Metabolic engineering of Escherichia coli for the biosynthesis of nylon 6 and nylon 6,6 monomers

Hexamethylenediamine (HMD), adipic acid, and ε-caprolactam (ε-CL) are essential C6 monomers used in the production of nylon 6,6 and nylon 6. Developing sustainable, bio-based routes to these compounds remains challenging due to pathway complexity. Here, we report a modular Escherichia coli platform for the de novo biosynthesis of all three monomers directly from glycerol. We divided the overall pathway into upstream and downstream modules, with the upstream module converting glycerol to adipic acid. To construct downstream module, two distinct strains were engineered to individually convert adipic acid into HMD or ε-CL. Both strains employed carboxylic acid reductases Macar from Mycobacteroides abscessus and Mmocar from Mycolicibacterium moriokaense , with the latter identified and validated in this work. Specifically, HMD biosynthesis incorporated aminotransferases PatA from E. coli , GabT from Streptomyces avermitilis , and the introduced Bcta from Burkholderia cenocepacia . ε-CL biosynthesis utilized a similar upstream pathway but relied critically on a lactamization step catalyzed by an HLadh–Smnox fusion enzyme containing a flexible linker for efficient NAD + regeneration. The common precursor, adipic acid, was produced by an upstream strain optimized through reverse β-oxidation pathway reconstruction, PaaJ engineering, and metabolic flux balancing, achieving a titer of 6.1 g/L. In fed-batch fermentation, cocultivation of the engineered strains with delayed inoculation enabled temporally coordinated conversion of glycerol to HMD (230.9 mg/L) and ε-CL (808.0 µg/L), representing low yet the highest titers reported to date. This work opens up the possibility of a unified, modular microbial platform for the sustainable production of nylon monomers from a renewable carbon source.