Engineering Microbes to Transform Waste into Wealth
Every minute, over 1 million plastic bottles are sold globally. Polyethylene terephthalate (PET)âthe lightweight, shatterproof polymer in these bottlesâaccounts for 12% of global solid waste. Less than 30% is recycled; the rest pollutes oceans, chokes landfills, and fragments into microplastics invading our food chain 1 5 . But what if we could turn this crisis into opportunity? Scientists are now engineering bacteria to "eat" PET waste and transform it into high-value productsâfrom biofuels to $7,500/kg carotenoids. This is bio-upcycling: nature's solution to humanity's plastic nightmare.
PET comprises two monomers: terephthalic acid (TPA) and ethylene glycol (EG). Traditional recycling has critical flaws:
In 2016, a breakthrough emerged: Ideonella sakaiensis, a bacterium that produces two enzymes:
These enzymes operate at ambient temperatures, slashing energy costs. But natural degradation is slow.
Scientists engineer enzymes for efficiency:
Modified LCC enzyme remains stable at:
Near PET's glass transition temperature for optimal degradation
Chimeric enzyme increases degradation:
Compared to natural enzyme systems
Once broken into TPA and EG, monomers feed engineered bacteria that convert waste into value:
Convert post-consumer PET into lycopeneâa high-value antioxidantâusing Rhodococcus jostii RPET without purifying monomers 5 6 .
Growth: RPET thrived in 0.6M TPA/EG mixâunlike model strains (e.g., E. coli) that require purified monomers 5 .
Lycopene Production: Engineered strains synthesized 1.3 mg/L lycopene directly from PET waste 6 .
Substrate | Growth Rate (hâ»Â¹) | TPA Utilization (%) |
---|---|---|
Purified TPA/EG | 0.22 | 100 |
Alkaline hydrolysate | 0.19 | 98 |
No carbon source | 0.01 | 0 |
Strain | Lycopene Yield (mg/L) | PET Conversion Efficiency (%) |
---|---|---|
Wild-type RPET | 0 | 0 |
Engineered RPET | 1.3 | 15.7 |
Engineered E. coli | 0.2 | <5 |
Reagent/Component | Function | Example/Commercial Source |
---|---|---|
PET hydrolases | Depolymerize PET into monomers | LCC variant (Carbios) 1 |
Alkaline hydrolysate | Crude TPA/EG mixture from PET hydrolysis | Lab-generated 6 |
Rhodococcus jostii RPET | Chassis for bioconversion | DSMZ culture collections |
Serine integrase (SIRT) | Chromosomal gene insertion | PhiC31 integrase 6 |
Ionic liquids | Depolymerize mixed PET/PLA plastics | [EMIM][OAc] 8 |
2-Methylhepta-3,5-diyn-2-ol | 3876-63-9 | C8H10O |
Recombinant Streptavidin-NC | Bench Chemicals | |
Recombinant Protein Cys-A/G | Bench Chemicals | |
(+)-Lactacystin Allyl Ester | C18H28N2O7S | |
9-(nitromethyl)-9H-fluorene | C14H11NO2 |
Pseudomonas putida strains engineered as "TPA specialists" and "EG specialists" work in tandem. This division of labor boosts substrate consumption by 104% versus monocultures 9 .
Engineering the β-hydroxyaspartate cycle (BHAC) from marine bacteria into P. putida improves EG assimilation efficiency by 35%, minimizing COâ loss .
Ionic liquids depolymerize mixed PET/PLA waste in one pot, enabling P. putida to convert it into PHA bioplasticsâcutting production costs by 62% 8 .
"Establishing sustainable material cycles is the greatest challenge of our time. Degrading plastics without COâ release closes the carbon loop."
With engineered consortia reaching TRL 4 6 , the path is clear: plastic waste is the next frontier for synthetic biologyâand our planet's lifeline.
Bio-upcycling transcends waste management. By transforming PET into performance-advantaged nylon, industrial pigments, or biodegradable polymers, it creates market incentives for reclamation. With engineered consortia reaching Technology Readiness Level (TRL) 4 6 , the path is clear: plastic waste is the next frontier for synthetic biologyâand our planet's lifeline.
Explore the BOTTLE Consortium's work on hybrid upcycling and CARBIOS' enzyme-enhanced recycling technology.