Difficult-to-remove microplastic pollution poses serious
risks
to ecosystems and human health. Sewage treatment plants also cannot
remove microplastics completely with filters or harsh chemical treatments.
It is imperative to develop biotechnologies that aggregate microplastics
into larger sizes for rapid removal from polluted waters. Using experimental
evolution, we generated microplastic aggregators (MAGs) from the environmentally
prevalent Pseudomonas aeruginosa, which are evolved
to aggregate microplastics into sizable aggregates via biofilm formation.
This is mediated by upregulation of a cyclic-di-GMP (c-di-GMP) secondary
messenger signaling system found in most bacterial species. Comparative
genomic analysis of MAGs revealed mutations in the yfiR gene, which is the repressor of tpbB, a c-di-GMP
synthesizing diguanylate cyclase (DGC). Derepression of tpbB conferred MAGs with high intracellular c-di-GMP content and production
of a CdrA biofilm matrix protein, resulting in higher biofilm formation
and aggregation of microplastics with various sizes and materials.
To release microplastics from the aggregates for downstream resource
recovery, we employed protease (trypsin) to degrade CdrA and disrupt
the biofilm matrix. As a proof-of-concept method, we demonstrated
that a capture-then-release approach could mitigate microplastic pollution
in seawater samples collected in the vicinity of a sewage outfall.
Hence, our work provides insights into efficient biological removal
of other micropollutants or biofilm-enabled catalysis of microparticles.