4.7 Article

Zn2+-dependent enhancement of Atrazine biodegradation by Klebsiella variicola FH-1

Journal

JOURNAL OF HAZARDOUS MATERIALS
Volume 411, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jhazmat.2021.125112

Keywords

Hydrolase; Flow cytometry; Gene knockout; Red homologous recombination; Bioactivity; Cell membrane permeability

Funding

  1. National Key Research and Development Program of China [2016YFD0200203]
  2. Project of Science and Technology Development of the Natural Science Foundation of Jilin Province, China [20200201215JC]
  3. Science and Technology Research Projects of Jilin Province, China [20190301063NY]

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The addition of Zn2+ improves the degradation efficiency of Atrazine by Klebsiella variicola FH-1. Knockout of ORFs encoding Zn2+-dependent hydrolases affects the degradation efficiency of Atrazine. The enzymatic activities of pydC encoded by ORF 3597 play a significant role in the degradation of Atrazine in the presence of Zn2+.
Degradation efficiency of Atrazine by Klebsiella variicola FH-1 is improved by the addition of Zn2+. Both the chromosome and plasmid genomes of strain FH-1 were sequenced and annotated to identify genes involved in the degradation of Atrazine. Four open reading frames (ORFs) 1040, 2582, 3597, and 4043 encoding Zn2+dependent hydrolases were knocked out to verify their predicted functions in the degradation of Atrazine. In the presence of Zn2+, the biodegradation efficiency of Atrazine by knockout mutant ?ORF 3597 was 13.7% lower than that of wild type (WT) of strain FH-1 but still 9.4% higher than that of WT without Zn2+. These results indicated that ORF 3597 played a synergistic role but may not be the sole factor involved in the degradation of Atrazine. The enzymatic activities of pydC encoded by ORF 3597 were further characterized in the degradation of Atrazine. Results of fluorescence staining and flow cytometry analyses showed that the survival of bacterial cells and cell membrane permeability were increased in the presence of Zn2+ at different concentrations. Our study provided a scientific foundation for further investigation of the biological mechanisms of improving the degradation of Atrazine by strain FH-1 with the presence of Zn2+.

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