牛磺酸
谷氨酸棒杆菌
生物合成
生物化学
拉伤
化学
细菌
半胱氨酸
基因
代谢工程
氨基酸
生物
酶
遗传学
解剖
作者
Young‐Chul Joo,Young Jin Ko,Seung Kyou You,Sang Kyu Shin,Jeong Eun Hyeon,Almisned Shuaa Musaad,Sung Ok Han
标识
DOI:10.1021/acs.jafc.8b05093
摘要
Taurine is a biologically and physiologically valuable food additive. However, commercial taurine production mainly relies on environmentally harmful chemical synthesis. Herein, for the first time in bacteria, we attempted to produce taurine in metabolically engineered Corynebacterium glutamicum. The taurine-producing strain was developed by introducing cs, cdo1, and csad genes. Interestingly, while the control strain could not produce taurine, the engineered strains successfully produced taurine via the newly introduced metabolic pathway. Furthermore, we investigated the effect of a deletion strain of the transcriptional repressor McbR gene on taurine production. As a result, sulfur accumulation and l-cysteine biosynthesis were reinforced by the McbR deletion strain, which further increased the taurine production by 2.3-fold. Taurine production of the final engineered strain Tau11 was higher than in other previously reported strains. This study demonstrated a potential approach for eco-friendly biosynthesis as an alternative to the chemical synthesis of a food additive.
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