Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Laoshan District, Qingdao 266101, China.
Microb Cell Fact. 2012 May 20;11:65. doi: 10.1186/1475-2859-11-65.
With the increasing stress from oil price and environmental pollution, aroused attention has been paid to the microbial production of chemicals from renewable sources. The C12/14 and C16/18 alcohols are important feedstocks for the production of surfactants and detergents, which are widely used in the most respected consumer detergents, cleaning products and personal care products worldwide. Though bioproduction of fatty alcohols has been carried out in engineered E. coli, several key problems have not been solved in earlier studies, such as the quite low production of C16/18 alcohol, the lack of optimization of the fatty alcohol biosynthesis pathway, and the uncharacterized performance of the engineered strains in scaled-up system.
We improved the fatty alcohol production by systematically optimizing the fatty alcohol biosynthesis pathway, mainly targeting three key steps from fatty acyl-acyl carrier proteins (ACPs) to fatty alcohols, which are sequentially catalyzed by thioesterase, acyl-coenzyme A (CoA) synthase and fatty acyl-CoA reductase. By coexpression of thioesterase gene BTE, acyl-CoA synthase gene fadD and fatty acyl-CoA reductase gene acr1, 210.1 mg/L C12/14 alcohol was obtained. A further optimization of expression level of BTE, fadD and acr1 increased the C12/14 alcohol production to 449.2 mg/L, accounting for 75.0% of the total fatty alcohol production (598.6 mg/L). In addition, by coexpression of thioesterase gene 'tesA, acyl-CoA synthase gene fadD and fatty acyl-CoA reductase gene FAR, 101.5 mg/L C16/18 alcohol was obtained, with C16/18 alcohol accounting for 89.2% of the total fatty alcohol production.
To our knowledge, this is the first report on selective production of C12/14 and C16/18 alcohols by microbial fermentation. This work achieved high-specificity production of both C12/14 and C16/18 alcohols. The encouraging 598.6 mg/L of fatty alcohols represents the highest titer reported so far. In addition, the 101.5 mg/L 89.2% C16/18 alcohol suggests an important breakthrough in C16/18 alcohol production. A more detailed optimization of the expression level of fatty alcohol biosynthesis pathway may contribute to a further improvement of fatty alcohol production.
随着油价和环境污染压力的增加,人们对利用可再生资源通过微生物生产化学品的关注度日益提高。C12/14 和 C16/18 醇是生产表面活性剂和清洁剂的重要原料,广泛用于全球最受尊敬的消费清洁剂、清洁产品和个人护理产品。虽然已经在工程大肠杆菌中进行了脂肪酸醇的生物生产,但在早期研究中仍有几个关键问题尚未解决,例如 C16/18 醇的产量相当低、脂肪酸生物合成途径的优化不足以及工程菌株在扩大系统中的性能未得到充分表征。
我们通过系统优化脂肪酸醇生物合成途径来提高脂肪酸醇的产量,主要针对从脂肪酸酰基-酰基载体蛋白(ACP)到脂肪酸醇的三个关键步骤,这些步骤依次由硫酯酶、酰基辅酶 A(CoA)合成酶和脂肪酸酰基-CoA 还原酶催化。通过共表达硫酯酶基因 BTE、酰基辅酶 A 合成酶基因 fadD 和脂肪酸酰基-CoA 还原酶基因 acr1,获得了 210.1mg/L 的 C12/14 醇。进一步优化 BTE、fadD 和 acr1 的表达水平,将 C12/14 醇的产量提高到 449.2mg/L,占总脂肪酸醇产量(598.6mg/L)的 75.0%。此外,通过共表达硫酯酶基因'tesA、酰基辅酶 A 合成酶基因 fadD 和脂肪酸酰基-CoA 还原酶基因 FAR,获得了 101.5mg/L 的 C16/18 醇,C16/18 醇占总脂肪酸醇产量的 89.2%。
据我们所知,这是首次通过微生物发酵选择性生产 C12/14 和 C16/18 醇的报道。本工作实现了 C12/14 和 C16/18 醇的高特异性生产。令人鼓舞的 598.6mg/L 脂肪酸醇代表了迄今为止报道的最高浓度。此外,101.5mg/L 的 89.2% C16/18 醇表明在 C16/18 醇生产方面取得了重要突破。进一步优化脂肪酸醇生物合成途径的表达水平可能有助于进一步提高脂肪酸醇的产量。