A designed hybrid pathway for efficient synthesis of D-pantothenate in E. coli

D-Pantothenate (D-PA), a crucial precursor for coenzyme A, is widely used in various industries. Traditional chemical synthesis of D-PA involves toxic inputs, including cyanide, and generates environmental pollution. Total biosynthesis from glucose still has limitation in long reaction time and low titer. To provide a new approach to D-PA, we designed a hybrid pathway. First, we used green chemical method to convert inexpensive glyoxylate and isobutyaldehyde into 2-hydroxy-3-methyl-3-formylbutyric acid (HMFBA). Then we established a biosynthetic pathway to transform HMFBA into D-PA. Specifically, we engineered a malate dehydrogenase to achieve the efficient stereospecific conversion step. Optimization efforts led to a strain producing 116.5 g/L D-PA in 48 h, which is the highest rate and titier reported so far. This new approach offers a potentially economic and high-rate production route of D-PA.

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Publication Details

Journal
Metabolic Engineering
Published
2025-09-23
DOI
https://doi.org/10.1016/j.ymben.2025.09.007
Primary Topic
Neurological diseases and metabolism
Type
article
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A designed hybrid pathway for efficient synthesis of D-pantothenate in E. coli

Jing Zhao, Mengzhen Nie, Kechun Zhang, Yuchen Wang et al.
Metabolic Engineering
Neurological diseases and metabolism
article

A designed hybrid pathway for efficient synthesis of D-pantothenate in E. coli

Jing Zhao, Mengzhen Nie, Kechun Zhang, Yuchen Wang, Jilong Wang, Chenkai Cao
article en

Abstract

D-Pantothenate (D-PA), a crucial precursor for coenzyme A, is widely used in various industries. Traditional chemical synthesis of D-PA involves toxic inputs, including cyanide, and generates environmental pollution. Total biosynthesis from glucose still has limitation in long reaction time and low titer. To provide a new approach to D-PA, we designed a hybrid pathway. First, we used green chemical method to convert inexpensive glyoxylate and isobutyaldehyde into 2-hydroxy-3-methyl-3-formylbutyric acid (HMFBA). Then we established a biosynthetic pathway to transform HMFBA into D-PA. Specifically, we engineered a malate dehydrogenase to achieve the efficient stereospecific conversion step. Optimization efforts led to a strain producing 116.5 g/L D-PA in 48 h, which is the highest rate and titier reported so far. This new approach offers a potentially economic and high-rate production route of D-PA.

Metabolic EngineeringVol. 93
Westlake University (CN)
Openalex Percentile: Top 67%
Neurological diseases and metabolism
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