Polyethylene terephthalate (PET) represents 8% of global solid waste. PET chemical recycling has been an option to solve this global problem, but it suffers from its relatively high process cost and the extremely low price of virgin PET. One solution to address this issue is to upcycle waste PET rather than recycle it to generate the same PET typically with low quality. PET upcycling can be achieved by depolymerizing PET into terephthalic acid (TPA) and ethylene glycol (EG) and biologically converting these monomers into value-added products. However, there are only a handful of reports demonstrating microbial strains capable of growing on both TPA and EG generated from PET as sole carbon sources. To overcome this critical limitation, we have performed strain screening to discover a <i>Rhodococcus </i>strain (named RPET) that can grow well on the alkaline hydrolysis products of PET as the sole carbon source without any purification step. Notably, this strain was able to tolerate and grow on a mixture of TPA and EG at extremely high concentrations (up to 0.3M each, total 0.6M) and high osmolarity resulting from alkaline hydrolysis and pH neutralization. The resultant pH neutralized media supported RPET’s growth (up to 0.4 g dry cell weight per g PET) without any purification and sterilization step except for their dilution to make up to 0.6M of monomer concentrations. In addition, many synthetic biology tools, developed for a related species <i>Rhodococcus opacus</i> (1), were functional in RPET, facilitating its engineering. In this presentation, we will discuss our effort to develop this novel chassis for waste PET valorization with PET conversion into carotenoids and muconate as two demonstration products (2).

Developing a novel microbial chassis for upcycling waste polyethylene terephthalate

ACS Fall 2021

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