4.6 Article

Metabolic Engineering of Corynebacterium glutamicum for Sustainable Production of the Aromatic Dicarboxylic Acid Dipicolinic Acid

Journal

MICROORGANISMS
Volume 10, Issue 4, Pages -

Publisher

MDPI
DOI: 10.3390/microorganisms10040730

Keywords

dipicolinic acid; Corynebacterium glutamicum; metabolic engineering; sustainable production; nonsterile fermentation; phosphite

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Funding

  1. BMBF [031B0825C]

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DPA is a heat-stable and easily biodegradable compound that has the potential to replace fossil-based plastics and has pharmaceutical applications. This study successfully achieved de novo production of DPA in C. glutamicum by overexpressing related genes and explored the utilization of different carbon sources and non-sterile conditions for DPA production.
Dipicolinic acid (DPA) is an aromatic dicarboxylic acid that mediates heat-stability and is easily biodegradable and non-toxic. Currently, the production of DPA is fossil-based, but bioproduction of DPA may help to replace fossil-based plastics as it can be used for the production of polyesters or polyamides. Moreover, it serves as a stabilizer for peroxides or organic materials. The antioxidative, antimicrobial and antifungal effects of DPA make it interesting for pharmaceutical applications. In nature, DPA is essential for sporulation of Bacillus and Clostridium species, and its biosynthesis shares the first three reactions with the L-lysine pathway. Corynebacterium glutamicum is a major host for the fermentative production of amino acids, including the million-ton per year production of L-lysine. This study revealed that DPA reduced the growth rate of C. glutamicum to half-maximal at about 1.6 g center dot L-1. The first de novo production of DPA by C. glutamicum was established by overexpression of dipicolinate synthase genes from Paenibacillus sonchi genomovar riograndensis SBR5 in a C. glutamicum L-lysine producer strain. Upon systems metabolic engineering, DPA production to 2.5 g center dot L-1 in shake-flask and 1.5 g center dot L-1 in fed-batch bioreactor cultivations was shown. Moreover, DPA production from the alternative carbon substrates arabinose, xylose, glycerol, and starch was established. Finally, expression of the codon-harmonized phosphite dehydrogenase gene from P. stutzeri enabled phosphite-dependent non-sterile DPA production.

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