Engineering precursor and co-factor supply to enhance D-pantothenic acid production in Bacillus megaterium

High-yielding chemical and chemo-enzymatic methods of D-pantothenic acid (DPA) synthesis are limited by using poisonous chemicals and DL-pantolactone racemic mixture formation. Alternatively, the safe microbial fermentative route of DPA production was found promising but suffered from low productivity and precursor supplementation. In this study, Bacillus megaterium was metabolically engineered to produce DPA without precursor supplementation. In order to provide a higher supply of precursor D-pantoic acid, key genes involved in its synthesis are overexpressed, resulting strain was produced 0.53 +/- 0.08 g/L DPA was attained in shake flasks. Cofactor CH2-THF was found to be vital for DPA biosynthesis and was regenerated through the serine-glycine degradation pathway. Enhanced supply of another precursor, beta-alanine was achieved by codon optimization and dosing of the limiting L-asparate- 1-decarboxylase (ADC). Co-expression of Pantoate-beta-alanine ligase, ADC, phosphoenolpyruvate carboxylase, aspartate aminotransferase and aspartate ammonia-lyase enhanced DPA concentration to 2.56 +/- 0.05 g/L at shake flasks level. Fed-batch fermentation in a bioreactor with and without the supplementation of p-alanine increased DPA concentration to 19.52 +/- 0.26 and 4.78 +/- 0.53 g/L, respectively. This present study successfully demonstrated a rational approach combining precursor supply engineering with cofactor regeneration for the enhancement of DPA titer in recombinant B. megaterium.

Automated summary

This study successfully improved the production of DPA using metabolic engineering and synthetic biology approaches, achieving higher DPA concentration without precursor supplementation. By overexpressing genes involved in DPA synthesis and optimizing precursor supply, significant enhancement of DPA concentration was achieved.