4.4 Article

High expression of ring-hydroxylating dioxygenase genes ensure efficient degradation of p-toluate, phthalate, and terephthalate by Comamonas testosteroni strain 3a2

Journal

ARCHIVES OF MICROBIOLOGY
Volume 203, Issue 7, Pages 4101-4112

Publisher

SPRINGER
DOI: 10.1007/s00203-021-02395-3

Keywords

Ring hydroxylating dioxygenases; Para-toluic acid; Toluate 1; 2-dioxygenase; Terephthalate 1; 2 dioxygenase; Phthalate 4; 5 dioxygenase; Biodegradation

Categories

Funding

  1. Ege University, Scientific Research Projects Fund [BAP FKB-2019-20395]
  2. inistry of Development Ege University Application and Research Center for Testing and Analysis (EGE-MATAL) [2010K120810]
  3. TUBTAK [112D044-TUBTAK]

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In this study, the ability of Comamonas testosteroni strain 3a2 to effectively degrade para-toluic acid was investigated. The strain was able to degrade up to 1000 mg/L of para-toluic acid within 14 hours, with the highest degradation yield observed in the presence of yeast extract as a nitrogen source. Additionally, genes for various dioxygenases were detected in the genomic DNA of 3a2, indicating their role in the degradation process.
Para-toluic acid, a major pollutant in industrial wastewater, is hazardous to human health. It has been demonstrated that Gram-negative bacteria are among the most effective degraders of para-toluic acid. In this study, the ability of Comamonas testosteroni strain 3a2, isolated from a petrochemical industry wastewater, to degrade para-toluic acid was investigated. The effect of different carbon (glucose and ethylene glycol) and nitrogen sources (urea, yeast extract, peptone, NaNO3, NH4NO3) on the biodegradation of para-toluic acid by the isolate 3a2 was evaluated. Furthermore, ring hydroxylating dioxygenase genes were amplified by PCR and their expression was evaluated during the biodegradation of para-toluic acid. The results indicated that strain 3a2 was able to degrade up to 1000 mg/L of para-toluic acid after 14 h. The highest degradation yield was recorded in the presence of yeast extract as nitrogen source. However, the formation of terephthalic acid and phthalic acid was noted during para-toluic acid degradation by the isolate 3a2. Toluate 1,2-dioxygenase, terephthalate 1,2 dioxygenase, and phthalate 4,5 dioxygenase genes were detected in the genomic DNA of 3a2. The induction of ring hydroxylating dioxygenase genes was proportional to the concentration of each hydrocarbon. This study showed that the isolate 3a2 can produce terephthalate and phthalate during the para-toluic acid biodegradation, which were also degraded after 24 h.

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