the degradation rate. The determination coefficient (R2) in the machine learning model showed that the back propagation artificial neural network (BP-ANN) can predict the biodegradation of phenol under different conditions, saving time and economic costs. This study explains how microbial consortium cooperates to degrade phenol from the aspects of microbial consortium composition and metabolic analysis, which provides a theoretical basis for mixed culture microorganisms to degrade pollutants.

Determination of the amount of oxygen required for each function in the bacterial cell during phenol biodegradation in wastewater: a unique concept

The goal of this study is to provide more in-depth study into the biodegradation of phenol and to determine the amount of oxygen required for each function in the bacterial cell which is fundamental in understanding of cell metabolism and biology. The total amount of oxygen consumed by bacteria is determined using manometric technique. In the biodegradation of phenol (less than 150 mg/L) the oxygen consumed up to the plateau (the stage associated with the termination of carbon) is found to be composed of three portions, one is used to directly oxidize portion of the substrate to produce energy to allow normal cell functions to sustain life which is estimated to be 50% of the plateau BOD (biochemical oxygen demand), the second portion is to oxidize energy storage intermediate (most probably carbon mono oxide, CO, is oxidized to CO2) to release energy which is then used to power reproduction which is estimated to be 41.75% of the plateau BOD, third portion is incorporated into the produced new cells which is estimated to be 8.25% of the plateau BOD. The correlation coefficient between the initial phenol concentration and the ultimate BOD values is found to be r = 0.9999. This value of correlation coefficient, r, may indicate that microbes are, in a way, estimating the amount of food available and they grow and reproduce accordingly. This article provides a better understanding of cell metabolism and biology. This understanding of cell metabolism may offer better understanding of human cells. The results of this research paves the way for a similar research on human cells where abnormal oxygen uptake may assist in early prediction of cells dysfunction and diseases and may help in early taking the necessary precautions to avoid illness.

A novel paraffin-based N/P controlled-release material for biostimulation of phenol biodegradation in groundwater

To address the problem of the weak natural restoration ability of oligotrophic groundwater environments, a novel N/P controlled-release material (CRM) for biostimulation, prepared by an improved method, was developed. CRMs can encapsulate N and P (N/P) salts for sustained release in aquifers. Paraffin-based CRMs can be used to control N/P release rates by adjusting the particle size of CRMs and the mass ratio of the paraffin. The developed CRMs had a more remarkable adaptability to groundwater than other materials. Specifically, 0.4-cm CRMs released N/P stably and efficiently over a wide temperature range (7–25 ℃), and the release properties of various CRMs were not affected by pH. The release of N/P followed Fickian diffusion, and a dissolution-diffusion model was established to elucidate the mechanism of the controlled release. In contrast to bare N/P, CRMs obviously enhanced the biodegradation rate of phenol and prolonged the effectiveness of supplying N/P. The degradation rate of phenol in the CRM system increased by 20.8 %. The different supply modes of N/P, CRMs and bare N/P, resulted in differences in salinity. Metagenomic analysis showed that this difference changed the proportion of various phenol-degrading genera and thus changed the abundance of genes associated with the phenol degradation pathway.

Taxonomic identification, phenol biodegradation and soil remediation of the strain Rhodococcus sacchari sp. nov. Z13T.

Phenols are highly toxic chemicals that are extensively used in industry and produce large amounts of emissions. Notably, phenols released into the soil are highly persistent, causing long-term harm to human health and the environment. In this study, a gram-positive, aerobic, and rod-shaped bacterial strain, Z13T, with efficient phenol degradation ability, was isolated from the soil of sugarcane fields. Based on the physiological properties and genomic features, strain Z13T is considered as a novel species of the genus Rhodococcus, for which the name Rhodococcus sacchari sp. nov. is proposed. The type strain is Z13T (= CCTCC AB 2022327T = JCM 35797T). This strain can use phenol as its sole carbon source. Z13T was able to completely degrade 1200mg/L phenol within 20h; the maximum specific growth rate was μmax = 0.93174h-1, and the maximum specific degradation rate was qmax = 0.47405h-1. Based on whole-genome sequencing and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis, strain Z13T contains a series of phenol degradation genes, including dmpP, CatA, dmpB, pcaG, and pcaH, and can metabolize aromatic compounds. Moreover, the potential of strain Z13T for soil remediation was investigated by introducing Z13T into simulated phenol-contaminated soil, and the soil microbial diversity was analyzed. The results showed that 100% of the phenol in the soil was removed within 7.5 d. Furthermore, microbial diversity analysis revealed an increase in the relative species richness of Oceanobacillus, Chungangia, and Bacillus.

Symbiotic virus-bacteria interactions in biological treatment of coking wastewater manipulating bacterial physiological activities

Biological treatment is commonly used in coking wastewater (CWW) treatment. Prokaryotic microbial communities in CWW treatment have been comprehensively studied. However, viruses, as the critical microorganisms affecting microbial processes and thus engineering parameters, still remain poorly understood in CWW treatment context. Employing viromics sequencing, the composition and function of the viral community in CWW treatment were discovered, revealing novel viral communities and key auxiliary metabolic functions. Caudovirales appeared to be the predominant viral order in the oxic-hydrolytic-oxic (OHO) CWW treatment combination, showing relative abundances of 62.47 %, 56.64 % and 92.20 % in bioreactors O1, H and O2, respectively. At the family level, Myoviridae, Podoviridae and Siphoviridae mainly prevailed in bioreactors O1 and H while Phycodnaviridae dominated in O2. A total of 56.23–92.24% of novel viral contigs defied family-level characterization in this distinct CWW habitat. The virus-host prediction results revealed most viruses infecting the specific functional taxa Pseudomonas, Acidovorax and Thauera in the entire OHO combination, demonstrating the viruses affecting bacterial physiology and pollutants removal from CWW. Viral auxiliary metabolic genes (AMGs) were screened, revealing their involvement in the metabolism of contaminants and toxicity tolerance. In the bioreactor O1, AMGs were enriched in detoxification and phosphorus ingestion, where glutathione S-transferase (GSTs) and beta-ketoadipyl CoA thiolase (fadA) participated in biodegradation of polycyclic aromatic hydrocarbons and phenols, respectively. In the bioreactors H and O2, the AMGs focused on cell division and epicyte formation of the hosts, where GDPmannose 4,6-dehydratase (gmd) related to lipopolysaccharides biosynthesis was considered to play an important role in the growth of nitrifiers. The diversities of viruses and AMGs decreased along the CWW treatment process, pointing to a reinforced virus-host adaptive strategy in stressful operation environments. In this study, the symbiotic virus-bacteria interaction patterns were proposed with a theoretical basis for promoting CWW biological treatment efficiency. The findings filled the gaps in the virus-bacteria interactions at the full-scale CWW treatment and provided great value for understanding the mechanism of biological toxicity and sludge activity in industrial wastewater treatment.

Recent developments in moving bed biofilm reactor (MBBR) for the treatment of phenolic wastewater -A review

BackgroundPhenol, a toxic and carcinogenic compound found in industrial effluent, poses a severe threat to the environment and aquatic life. Conventional methods such as physio-chemical techniques have limitations in efficiency, cost, and sustainability, leading to the development of advanced hybrid approaches like the Moving Bed Biofilm Reactor (MBBR) to treat phenols. Review methodIn this study, we aimed at an in-depth review of MBBR for the remediation of phenolic wastewater at an industrial scale. The review uses a methodology that involves a comparative analysis of various conventional methods, including activated sludge process (ASP), sequencing batch biofilm reactor (SBBR), Fluidized Bed Biofilm Rector (FBBR), and trickling filter (TF) with MBBR, to determine their efficacy in phenol degradation. In this context, a thorough bibliometric assay of MBBR is carried out to understand the recent publication trends. The study also examines the impact of different types and shapes of bio-carriers and their filling ratios on phenol biodegradation. Significant findingThe present work demonstrates the feasibility of using an aerobic MBBR along with a Fenton-like system (advanced oxidation processes) to treat phenolic effluent LCCA is discussed for selected treatment methods for assessing the sustainability aspects. In light of recent advancements, future research endeavors should prioritize the refinement and optimization of MBBR systems to strengthen their efficiency and sustainability, thus paving the way for a greener and cleaner future.

Enhanced biodegradation of phenol under Cr(VI) stress by microbial collaboration and potential application of machine learning for phenol biodegradation.

Cr(VI) and phenol commonly coexist in wastewater, posing a great threat to the environment and human health. However, it is still a challenge for microorganisms to degrade phenol under high Cr(VI) stress. In this study, the phenol-degrading strain Bacillus cereus ZWB3 was co-cultured with the Cr(VI)-reducing strain Bacillus licheniformis MZ-1 to enhance phenol biodegradation under Cr(Ⅵ) stress. Compared with phenol-degrading strain ZWB3, which has weak tolerance to Cr(Ⅵ), and Cr(Ⅵ)-reducing strain MZ-1, which has no phenol-degrading ability, the co-culture of two strains could significantly increase the degraded rate and capacity of phenol. In addition, the co-cultured strains exhibited phenol degradation ability over a wide pH range (7-10). The reduced content of intracellular proteins and polysaccharides produced by the co-cultured strains contributed to the enhancement of phenol degradation and Cr(Ⅵ) tolerance. The determination coefficients R2, RMSE, and MAPE showed that the BP-ANN model could predict the degradation of phenol under various conditions, which saved time and economic cost. The metabolic pathway of microbial degradation of phenol was deduced by metabolic analysis. This study provides a valuable strategy for wastewater treatment containing Cr(Ⅵ) and phenol.

An effective strategy for biodegradation of high concentration phenol in soil via biochar-immobilized Rhodococcus pyridinivorans B403.

High concentration of phenol residues in soil are harmful to human health and ecological safety. However, limited information is available on the in-situ bioremediation of phenol-contaminated soil using biochar as a carrier for bacteria. In this study, bamboo -derived biochar was screened as a carrier to assemble microorganism-immobilized composite with Rhodococcus pyridinivorans B403. Then, SEM used to observe the micromorphology of composite and its bioactivity was detected in solution and soil. Finally, we investigated the effects of free B403 and biochar-immobilized B403 (BCJ) on phenol biodegradation in two types of soils and different initial phenol concentrations. Findings showed that bacterial cells were intensively distributed in/onto the carriers, showing high survival. Immobilisation increased the phenol degradation rate of strain B403 by 1.45 times (37.7mg/(L·h)). The phenol removed by BCJ in soil was 81% higher than free B403 on the first day. Moreover, the removal of BCJ remained above 51% even at phenol concentration of 1,500mg/kg, while it was only 15% for free B403. Compared with the other treatment groups, BCJ showed the best phenol removal effect in both tested soils. Our results indicate that the biochar-B403 composite has great potential in the remediation of high phenol-contaminated soil.

Bioremediation of phenolic compounds in coal‐contaminated environments: Bio‐kinetic studies using a mixed bacterial culture

AbstractTwo distinct bacterial strains were combined in a mixed culture to investigate the degradation of phenol. The mixed cultures consisting of species like Rhodococcus and Bacillus, were isolated from the waste effluent collected from Dankuni coal complex (DCC) in West Bengal. The experimental phenol biodegradation were performed batch wise at an optimized temperature and pH conditions of 37°C and 7.0 for a wide range of phenol concentrations initially, with saline solutions which is not supplemented with nutrients initially. Experimental results concluded a highest possible specific growth rate at 150 mg/L for phenol biodegradation of 2400 mg/L within a span of 72 h. Several significant physicochemical parameters were investigated in order to determine the ideal conditions for phenol breakdown. It was also observed that a spectroscopic study of the intermediate at 260 nm of the phenol biodegradation commenced through the formation of a cis, cis intermediate, indicating ortho‐cleavage pathway. A simulated substrate utilization and growth profiles was obtained by using substrate inhibition model equation using MATLAB R2017a were used to compare for the validation of the obtained experimental growth and substrate characterization data.

Isolation and Characterization of Yarrowia lipolytica YQ22 from Diesel Samples for Phenol Biodegradation

Phenolic compounds have gained international interest due to their carcinogenic, toxic, and bioaccumulative properties, causing adverse effects in both animals and humans. As a result, there is a growing interest in finding alternative and eco-friendly treatment routes for phenol by exploring new microbial cultures with potential adaptation and biodegradation capabilities. In this study, the phenol removal efficiency of Yarrowia lipolytica YQ22 under laboratory conditions was determined. The YQ22 strain was obtained from diesel samples from a fuel station in Trujillo, Peru, isolated through serial dilutions on Sabouraud agar, and identified through its morphological characteristics using microscopy and molecular analysis by polymerase chain reaction of the ribosomal DNA internal transcribed spacer (ITS) and 5.8S regions. In the treatment, the effect of pH (5, 6 and 7) and temperature (25°C, 30°C and 35°C) on phenol removal with 2% (v/v) inoculum of Yarrowia lipolytica from 48-hour growth was evaluated. Phenol concentration was measured by high-performance liquid chromatography. A maximum phenol removal percentage of 61.18 was obtained for YQ22 at 30°C, pH 5 and 120 rpm during 48 hours. These findings demonstrate the ability of Yarrowia lipolytica to remove phenol and suggest its potential use in the field of bioremediation of phenolic compounds and their derivatives.

Continuous Phenol Biodegradation in a Bioreactor at Upflow Packed Bed by Mixed Microbial Culture

Continuous Phenol Biodegradation in a Bioreactor at Upflow Packed Bed by Mixed Microbial Culture

Phenol biodegradation using bio-filter tower packed column with immobilized bacterial consortium: a batch test study.

The effluents from pulp and paper manufacturing industries contain high concentrations of phenol, which when discharged directly into surface water streams, increases the biological oxygen demand (BOD) and chemical oxygen demand (COD). In this study, two dominant bacteria SP-4 and SP-8 were isolated from the effluent emanating with a pulp and paper industry. The selected phenol-degrading isolates were identified as Staphylococcus sp. and Staphylococcus sciuri respectively by using nucleotide sequence alignment and phylogenetic analysis of 16S rRNA regions of the genome. The two isolates used for the biodegradation process effectively degraded phenol concentration of pulp and paper industry effluent upto 1600 and 1800mg/L resepctively. The individual isolates and consortium were immobilized using activated carbon, wood dust, and coal ash. Additionally, the effluent was treated using a bio-filter tower packed column immobilized with bacterial cells at a constant flow rate of 5 mL/min. The present study showed that the developed immobilized microbial consortium can effectively degrade 99% of the phenol present in pulp and paper industry effluents, resulting in a significant reduction in BOD and COD of the system. This study can be well implemented on real-scale systems as the bio-filter towers packed with immobilized bacterial consortium can effectively treat phenol concentrations up to 1800mg/L. The study can be implemented for bioremediation processes in phenolic wastewater-contaminated sites.

Removal of Phenol by Rhodococcus opacus 1CP after Dormancy: Insight into Enzymes' Induction, Specificity, and Cells Viability.

Biodegradation of phenol is an effective method for removing this toxicant from contaminated sites. Phenol is a toxic compound for living cells, so many bacteria degrade phenol in relatively low concentrations, up to 0.75 g L-1. The Rhodococcus opacus strain 1CP is an effective destructor of a wide range of pollutants. In the absence of a carbon source in the medium, cells of the R. opacus 1CP strain easily form cyst-like resting cells (CLC). The purpose of this work was to evaluate the viability of cells during long-term storage and the efficiency of the process of phenol destruction by R. opacus 1CP cells germinating after dormancy. Resting cells were obtained by simple cultivation in a rich medium followed by storage under static conditions. This is a simple approach to obtain a large amount of biomass. Decomposition of phenol proceeded via catechol followed by ortho-cleavage of aromatic ring. The induction of three phenol hydroxylases was detected by RT-PCR in cells germinated in a mineral medium with phenol as the carbon source. The stability of the genome of cells germinating after dormancy is shown by box-PCR. Dormant R. opacus 1CP cells, both suspended and immobilized, can be directly used for the decomposition of phenol after 4-12 months storage. In addition to phenol, after 9 months of storage, immobilized germinating cells easily metabolized 4-chlorophenol and 2,4,6-trichlorophenol. The results demonstrate a potential and simple approach toward achieving long-term storage of cells for further use in bioremediation.

The potential of Stenotrophomonas maltophilia KB2 for 1 phenol degradation 2 under exposure to heavy metal

The large diversity of chemical substances present in air, water, or soil makes it necessary tostudy their mutual impact on the effectiveness of microbiological decomposition ofcontaminants. This publication presents the results of the studies aimed at evaluating the effect of two biogenic heavy metals - zinc and copper - on the phenol biodegradation by the Stenotrophomonas maltophilia KB2 strain. The tests were carried out for concentrations ofmetals significantly exceeding the legally permitted wastewater values: for zinc up to13.3 g·m -3, and copper up to 3.33 g·m -3. In the tested metal concentration range, phenol biodegradation by the S. maltophilia KB2 strain was not significantly influenced by theintroduced dose of zinc. While the presence of copper inhibited both biomass growth andsubstrate degradation. Kinetic data of metal and phenol mixtures were analyzed and very goodcorrelations were obtained for the proposed equations. An equation consistents with the Hanand Levenspiel model was proposed for the system S. maltophilia KB2-phenol-copper, whilean equation consistents with the Kai model for the system St. maltophilia KB2-phenol-zinc. The simultaneous presence of Zn and Cu ions in the culture resulted in a stronger inhibition ofphenol biodegradation.

Phenolic compounds induce ferroptosis-like death by promoting hydroxyl radical generation in the Fenton reaction

Phenolic compounds are industrially versatile chemicals, also the most ubiquitous pollutants. Recently, biosynthesis and biodegradation of phenols has attracted increasing attention, while phenols’ toxicity is a major issue. Here, we evolved phloroglucinol-tolerant Escherichia coli strains via adaptive evolution, and three mutations (ΔsodB, ΔclpX and fetAB overexpression) prove of great assistance in the tolerance improvement. We discover that phloroglucinol complexes with iron and promotes the generation of hydroxyl radicals in Fenton reaction, which leads to reducing power depletion, lipid peroxidation, and ferroptosis-like cell death of E. coli. Besides phloroglucinol, various phenols can trigger ferroptosis-like death in diverse organisms, from bacteria to mammalian cells. Furthermore, repressing this ferroptosis-like death improves phloroglucinol production and phenol degradation by corresponding strains respectively, showing great application potential in microbial degradation or production of desired phenolic compounds, and phloroglucinol-induced ferroptosis suppresses tumor growth in mice, indicating phloroglucinol as a promising drug for cancer treatment.