High-level extracellular expression of phospholipase D by combinatorial fine-tuning strategy in Bacillus subtilis for efficient biosynthesis of phosphatidic acid

Although Bacillus subtilis shows promise as a potential microbial cell factory for phospholipase D (PLD) expression, its production capacity remains insufficient. In this study, a secretory expression system, by co-optimization the promoter and signal peptides and employing a fed-batch fermentation strategy, was constructed to enhance expression of PLD from separate sources. The highest PLD production of 4056.9 U/mL was observed using this system, with a PLD production efficiency of 52.0 U/mL/h. Finally, a phosphatidic acid (PA) biosynthesis system was established using the constructed PLD as a catalyst, which achieved a PA yield of 219.1 g/L. This is the highest PLD production and PA yield reported globally to date. The protocol has significant potential for application for industrial PLD production as well as enzymatic phospholipids modification and also provides a valuable reference for overexpressing proteins in B. subtilis.

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Publication Details

Journal
Bioresource Technology
Published
2024-09-27
DOI
https://doi.org/10.1016/j.biortech.2024.131492
Citations
4
Primary Topic
Enzyme Catalysis and Immobilization
Type
article
Field-Weighted Citation Impact
0.94

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article

High-level extracellular expression of phospholipase D by combinatorial fine-tuning strategy in Bacillus subtilis for efficient biosynthesis of phosphatidic acid

Jin‐Song Gong, Jin‐Song Shi, Xiaoli Kong, Zhenghong Xu et al.
4 citations
Bioresource Technology
Enzyme Catalysis and Immobilization
0.94
article

High-level extracellular expression of phospholipase D by combinatorial fine-tuning strategy in Bacillus subtilis for efficient biosynthesis of phosphatidic acid

Jin‐Song Gong, Jin‐Song Shi, Xiaoli Kong, Zhenghong Xu, Zhiming Rao, Chang Su, Xiaomei Zhang, Peng Zhang, Xin-An Mao
article en
4 citations

Abstract

Although Bacillus subtilis shows promise as a potential microbial cell factory for phospholipase D (PLD) expression, its production capacity remains insufficient. In this study, a secretory expression system, by co-optimization the promoter and signal peptides and employing a fed-batch fermentation strategy, was constructed to enhance expression of PLD from separate sources. The highest PLD production of 4056.9 U/mL was observed using this system, with a PLD production efficiency of 52.0 U/mL/h. Finally, a phosphatidic acid (PA) biosynthesis system was established using the constructed PLD as a catalyst, which achieved a PA yield of 219.1 g/L. This is the highest PLD production and PA yield reported globally to date. The protocol has significant potential for application for industrial PLD production as well as enzymatic phospholipids modification and also provides a valuable reference for overexpressing proteins in B. subtilis.

Bioresource TechnologyVol. 414
Jiangnan University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Jiangsu Province, Taishan Industry Leading Talents, Fundamental Research Funds for the Central Universities, National Key Research and Development Program of China Stem Cell and Translational Research
Zero hunger
Openalex Percentile: Top 25%
Enzyme Catalysis and Immobilization
0.94
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