枯草芽孢杆菌
磷脂酸
生物合成
磷脂酶D
细胞外
生物化学
化学
细胞生物学
生物
细菌
酶
磷脂
遗传学
膜
作者
Peng Zhang,Xia Mao,Jin‐Song Gong,Xiaoli Kong,Chang Su,Xiaomei Zhang,Zhiming Rao,Zhenghong Xu,Jin‐Song Shi
标识
DOI:10.1016/j.biortech.2024.131492
摘要
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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