Cited by 58Microbial bioremediation and biosurfactantsEnvironmental remediation with nanomaterialsMicrobial Fuel Cells and Bioremediation

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

A critical review of recent advances in the bio-remediation of chlorinated substances by microbial dechlorinators

Open access
Dutta, Nalok, Usman, Muhammad, Ashraf, Muhammad Awais, Luo, Gang, Zhang, Shicheng·2022·Chemical Engineering Journal Advances

Abstract

A significant health risk is associated with chlorinated hydrocarbon contamination in soils and groundwater. Microbial reductive dechlorination, one of the major pathways of chlorinated hydrocarbon degradation, has been extensively studied in anaerobic subsurface environments. The current study presents a comprehensive review and advancement related to the enhanced in-situ reductive dechlorination of chloroethenes, polychlorinated biphenyls, and chloroethenes in the recent past. Reductive dechlorination is an important pathway for dechlorination in an anaerobic environment performed by a wide group of fermentative, methanogenic, iron, and sulfate-reducing microbial populations for complete degradation of chloroethenes. Presently, the most widely used biotic remediation technologies are based on functional anaerobic bacteria. Although this technology can be used in treating hazardous contaminants yet, the problem surfaces when natural electron acceptors such as nitrates, sulphates, and bicarbonates compete with the target contaminants for electrons. Therefore, in order to accurately evaluate the effectiveness of this technology under natural hydro-chemical conditions, a thorough mechanistic overview of electron competition and electron selectivity is critical to understanding the mechanisms governing these phenomena. This review aims to provide an overview of functional microbes in eliciting in-situ biostimulation or bioaugmentation strategies that can be implemented in future research studies pertaining to this domain.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1016/j.ceja.2022.100359

Cites

1 of 1 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Microbial processes are crucial in decomposing organic pollutants, utilizing various catalytic mechanisms to break down complex chemicals into simpler, safer components.

    “Microbial processes are crucial in decomposing organic pollutants, utilizing various catalytic mechanisms to break down complex chemicals into simpler, safer components [99].”

    From Harnessing bacterial consortia for effective bioremediation: targeted removal of heavy metals, hydrocarbons, and persistent pollutants (2025) · cites this paper as [99]

    Section 2, “Microbially mediated dechlorination process” (page unavailable), describes microbes degrading chlorinated ethenes and PCBs by replacing chlorine atoms with hydrogen. The Introduction also describes microbial metabolism as a means of pollutant detoxification. The claim extends this account to organic pollutants generally and to various catalytic mechanisms, neither of which these passages establish. (LLM, conf=0.84)

    Experimental — accuracy not yet measured
  • Engineered microbial communities could be used to clean up organic pollutants, and synthetic biology and genetic engineering can be used to improve the removal abilities of these strains.

    “The study shows that engineered microbial communities could be used to clean up organic pollutants.It shows how synthetic biology and genetic engineering can be used to improve the removal abilities of these strains [99].”

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Flagged first, then by citations

Research works printed but not linked: 169

  1. Rajajayavel, 2015, Enhanced reductive dechlorination of trichloroethylene by sulfidated nanoscale zerovalent iron, Water Res., 78, 144, 10.1016/j.watres.2015.04.009 · DOI
  2. Su, 2013, Removal of trichloroethylene by zerovalent iron/activated carbon derived from agricultural wastes, J. Environ. Manage., 129, 361, 10.1016/j.jenvman.2013.08.003 · DOI
  3. Dong, 2018, Factors influencing degradation of trichloroethylene by sulfide-modified nanoscale zero-valent iron in aqueous solution, Water Res., 135, 1, 10.1016/j.watres.2018.02.017 · DOI
  4. Huang, 2019, Persulfate activation by natural zeolite supported nanoscale zero-valent iron for trichloroethylene degradation in groundwater, Sci. Total Environ., 684, 351, 10.1016/j.scitotenv.2019.05.331 · DOI
  5. de Guzmán, 2018, Presence of organohalide-respiring bacteria in and around a permeable reactive barrier at a trichloroethylene-contaminated Superfund site, Environ. Pollut., 243, 766, 10.1016/j.envpol.2018.08.095 · DOI
  6. Shih, 2019, Characteristics of trichloroethene (TCE) dechlorination in seawater over a granulated zero-valent iron, Chemosphere, 216, 40, 10.1016/j.chemosphere.2018.10.059 · DOI
  7. Xie, 2017, The interactions between nanoscale zero-valent iron and microbes in the subsurface environment: a review, J. Hazard. Mater., 321, 390, 10.1016/j.jhazmat.2016.09.028 · DOI
  8. Usman, 2019, Characterization and utilization of aqueous products from hydrothermal conversion of biomass for bio-oil and hydro-char production: a review, Green Chem., 21, 1553, 10.1039/C8GC03957G · DOI · Paper page
  9. Usman, 2022, Current challenges of hydrothermal treated wastewater (HTWW) for environmental applications and their perspectives: a review, Environ. Res., 10.1016/j.envres.2022.113532 · DOI
  10. Li, 2019, Removal of hexavalent chromium from groundwater using sodium alginate dispersed nano zero-valent iron, J. Environ. Manage., 244, 33, 10.1016/j.jenvman.2019.04.130 · DOI
  11. Zhu, 2018, Green synthesis of nano zero-valent iron/Cu by green tea to remove hexavalent chromium from groundwater, J. Clean. Prod., 174, 184, 10.1016/j.jclepro.2017.10.302 · DOI
  12. Lien, 2016, Enhanced bioremediation of TCE-contaminated groundwater with coexistence of fuel oil: effectiveness and mechanism study, Chem. Eng. J., 289, 525, 10.1016/j.cej.2016.01.011 · DOI
  13. Dutta, 2022, An insight into valorization of lignocellulosic biomass by optimization with the combination of hydrothermal (HT) and biological techniques: a review, Sustain. Chem., 3, 35, 10.3390/suschem3010003 · DOI
  14. Majone, 2015, In situ groundwater and sediment bioremediation: barriers and perspectives at European contaminated sites, N. Biotechnol., 32, 133, 10.1016/j.nbt.2014.02.011 · DOI
  15. Mayer-Blackwell, 2017, Survival of vinyl chloride respiring Dehalococcoides mccartyi under long-term electron donor limitation, Environ. Sci. Technol., 51, 1635, 10.1021/acs.est.6b05050 · DOI
  16. Usman, 2014, Alkaline extraction of starch from broken rice of Pakistan, Int. J. Innov. Appl. Stud., 7, 146
  17. Zhang, 2016, An overview of remediation technologies for sites contaminated with volatile organic compounds, Geo-Chicago, 2016, 295
  18. Usman, 2014, Effects of Temperature, pH and Steeping Time on the Extraction of Starch from Pakistani Rice, Int. J. Scientific Engr. Res., 877
  19. Juwarkar, 2010, A comprehensive overview of elements in bioremediation, Rev. Environ. Sci. Biotechnol., 9, 215, 10.1007/s11157-010-9215-6 · DOI · Paper page
  20. Card, 2017, History of EPI Suite™ and future perspectives on chemical property estimation in US Toxic Substances Control Act new chemical risk assessments, Environ. Sci.: Process. Impacts, 19, 203
  21. Sung, 2006, Geobacter lovleyi sp. nov. strain SZ, a novel metal-reducing and tetrachloroethene-dechlorinating bacterium, Appl. Environ. Microbiol., 72, 2775, 10.1128/AEM.72.4.2775-2782.2006 · DOI
  22. Löffler, 2013, Int. J. Syst. Evol. Microbiol., 63, 625, 10.1099/ijs.0.034926-0 · DOI
  23. Amos, 2007, Experimental evaluation and mathematical modeling of microbially enhanced tetrachloroethene (PCE) dissolution, Environ. Sci. Technol., 41, 963, 10.1021/es061438n · DOI
  24. Ji, 2022, Effects of different feedstocks-based biochar on soil remediation: a review, Environ. Pollut., 294, 10.1016/j.envpol.2021.118655 · DOI
  25. Wang, 2016, Integration of organohalide-respiring bacteria and nanoscale zero-valent iron (Bio-nZVI-RD): a perfect marriage for the remediation of organohalide pollutants?, Biotechnol. Adv., 34, 1384, 10.1016/j.biotechadv.2016.10.004 · DOI
  26. Bennett, 2007, In situ reductive dechlorination of chlorinated ethenes in high nitrate groundwater, J. Hazard. Mater., 149, 568, 10.1016/j.jhazmat.2007.06.092 · DOI
  27. Löffler, 2006, Harnessing microbial activities for environmental cleanup, Curr. Opin. Biotechnol., 17, 274, 10.1016/j.copbio.2006.05.001 · DOI
  28. Kang, 2012, Biodegradation of trichloroethylene by an endophyte of hybrid poplar, Appl. Environ. Microbiol., 78, 3504, 10.1128/AEM.06852-11 · DOI
  29. Liang, 2018, Exposure to vinyl chloride and its influence on western diet-induced cardiac remodeling, Chem. Res. Toxicol., 31, 482, 10.1021/acs.chemrestox.8b00043 · DOI
  30. El-Shahawi, 2010, An overview on the accumulation, distribution, transformations, toxicity and analytical methods for the monitoring of persistent organic pollutants, Talanta, 80, 1587, 10.1016/j.talanta.2009.09.055 · DOI
  31. Breivik, 2007, Towards a global historical emission inventory for selected PCB congeners—A mass balance approach: 3. An update, Sci. Total Environ., 377, 296, 10.1016/j.scitotenv.2007.02.026 · DOI
  32. Kjellerup, 2008, Site-specific microbial communities in three PCB-impacted sediments are associated with different in situ dechlorinating activities, Environ. Microbiol., 10, 1296, 10.1111/j.1462-2920.2007.01543.x · DOI
  33. Perez-de-Mora, 2014, Bioremediation of chlorinated ethenes in fractured bedrock and associated changes in dechlorinating and nondechlorinating microbial populations, Environ. Sci. Technol., 48, 5770, 10.1021/es404122y · DOI
  34. Khan, 2022, A review of recent advancements in pretreatment techniques of lignocellulosic materials for biogas production: opportunities and Limitations, Chem. Eng. J. Adv., 10.1016/j.ceja.2022.100263 · DOI
  35. Liang, 2017, Temporal abundance and activity trends of vinyl chloride (VC)-degrading bacteria in a dilute VC plume at Naval Air Station Oceana, Environ. Sci. Pollut. Res., 24, 13760, 10.1007/s11356-017-8948-y · DOI
  36. DiStefano, 1999, The effect of tetrachloroethene on biological dechlorination of vinyl chloride: potential implication for natural bioattenuation, Water Res., 33, 1688, 10.1016/S0043-1354(98)00374-1 · DOI
  37. Xu, 2016, Microbial-catalyzed reductive dechlorination of polychlorinated biphenyls in Hudson and Grasse River sediment microcosms: determination of dechlorination preferences and identification of rare ortho removal pathways, Environ. Sci. Technol., 50, 12767, 10.1021/acs.est.6b03892 · DOI
  38. Dudková, 2012, Sediment-free anaerobic microbial enrichments with novel dechlorinating activity against highly chlorinated commercial PCBs, J. Chem. Technol. Biotechnol., 87, 1254, 10.1002/jctb.3807 · DOI
  39. Bedard, 2005, Characterization of the PCB substrate range of microbial dechlorination process LP, Environ. Sci. Technol., 39, 6831, 10.1021/es050255i · DOI
  40. Hughes, 2010, Identification of structural properties associated with polychlorinated biphenyl dechlorination processes, Environ. Sci. Technol., 44, 2842, 10.1021/es902109w · DOI
  41. Bedard, 2007, The Dehalococcoides population in sediment-free mixed cultures metabolically dechlorinates the commercial polychlorinated biphenyl mixture Aroclor 1260, Appl. Environ. Microbiol., 73, 2513, 10.1128/AEM.02909-06 · DOI
  42. Wiegel, 2000, Microbial reductive dehalogenation of polychlorinated biphenyls, FEMS Microbiol. Ecol., 32, 1, 10.1111/j.1574-6941.2000.tb00693.x · DOI
  43. Bedard, 1997, Enrichment of microorganisms that sequentially meta, para-dechlorin-ate the residue of aroclor 1260 in Housatonic River sediment, Environ. Sci. Technol., 31, 3308, 10.1021/es9703483 · DOI
  44. Abe, 2009, Evaluating the fate of chlorinated ethenes in streambed sediments by combining stable isotope, geochemical and microbial methods, J. Contam. Hydrol., 107, 10, 10.1016/j.jconhyd.2009.03.002 · DOI
  45. Futagami, 2009, Dehalogenation activities and distribution of reductive dehalogenase homologous genes in marine subsurface sediments, Appl. Environ. Microbiol., 75, 6905, 10.1128/AEM.01124-09 · DOI
  46. Yang, 2017, Grape pomace compost harbors organohalide-respiring Dehalogenimonas species with novel reductive dehalogenase genes, ISME J, 11, 2767, 10.1038/ismej.2017.127 · DOI
  47. Clark, 2018, Normalized quantitative PCR measurements as predictors for ethene formation at sites impacted with chlorinated ethenes, Environ. Sci. Technol., 52, 13410, 10.1021/acs.est.8b04373 · DOI
  48. Krzmarzick, 2012, Natural niche for organohalide-respiring Chloroflexi, Appl. Environ. Microbiol., 78, 393, 10.1128/AEM.06510-11 · DOI
  49. Ren, 2020, Hydrochar-facilitated anaerobic digestion: evidence for direct interspecies electron transfer mediated through surface oxygen-containing functional groups, Environ. Sci. Technol., 54, 5755, 10.1021/acs.est.0c00112 · DOI
  50. Usman, 2019, Molecular and microbial insights towards understanding the anaerobic digestion of the wastewater from hydrothermal liquefaction of sewage sludge facilitated by granular activated carbon (GAC), Environ. Int., 133, 10.1016/j.envint.2019.105257 · DOI
  51. Lee, 2012, Complete chloroform dechlorination by organochlorine respiration and fermentation, Environ. Microbiol., 14, 883, 10.1111/j.1462-2920.2011.02656.x · DOI
  52. Justicia-Leon, 2014, Bioaugmentation with distinct Dehalobacter strains achieves chloroform detoxification in microcosms, Environ. Sci. Technol., 48, 1851, 10.1021/es403582f · DOI
  53. Chang, 2011, Isolation and characterization of tetrachloroethylene-and cis-1, 2-dichloroethylene-dechlorinating propionibacteria, J. Ind. Microbiol. Biotechnol., 38, 1667, 10.1007/s10295-011-0956-1 · DOI
  54. Xu, 2012, Comprehensive assessment of bacterial communities and analysis of PCB congeners in PCB-contaminated sediment with depth, J. Environ. Eng., 138, 1167, 10.1061/(ASCE)EE.1943-7870.0000595 · DOI
  55. Watts, 2001, Comparative analysis of polychlorinated biphenyl-dechlorinating communities in enrichment cultures using three different molecular screening techniques, Environ. Microbiol., 3, 710, 10.1046/j.1462-2920.2001.00247.x · DOI
  56. Pulliam Holoman, 1998, Characterization of a defined 2, 3, 5, 6-tetrachlorobiphenyl-ortho-dechlorinating microbial community by comparative sequence analysis of genes coding for 16S rRNA, Appl. Environ. Microbiol., 64, 3359, 10.1128/AEM.64.9.3359-3367.1998 · DOI
  57. Fennell, 2004, Dehalococcoides ethenogenes strain 195 reductively dechlorinates diverse chlorinated aromatic pollutants, Environ. Sci. Technol., 38, 2075, 10.1021/es034989b · DOI
  58. Adrian, 2009, Dehalococcoides” sp. strain CBDB1 extensively dechlorinates the commercial polychlorinated biphenyl mixture Aroclor 1260, Appl. Environ. Microbiol., 75, 4516, 10.1128/AEM.00102-09 · DOI
  59. Cheng, 2009, Isolation and characterization of “Dehalococcoides” sp. strain MB, which dechlorinates tetrachloroethene to trans-1, 2-dichloroethene, Appl. Environ. Microbiol., 75, 5910, 10.1128/AEM.00767-09 · DOI
  60. Wang, 2019, Microbial synergistic interactions for reductive dechlorination of polychlorinated biphenyls, Sci. Total Environ., 666, 368, 10.1016/j.scitotenv.2019.02.283 · DOI
  61. Chow, 2010, Identification and transcriptional analysis of trans-DCE-producing reductive dehalogenases in Dehalococcoides species, ISME J, 4, 1020, 10.1038/ismej.2010.27 · DOI
  62. Wang, 2014, Genomic characterization of three unique Dehalococcoides that respire on persistent polychlorinated biphenyls, Proc. Natl. Acad. Sci., 111, 12103, 10.1073/pnas.1404845111 · DOI
  63. He, 2007, Influence of vitamin B12 and cocultures on the growth of Dehalococcoides isolates in defined medium, Appl. Environ. Microbiol., 73, 2847, 10.1128/AEM.02574-06 · DOI
  64. Men, 2012, Sustainable syntrophic growth of Dehalococcoides ethenogenes strain 195 with Desulfovibrio vulgaris Hildenborough and Methanobacterium congolense: global transcriptomic and proteomic analyses, ISME J, 6, 410, 10.1038/ismej.2011.111 · DOI
  65. Ding, 2018, Growth of Dehalococcoides mccartyi species in an autotrophic consortium producing limited acetate, Biodegradation, 29, 487, 10.1007/s10532-018-9846-9 · DOI
  66. Ismaeil, 2018, Bacteroides sedimenti sp. nov., isolated from a chloroethenes-dechlorinating consortium enriched from river sediment, J. Microbiol., 56, 619, 10.1007/s12275-018-8187-z · DOI
  67. Zhuang, 2011, Dehalogenation of polybrominated diphenyl ethers and polychlorinated biphenyl by bimetallic, impregnated, and nanoscale zerovalent iron, Environ. Sci. Technol., 45, 4896, 10.1021/es104312h · DOI
  68. Ishag, 2016, Biodegradation of chlorpyrifos, malathion, and dimethoate by three strains of bacteria isolated from pesticide-polluted soils in Sudan, J. Agric. Food Chem., 64, 8491, 10.1021/acs.jafc.6b03334 · DOI
  69. Viesser, 2020, Petroleum-tolerant rhizospheric bacteria: isolation, characterization and bioremediation potential, Sci. Rep., 10, 1, 10.1038/s41598-020-59029-9 · DOI
  70. Zhang, 2021, Genetically engineered thermotolerant facultative anaerobes for high-efficient degradation of multiple hazardous nitroalkanes, J. Hazard. Mater., 405, 10.1016/j.jhazmat.2020.124253 · DOI
  71. Dvořák, 2017, Bioremediation 3.0: engineering pollutant-removing bacteria in the times of systemic biology, Biotechnol. Adv., 35, 845, 10.1016/j.biotechadv.2017.08.001 · DOI
  72. Joutey, 2013, Biodegradation: involved microorganisms and genetically engineered microorganisms, 1, 289
  73. DeLorenzo, 2019, Construction of genetic logic gates based on the T7 RNA polymerase expression system in Rhodococcus opacus PD630, ACS Synth. Biol., 8, 1921, 10.1021/acssynbio.9b00213 · DOI
  74. Ofaim, 2020, Genome-scale reconstruction of Paenarthrobacter aurescens TC1 metabolic model towards the study of atrazine bioremediation, Sci. Rep., 10, 1, 10.1038/s41598-020-69509-7 · DOI
  75. Young, 2021, Combinatorial metabolic pathway assembly approaches and toolkits for modular assembly, Metab. Eng., 63, 81, 10.1016/j.ymben.2020.12.001 · DOI
  76. Đurđić, 2020, Saturation mutagenesis to improve the degradation of azo dyes by versatile peroxidase and application in form of VP-coated yeast cell walls, Enzyme Microb. Technol., 136
  77. Nikel, 2013, Engineering an anaerobic metabolic regime in Pseudomonas putida KT2440 for the anoxic biodegradation of 1, 3-dichloroprop-1-ene, Metab. Eng., 15, 98, 10.1016/j.ymben.2012.09.006 · DOI
  78. Lu, 2021, Waste activated sludge stimulates in situ microbial reductive dehalogenation of organohalide-contaminated soil, J. Hazard. Mater., 411, 10.1016/j.jhazmat.2021.125189 · DOI
  79. Usman, 2021, Microbial insights towards understanding the role of hydrochar in alleviating ammonia inhibition during anaerobic digestion, Chem. Eng. J., 419, 10.1016/j.cej.2021.129541 · DOI
  80. Shi, 2021, Combined microbial transcript and metabolic analysis reveals the different roles of hydrochar and biochar in promoting anaerobic digestion of waste activated sludge, Water Res., 205, 10.1016/j.watres.2021.117679 · DOI
  81. Ji, 2020, Molecular and microbial insights towards understanding the effects of hydrochar on methane emission from paddy soil, Sci. Total Environ., 714, 10.1016/j.scitotenv.2020.136769 · DOI
  82. Shi, 2021, Genome-centric metatranscriptomics analysis reveals the role of hydrochar in anaerobic digestion of waste activated sludge, Environ. Sci. Technol., 55, 8351, 10.1021/acs.est.1c01995 · DOI
  83. Albers, 2015, Degradation of trace concentrations of the persistent groundwater pollutant 2, 6-dichlorobenzamide (BAM) in bioaugmented rapid sand filters, Water Res., 83, 61, 10.1016/j.watres.2015.06.023 · DOI
  84. Usman, 2020, Hydrochar promoted anaerobic digestion of hydrothermal liquefaction wastewater: focusing on the organic degradation and microbial community, Chem. Eng. J., 399, 10.1016/j.cej.2020.125766 · DOI
  85. Baric, 2012, Coupling of polyhydroxybutyrate (PHB) and zero valent iron (ZVI) for enhanced treatment of chlorinated ethanes in permeable reactive barriers (PRBs), Chem. Eng. J., 195, 22, 10.1016/j.cej.2012.04.026 · DOI
  86. Usman, 2020, Characterization and biogas production potentials of aqueous phase produced from hydrothermal carbonization of biomass–Major components and their binary mixtures, Chem. Eng. J., 388, 10.1016/j.cej.2020.124201 · DOI
  87. Hao, 2020, Molecular composition of hydrothermal liquefaction wastewater from sewage sludge and its transformation during anaerobic digestion, J. Hazard. Mater., 383, 10.1016/j.jhazmat.2019.121163 · DOI
  88. McGuire, 2004, Historical analysis of monitored natural attenuation: a survey of 191 chlorinated solvent sites and 45 solvent plumes, Remediation Journal: The Journal of Environmental Cleanup Costs, Technologies & Techniques, 15, 99, 10.1002/rem.20036 · DOI
  89. Pakdeesusuk, 2005, Assessment of natural attenuation via in situ reductive dechlorination of polychlorinated biphenyls in sediments of the Twelve Mile Creek arm of Lake Hartwell, SC, Environ. Sci. Technol., 39, 945, 10.1021/es0491228 · DOI
  90. Hashmi, 2016, PCBs attenuation and abundance of Dehalococcoides spp., bphC, CheA, and flic genes in typical polychlorinated biphenyl-polluted soil under floody and dry soil conditions, Environ. Sci. Pollut. Res., 23, 3907, 10.1007/s11356-015-5577-1 · DOI
  91. Scheutz, 2008, Concurrent ethene generation and growth of Dehalococcoides containing vinyl chloride reductive dehalogenase genes during an enhanced reductive dechlorination field demonstration, Environ. Sci. Technol., 42, 9302, 10.1021/es800764t · DOI
  92. He, 2003, Detoxification of vinyl chloride to ethene coupled to growth of an anaerobic bacterium, Nature, 424, 62, 10.1038/nature01717 · DOI
  93. Aulenta, 2007, Field study of in situ anaerobic bioremediation of a chlorinated solvent source zone, Ind. Eng. Chem. Res., 46, 6812, 10.1021/ie070048m · DOI
  94. Hood, 2008, Demonstration of enhanced bioremediation in a TCE source area at Launch Complex 34, Cape Canaveral Air Force Station, Ground Water Monit. Remediat., 28, 98, 10.1111/j.1745-6592.2008.00197.x · DOI
  95. Matturro, 2018, Microbial community changes in a chlorinated solvents polluted aquifer over the field scale treatment with poly-3-hydroxybutyrate as amendment, Front. Microbiol., 9, 1664, 10.3389/fmicb.2018.01664 · DOI
  96. Borden, 2007, Enhanced anaerobic bioremediation of a TCE source at the Tarheel Army Missile Plant using EOS, Remediation Journal: The Journal of Environmental Cleanup Costs, Technologies & Techniques, 17, 5, 10.1002/rem.20130 · DOI
  97. Kocur, 2016, Long-term field study of microbial community and dechlorinating activity following carboxymethyl cellulose-stabilized nanoscale zero-valent iron injection, Environ. Sci. Technol., 50, 7658, 10.1021/acs.est.6b01745 · DOI
  98. Hanada, 1998, Phylogenetic analysis of trichloroethylene-degrading bacteria newly isolated from soil polluted with this contaminant, J. Ferment. Bioeng., 86, 539, 10.1016/S0922-338X(99)80003-8 · DOI
  99. Eguchi, 2001, A field evaluation of in situ biodegradation of trichloroethylene through methane injection, Water Res., 35, 2145, 10.1016/S0043-1354(00)00494-2 · DOI
  100. Maymo-Gatell, 1997, Isolation of a bacterium that reductively dechlorinates tetrachloroethene to ethene, Science, 276, 1568, 10.1126/science.276.5318.1568 · DOI
  101. Yang, 2018, In situ remediation of chlorinated solvent-contaminated groundwater using ZVI/organic carbon amendment in China: field pilot test and full-scale application, Environ. Sci. Pollut. Res., 25, 5051, 10.1007/s11356-017-9903-7 · DOI
  102. Atashgahi, 2017, Geochemical and microbial community determinants of reductive dechlorination at a site biostimulated with glycerol, Environ. Microbiol., 19, 968, 10.1111/1462-2920.13531 · DOI
  103. Sheu, 2016, Application of NZVI-contained emulsified substrate to bioremediate PCE-contaminated groundwater–A pilot-scale study, Chem. Eng. J., 304, 714, 10.1016/j.cej.2016.06.126 · DOI
  104. Adetutu, 2015, Exploiting the intrinsic microbial degradative potential for field-based in situ dechlorination of trichloroethene contaminated groundwater, J. Hazard. Mater., 300, 48, 10.1016/j.jhazmat.2015.06.055 · DOI
  105. Strycharz, 2008, Graphite electrode as a sole electron donor for reductive dechlorination of tetrachlorethene by Geobacter lovleyi, Appl. Environ. Microbiol., 74, 5943, 10.1128/AEM.00961-08 · DOI
  106. Lohner, 2011, Sequential reductive and oxidative biodegradation of chloroethenes stimulated in a coupled bioelectro-process, Environ. Sci. Technol., 45, 6491, 10.1021/es200801r · DOI
  107. Sowers, 2013, In situ treatment of PCBs by anaerobic microbial dechlorination in aquatic sediment: are we there yet?, Curr. Opin. Biotechnol., 24, 482, 10.1016/j.copbio.2012.10.004 · DOI
  108. Sharma, 2018, Advances and perspective in bioremediation of polychlorinated biphenyl-contaminated soils, Environ. Sci. Pollut. Res., 25, 16355, 10.1007/s11356-017-8995-4 · DOI
  109. Wu, 2000, Establishment of a polychlorinated biphenyl-dechlorinating microbial consortium, specific for doubly flanked chlorines, in a defined, sediment-free medium, Appl. Environ. Microbiol., 66, 49, 10.1128/AEM.66.1.49-53.2000 · DOI
  110. Chang, 2001, Microbial dechlorination of three PCB congeners in river sediment, Chemosphere, 45, 849, 10.1016/S0045-6535(01)00106-0 · DOI
  111. Yan, 2006, The effect of varying levels of sodium bicarbonate on polychlorinated biphenyl dechlorination in Hudson River sediment cultures, Environ. Microbiol., 8, 1288, 10.1111/j.1462-2920.2006.01037.x · DOI
  112. Bedard, 1995, Characterization of the polychlorinated biphenyls in the sediments of Woods Pond: evidence for microbial dechlorination of Aroclor 1260 in situ, Environ. Sci. Technol., 30, 237, 10.1021/es950262e · DOI
  113. Bedard, 1998, Brominated biphenyls prime extensive microbial reductive dehalogenation of Aroclor 1260 in Housatonic River sediment, Appl. Environ. Microbiol., 64, 1786, 10.1128/AEM.64.5.1786-1795.1998 · DOI
  114. Cai, 2018, A novel Aroclor 1242-degrading culturable endophytic bacterium isolated from tissue culture seedlings of Salix matsudana f. pendula Schneid, Phytochem. Lett., 23, 66, 10.1016/j.phytol.2017.11.012 · DOI
  115. Srinivasa Varadhan, 2011, Effect of biostimulation on the microbial community in PCB-contaminated sediments through periodic amendment of sediment with iron, J. Ind. Microbiol. Biotechnol., 38, 1691, 10.1007/s10295-011-0959-y · DOI
  116. Liu, 2017, Addition of iron oxides in sediments enhances 2, 3, 4, 5-tetrachlorobiphenyl (PCB 61) dechlorination by low-voltage electric fields, RSC Adv., 7, 26019, 10.1039/C7RA02849K · DOI
  117. Chun, 2013, Electrical stimulation of microbial PCB degradation in sediment, Water Res., 47, 141, 10.1016/j.watres.2012.09.038 · DOI
  118. Wan, 2018, Time-dependent bacterial community and electrochemical characterizations of cathodic biofilms in the surfactant-amended sediment-based bioelectrochemical reactor with enhanced 2, 3, 4, 5-tetrachlorobiphenyl dechlorination, Environ. Pollut., 236, 343, 10.1016/j.envpol.2018.01.048 · DOI
  119. Mao, 2012, Electrokinetic-enhanced bioaugmentation for remediation of chlorinated solvents contaminated clay, J. Hazard. Mater., 213, 311, 10.1016/j.jhazmat.2012.02.001 · DOI
  120. Dolinová, 2017, Microbial degradation of chloroethenes: a review, Environ. Sci. Pollut. Res., 24, 13262, 10.1007/s11356-017-8867-y · DOI
  121. Major, 2002, Field demonstration of successful bioaugmentation to achieve dechlorination of tetrachloroethene to ethene, Environ. Sci. Technol., 36, 5106, 10.1021/es0255711 · DOI
  122. Chiu, 2013, Evaluation of enhanced reductive dechlorination of trichloroethylene using gene analysis: pilot-scale study, J. Environ. Eng., 139, 428, 10.1061/(ASCE)EE.1943-7870.0000654 · DOI
  123. Xu, 2019, Reduction in sulfate inhibition of microbial dechlorination of polychlorinated biphenyls in Hudson and Grasse River sediments through fatty acid supplementation, Chemosphere, 233, 81, 10.1016/j.chemosphere.2019.05.211 · DOI
  124. Fagervold, 2011, Effects of bioaugmentation on indigenous PCB dechlorinating activity in sediment microcosms, Water Res., 45, 3899, 10.1016/j.watres.2011.04.048 · DOI
  125. Cho, 2003, Reductive dechlorination of polychlorinated biphenyls: threshold concentration and dechlorination kinetics of individual congeners in Aroclor 1248, Environ. Sci. Technol., 37, 5651, 10.1021/es034600k · DOI
  126. Payne, 2013, Remediation of polychlorinated biphenyl impacted sediment by concurrent bioaugmentation with anaerobic halorespiring and aerobic degrading bacteria, Environ. Sci. Technol., 47, 3807, 10.1021/es304372t · DOI
  127. Payne, 2017, Mesocosm studies on the efficacy of bioamended activated carbon for treating PCB-impacted sediment, Environ. Sci. Technol., 51, 10691, 10.1021/acs.est.7b01935 · DOI
  128. Payne, 2019, A pilot-scale field study: in situ treatment of PCB-impacted sediments with bioamended activated carbon, Environ. Sci. Technol., 53, 2626, 10.1021/acs.est.8b05019 · DOI
  129. Passatore, 2014, Phytoremediation and bioremediation of polychlorinated biphenyls (PCBs): state of knowledge and research perspectives, J. Hazard. Mater., 278, 189, 10.1016/j.jhazmat.2014.05.051 · DOI
  130. Xiu, 2010, Effect of bare and coated nanoscale zerovalent iron on tceA and vcrA gene expression in Dehalococcoides spp, Environ. Sci. Technol., 44, 7647, 10.1021/es101786y · DOI
  131. Steliga, 2020, Assessment of biodegradation efficiency of polychlorinated biphenyls (PCBs) and petroleum hydrocarbons (TPH) in soil using three individual bacterial strains and their mixed culture, Molecules, 25, 709, 10.3390/molecules25030709 · DOI
  132. Horváthová, 2018, Bioremediation of PCB-contaminated shallow river sediments: the efficacy of biodegradation using individual bacterial strains and their consortia, Chemosphere, 193, 270, 10.1016/j.chemosphere.2017.11.012 · DOI
  133. Xing, 2020, Degradation mechanism of 4-chlorobiphenyl by consortium of Pseudomonas sp. strain CB-3 and Comamonas sp. strain CD-2, Curr. Microbiol., 77, 15, 10.1007/s00284-019-01791-9 · DOI
  134. Mikesková, 2012, Interspecific interactions in mixed microbial cultures in a biodegradation perspective, Appl. Microbiol. Biotechnol., 95, 861, 10.1007/s00253-012-4234-6 · DOI
  135. Su, 2015, Culture-dependent and culture-independent characterization of potentially functional biphenyl-degrading bacterial community in response to extracellular organic matter from M icrococcus luteus, Microb. Biotechnol., 8, 569, 10.1111/1751-7915.12266 · DOI
  136. Hayat, 2019, Organic and chemical amendments positively modulate the bacterial proliferation for effective rhizoremediation of PCBs-contaminated soil, Ecol. Eng., 138, 412, 10.1016/j.ecoleng.2019.07.038 · DOI
  137. Teng, 2016, Isolation of the PCB-degrading bacteria Mesorhizobium sp. ZY1 and its combined remediation with Astragalus sinicus L. for contaminated soil, Int. J. Phytoremediation, 18, 141, 10.1080/15226514.2015.1073667 · DOI
  138. Liang, 2014, Enhanced polychlorinated biphenyl removal in a switchgrass rhizosphere by bioaugmentation with Burkholderia xenovorans LB400, Ecol. Eng., 71, 215, 10.1016/j.ecoleng.2014.07.046 · DOI
  139. Salimizadeh, 2018, Coupling of bioaugmentation and phytoremediation to improve PCBs removal from a transformer oil-contaminated soil, Int. J. Phytoremediation, 20, 658, 10.1080/15226514.2017.1393388 · DOI
  140. Jing, 2018, Remediation of polychlorinated biphenyls (PCBs) in contaminated soils and sediment: state of knowledge and perspectives, Front. Environ. Sci., 6, 79, 10.3389/fenvs.2018.00079 · DOI
  141. Khreis, 2017, Exposure to traffic-related air pollution and risk of development of childhood asthma: a systematic review and meta-analysis, Environ. Int., 100, 1, 10.1016/j.envint.2016.11.012 · DOI
  142. Liu, 2018, Climatic role of terrestrial ecosystem under elevated CO 2: a bottom-up greenhouse gases budget, Ecol. Lett., 21, 1108, 10.1111/ele.13078 · DOI
  143. Huang, 2019, Current status of agricultural soil pollution by heavy metals in China: a meta-analysis, Sci. Total Environ., 651, 3034, 10.1016/j.scitotenv.2018.10.185 · DOI
  144. Yuan, 2021, Potential role of methanogens in microbial reductive dechlorination of organic chlorinated pollutants in Situ, Environ. Sci. Technol., 55, 5917, 10.1021/acs.est.0c08631 · DOI
  145. May, 2008, Dehalorespiration with polychlorinated biphenyls by an anaerobic ultramicrobacterium, Appl. Environ. Microbiol., 74, 2089, 10.1128/AEM.01450-07 · DOI
  146. LaRoe, 2014, Dehalococcoides mccartyi strain JNA in pure culture extensively dechlorinates Aroclor 1260 according to polychlorinated biphenyl (PCB) dechlorination process N, Environ. Sci. Technol., 48, 9187, 10.1021/es500872t · DOI
  147. Cutter, 2001, Identification of a microorganism that links its growth to the reductive dechlorination of 2, 3, 5, 6-chlorobiphenyl, Environ. Microbiol., 3, 699, 10.1046/j.1462-2920.2001.00246.x · DOI
  148. Bunge, 2003, Reductive dehalogenation of chlorinated dioxins by an anaerobic bacterium, Nature, 421, 357, 10.1038/nature01237 · DOI
  149. Lin, 2016, Bioremediation of OCDF-contaminated soils by novel bacterial strain, Appl. Ecol. Env. Res, 15, 713, 10.15666/aeer/1503_713723 · DOI
  150. Bunge, 2008, Enrichment of a dioxin-dehalogenating Dehalococcoides species in two-liquid phase cultures, Environ. Microbiol., 10, 2670, 10.1111/j.1462-2920.2008.01688.x · DOI
  151. Pöritz, 2015, Dehalococcoides mccartyi strain DCMB5 respires a broad spectrum of chlorinated aromatic compounds, Appl. Environ. Microbiol., 81, 587, 10.1128/AEM.02597-14 · DOI
  152. Ballerstedt, 2004, Properties of a trichlorodibenzo-p-dioxin-dechlorinating mixed culture with a Dehalococcoides as putative dechlorinating species, FEMS Microbiol. Ecol., 47, 223, 10.1016/S0168-6496(03)00282-4 · DOI
  153. Pathiraja, 2019, Solubilization and degradation of polychlorinated biphenyls (PCBs) by naturally occurring facultative anaerobic bacteria, Sci. Total Environ., 651, 2197, 10.1016/j.scitotenv.2018.10.127 · DOI
  154. Murínová, 2014, Degradation of polychlorinated biphenyls (PCBs) by four bacterial isolates obtained from the PCB-contaminated soil and PCB-contaminated sediment, Int. Biodeterior. Biodegradation, 91, 52, 10.1016/j.ibiod.2014.03.011 · DOI
  155. Qiu, 2016, Isolation and characterization of a cold-resistant PCB209-degrading bacterial strain from river sediment and its application in bioremediation of contaminated soil, J. Environ. Sci. Health, Part A, 51, 204, 10.1080/10934529.2015.1094324 · DOI
  156. Shuai, 2016, Regional analysis of potential polychlorinated biphenyl degrading bacterial strains from China, Brazilian J. Microbiol., 47, 536, 10.1016/j.bjm.2014.12.001 · DOI
  157. Nam, 2014, Biodegradation of biphenyl and 2-chlorobiphenyl by a Pseudomonas sp. KM-04 isolated from PCBs-contaminated coal mine soil, Bull. Environ. Contam. Toxicol., 93, 89, 10.1007/s00128-014-1286-6 · DOI
  158. Voronina, 2019, Diversity of the bphA1 genes in a microbial community from anthropogenically contaminated soil and isolation of new Pseudomonads degrading biphenyl/chlorinated biphenyls, Microbiology, 88, 433, 10.1134/S0026261719030172 · DOI
  159. Wang, 2018, Biodegradation and chemotaxis of polychlorinated biphenyls, biphenyls, and their metabolites by Rhodococcus spp, Biodegradation, 29, 1, 10.1007/s10532-017-9809-6 · DOI
  160. Sandhu, 2020, Evaluation of biphenyl-and polychlorinated-biphenyl (PCB) degrading Rhodococcus sp. MAPN-1 on growth of Morus alba by pot study, Int. J. Phytoremediation, 22, 1487, 10.1080/15226514.2020.1784088 · DOI
  161. Garrido-Sanz, 2020, Analysis of the biodegradative and adaptive potential of the novel polychlorinated biphenyl degrader Rhodococcus sp. WAY2 revealed by its complete genome sequence, Microb. Genom., 6
  162. Hu, 2015, Sphingobium fuliginis HC3: a novel and robust isolated biphenyl-and polychlorinated biphenyls-degrading bacterium without dead-end intermediates accumulation, PLoS ONE, 10, 10.1371/journal.pone.0122740 · DOI
  163. Mizukami-Murata, 2016, Detoxification of hydroxylated polychlorobiphenyls by Sphingomonas sp. strain N-9 isolated from forest soil, Chemosphere, 165, 173, 10.1016/j.chemosphere.2016.08.127 · DOI
  164. Ellis, 2000, Bioaugmentation for accelerated in situ anaerobic bioremediation, Environ. Sci. Technol., 34, 2254, 10.1021/es990638e · DOI
  165. Lee, 2008, Quantifying genes and transcripts to assess the in situ physiology of “Dehalococcoides” spp. in a trichloroethene-contaminated groundwater site, Appl. Environ. Microbiol., 74, 2728, 10.1128/AEM.02199-07 · DOI
  166. Schaefer, 2010, Field-scale evaluation of bioaugmentation dosage for treating chlorinated ethenes, Ground Water Monit. Remediat., 30, 113, 10.1111/j.1745-6592.2010.01297.x · DOI
  167. Verce, 2015, A long-term field study of in situ bioremediation in a fractured conglomerate trichloroethene source zone, Bioremediat. J., 19, 18, 10.1080/10889868.2014.978836 · DOI
  168. Schaefer, 2017, Bioaugmentation in a well-characterized fractured rock DNAPL source area, Ground Water Monit. Remediat., 37, 35, 10.1111/gwmr.12208 · DOI
  169. Damgaard, 2013, Performance of full-scale enhanced reductive dechlorination in clay till, Ground Water Monit. Remediat., 33, 48, 10.1111/j.1745-6592.2012.01405.x · DOI

Cited by

Sorted by citations

Metadata

Authors
Dutta, N., Usman, M., Ashraf, M. A., Luo, G., & Zhang, S.
Affiliations
  • Washington State University Tri-Cities (US)
  • Chinese Academy of Sciences (CN)
  • Fudan University (CN)
Corresponding author
  • Usman, Muhammad
  • Zhang, Shicheng
Venue
Chemical Engineering Journal Advances
Publisher
Elsevier BV
Published
2022-11
Volume
12
Pages
100359
ISSN
2666-8211 (ISSN-L)
OpenAlex
W4284970457
Cited by
58
References
1
Citations by year
2026: 10 · 2025: 17 · 2024: 17 · 2023: 8 · 2022: 6
FWCI
2.82
Type
journal article
Language
en
Open access
Locations
  • Chemical Engineering Journal Advances (publishedVersion, cc-by)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • China Scholarship Council (201,708,310,124)
  • National Natural Science Foundation of China (31,970,117)
  • Science and Technology Commission of Shanghai Municipality (19DZ1204704)
Topics
  • Physical Sciences › Environmental Science › Pollution › Microbial bioremediation and biosurfactants
  • Physical Sciences › Environmental Science › Environmental Engineering › Environmental remediation with nanomaterials
  • Physical Sciences › Environmental Science › Environmental Engineering › Microbial Fuel Cells and Bioremediation
Keywords
chloroethenes, polychlorinated biphenyls, in situ bioremediation, biostimulation, bioaugmentation, anaerobic bacteria, electron competition, groundwater contamination, soil contamination, methanogenic bacteria, iron-reducing bacteria, sulfate-reducing bacteria

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review