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Updated: Oct 25, 2026

Functional Complementation Analysis (FCA): A Laboratory Exercise Designed and Implemented to Supplement the Teaching of Biochemical Pathways
Published on: June 24, 2016
Enhanced d-Pantothenic Acid Biosynthesis in Corynebacterium glutamicum by the CPSPC System and Spatial Organization
Qing Yang1,2,3,4, Bo Zhang1,2,3,4, Lianggang Huang1,2,3,4
1State Key Laboratory of Green Chemical Synthesis and Conversion, Zhejiang University of Technology, Hangzhou310014, China.
Abstract:
d-Pantothenic acid (D-PA) is an essential precursor of coenzyme A and the acyl carrier protein. Its biosynthesis requires abundant precursors and precise regulation of the multifunctional enzyme, ketopantoate reductase. Here, we engineered Corynebacterium glutamicum for enhanced D-PA production through metabolic engineering, spatial enzyme organization, and a dynamically controlled CPSPC system (Coenzyme and Product Synthesis Pathway Coupling System). Competing pathways were suppressed, while target synthesis routes and 5,10-methylenetetrahydrofolate supply were strengthened. A RIAD-RIDD-mediated substrate channel between dihydroxy acid dehydratase and ketopantoate hydroxymethyltransferase was used to optimize enzymatic stoichiometry and localization. After functionalizing a glycine riboswitch in C. glutamicum, we developed the CPSPC system that dynamically couples one-carbon metabolism with D-PA synthesis. Fluorescence tracking confirmed its glycine-responsive regulation. The engineered strain DPAj-2-tuf achieved 23.06 g/L in a 5 L bioreactor over 63 h, productivity of 0.37 g/L/h, and glucose yield of 0.17 g/g. These outcomes offer an efficient and scalable strategy for industrial D-PA production using C. glutamicum.
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