Strategies and mechanisms for improving groundwater remediation efficiency of chlorinated ethenes by controlling the particle size of polyhydroxyalkanoate

Abstract

The efficacy of in-situ bioremediation of chlorinated ethenes (CEs)-contaminated groundwater is heavily contingent upon the provision of exogenous electron donors to facilitate reductive dechlorination by dechlorinating bacteria. Nonetheless, methanogenic archaea have been reported to engender competition for the limited electron donor supply, thereby diminishing dechlorination efficiency. This study proposes a novel strategy to enhance reductive dechlorination by reducing the particle size of polyhydroxyalkanoate (PHA) to the micrometer scale, thereby inhibiting methanogenic competition for electron donors. The results demonstrate that trichloroethylene (TCE) biodegradation efficiency peaked at a PHA particle size of 500 μm, significantly surpassing the efficiency observed in groups with particle sizes of 50 and 2000 μm. Furthermore, the electron utilization efficiency of dechlorinating bacteria (represented by Geobacter, Dehalobacter, Anaerolinea, etc in this study) was as high as 94.82 % over methanogenic archaea (represented by Methanobacterium) in the 500 μm group. Mechanistic analyses revealed that the 500 μm PHA particles activated dark oxygen, leading to the generation of reactive oxygen species that decreased the abundance of the methanogenic functional gene McrA and increased the abundance of dechlorinating functional gene TceA relative to the total microbial genome gene (in terms of 16S rRNA). In contrast, PHA particles of 50 μm exhibited lower TCE biodegradation efficiency due to particle aggregation, while particles of 2000 μm exhibited reduced efficiency due to lower specific surface area. This study moves a step for the in-situ microbial remediation of CEs-contaminated groundwater.