4.7 Article

Novel Mechanism and Kinetics of Tetramethrin Degradation Using an Indigenous Gordonia cholesterolivorans A16

期刊

出版社

MDPI
DOI: 10.3390/ijms22179242

关键词

tetramethrin; Gordonia cholesterolivorans; bioaugmentation; metabolites; metabolic pathways

资金

  1. Key Realm R&D Program of Guangdong Province, China [2018B020206001, 2020B0202090001]
  2. China Postdoctoral Science Foundation [2020M672655]
  3. Natural Science Foundation of Guangdong Province, China [2021A1515010889]
  4. National College Students' Innovation and Entrepreneurship Training Program, China [202110564068]
  5. Guangdong Special Branch Plan for Young Talent with Scientific and Technological Innovation, China [2017TQ04N026]

向作者/读者索取更多资源

The bacterial strain A16, identified as Gordonia cholesterolivorans, exhibited superior tetramethrin degradation activity. It efficiently degraded tetramethrin under various conditions and significantly accelerated the degradation of tetramethrin in contaminated soils, showing great potential for bioremediation.
Tetramethrin is a pyrethroid insecticide that is commonly used worldwide. The toxicity of this insecticide into the living system is an important concern. In this study, a novel tetramethrin-degrading bacterial strain named A16 was isolated from the activated sludge and identified as Gordonia cholesterolivorans. Strain A16 exhibited superior tetramethrin degradation activity, and utilized tetramethrin as the sole carbon source for growth in a mineral salt medium (MSM). High-performance liquid chromatography (HPLC) analysis revealed that the A16 strain was able to completely degrade 25 mg center dot L-1 of tetramethrin after 9 days of incubation. Strain A16 effectively degraded tetramethrin at temperature 20-40 degrees C, pH 5-9, and initial tetramethrin 25-800 mg center dot L-1. The maximum specific degradation rate (q(max)), half-saturation constant (K-s), and inhibition constant (K-i) were determined to be 0.4561 day(-1), 7.3 mg center dot L-1, and 75.2 mg center dot L-1, respectively. The Box-Behnken design was used to optimize degradation conditions, and maximum degradation was observed at pH 8.5 and a temperature of 38 degrees C. Five intermediate metabolites were identified after analyzing the degradation products through gas chromatography-mass spectrometry (GC-MS), which suggested that tetramethrin could be degraded first by cleavage of its carboxylester bond, followed by degradation of the five-carbon ring and its subsequent metabolism. This is the first report of a metabolic pathway of tetramethrin in a microorganism. Furthermore, bioaugmentation of tetramethrin-contaminated soils (50 mg center dot kg(-1)) with strain A16 (1.0 x 10(7) cells g(-1) of soil) significantly accelerated the degradation rate of tetramethrin, and 74.1% and 82.9% of tetramethrin was removed from sterile and non-sterile soils within 11 days, respectively. The strain A16 was also capable of efficiently degrading a broad spectrum of synthetic pyrethroids including D-cyphenothrin, chlorempenthrin, prallethrin, and allethrin, with a degradation efficiency of 68.3%, 60.7%, 91.6%, and 94.7%, respectively, after being cultured under the same conditions for 11 days. The results of the present study confirmed the bioremediation potential of strain A16 from a contaminated environment.

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