Metabolic engineering of <i>Escherichia coli</i> for the production of cadaverine: A five carbon diamine

TLDR

Cadaverine, a five‑carbon diamine, is a key platform chemical, and its bio‑based production from renewable feedstocks offers a sustainable alternative to petroleum‑derived synthesis. The study aimed to engineer an Escherichia coli strain capable of high‑yield cadaverine production in glucose mineral salts medium. Engineering involved disabling cadaverine degradation pathways, plasmid‑based overexpression of cadA under a tac promoter, and genomic replacement of the dapA promoter with a strong trc promoter to boost the lysine biosynthetic pool. The resulting strain produced 9.61 g L⁻¹ cadaverine with a productivity of 0.32 g L⁻¹ h⁻¹ in fed‑batch cultivation, demonstrating the strategy’s potential for renewable‑resource bio‑production.

Abstract

A five carbon linear chain diamine, cadaverine (1,5-diaminopentane), is an important platform chemical having many applications in chemical industry. Bio-based production of cadaverine from renewable feedstock is a promising and sustainable alternative to the petroleum-based chemical synthesis. Here, we report development of a metabolically engineered strain of Escherichia coli that overproduces cadaverine in glucose mineral salts medium. First, cadaverine degradation and utilization pathways were inactivated. Next, L-lysine decarboxylase, which converts L-lysine directly to cadaverine, was amplified by plasmid-based overexpression of the cadA gene under the strong tac promoter. Furthermore, the L-lysine biosynthetic pool was increased by the overexpression of the dapA gene encoding dihydrodipicolinate synthase through the replacement of the native promoter with the strong trc promoter in the genome. The final engineered strain was able to produce 9.61 g L(-1) of cadaverine with a productivity of 0.32 g L(-1) h(-1) by fed-batch cultivation. The strategy reported here should be useful for the bio-based production of cadaverine from renewable resources.