Disassembly and reassembly of polyhydroxyalkanoates: Recycling through abiotic depolymerization and biotic repolymerization

•Base depolymerizes polyhydroxyalkanoates (PHAs) to hydroxyacids and alkenoates.•Thermal treatment depolymerizes PHAs to alkenoates.•A microbial enrichment repolymerizes PHAs from hydroxyacids and alkenoates.•Nitrogen-limited cells produce high quality PHA homopolymer and copolymer.•Polyphosphate hydrolysis accompanies repolymerization.

An abiotic–biotic strategy for recycling of polyhydroxyalkanoates (PHAs) is evaluated. Base-catalyzed PHA depolymerization yields hydroxyacids, such as 3-hydroxybutyrate (3HB), and alkenoates, such as crotonate; catalytic thermal depolymerization yields alkenoates. Cyclic pulse addition of 3HB to triplicate bioreactors selected for an enrichment of Comamonas, Brachymonas and Acinetobacter. After each pulse, poly(3-hydroxybutyrate) (P3HB) transiently appeared: accumulation of P3HB correlated with hydrolysis of polyphosphate; consumption of P3HB correlated with polyphosphate synthesis. Cells removed from the cyclic regime and incubated with 3HB under nitrogen-limited conditions produced P3HB (molecular weight > 1,000,000 Da) at 50% of the cell dry weight (<8 h). P3HB also resulted from incubation with acetate, crotonate, or a mixture of hydrolytic depolymerization products. Poly(3-hydroxybutyric acid-co-3-hydroxyvaleric acid) (PHBV) resulted from incubation with valerate or 2-pentenoate. A recycling strategy where abiotic depolymerization of waste PHAs yields feedstock for customized PHA re-synthesis appears feasible, without the need for energy-intensive feedstock purification.