Affiliation:
1. 0000 0001 0708 1323 grid.258151.a Laboratory of Pharmaceutical Engineering, School of Pharmaceutics Science Jiangnan University Wuxi People’s Republic of China
2. 0000 0001 0708 1323 grid.258151.a National Engineering Laboratory for Cereal Fermentation Technology Jiangnan University 214122 Wuxi People’s Republic of China
3. 0000 0001 0708 1323 grid.258151.a The Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology Jiangnan University Wuxi People’s Republic of China
Abstract
Abstract
l-Serine is widely used in pharmaceutical, food and cosmetic industries, and the direct fermentation to produce l-serine from cheap carbon sources such as glycerol is greatly desired. The production of l-serine by engineered Escherichia coli from glycerol has not been achieved so far. In this study, E. coli was engineered to efficiently produce l-serine from glycerol. To this end, three l-serine deaminase genes were deleted in turn, and all of the deletions caused the maximal accumulation of l-serine at 0.06 g/L. Furthermore, removal of feedback inhibition by l-serine resulted in a titer of 1.1 g/L. Additionally, adaptive laboratory evolution was employed to improve glycerol utilization in combination with the overexpression of the cysteine/acetyl serine transporter gene eamA, leading to 2.36 g/L l-serine (23.6% of the theoretical yield). In 5-L bioreactor, l-serine titer could reach up to 7.53 g/L from glycerol, demonstrating the potential of the established strain and bioprocess.
Funder
National Natural Science Foundation of China
Natural Science Foundation of Jiangsu Province
Publisher
Oxford University Press (OUP)
Subject
Applied Microbiology and Biotechnology,Biotechnology,Bioengineering
Cited by
14 articles.
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