Systems metabolic engineering of Corynebacterium glutamicum for the efficient production of β-alanine

被引:0
|
作者
Ghiffary, Mohammad Rifqi [1 ,2 ]
Prabowo, Cindy Pricilia Surya [2 ,3 ]
Adidjaja, Joshua Julio [1 ,2 ]
Lee, Sang Yup [2 ,3 ,4 ]
Kim, Hyun Uk [1 ,2 ,4 ]
机构
[1] Systems Biology and Medicine Laboratory, Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon,34141, Korea, Republic of
[2] Systems Metabolic Engineering and Systems Healthcare Cross-Generation Collaborative Laboratory, KAIST, Daejeon,34141, Korea, Republic of
[3] Metabolic and Biomolecular Engineering National Research Laboratory, Department of Chemical and Biomolecular Engineering, KAIST Institute for BioCentury, KAIST, Daejeon,34141, Korea, Republic of
[4] BioProcess Engineering Research Center and BioInformatics Research Center, KAIST, Daejeon,34141, Korea, Republic of
来源
Metabolic Engineering | 2022年 / 74卷
基金
新加坡国家研究基金会;
关键词
Amino acids - Bacteriology - Biochemistry - Fermentation - Genes - Glucose - Metabolic engineering - Metabolism - Productivity - Strain;
D O I
暂无
中图分类号
学科分类号
摘要
β-Alanine is an important β-amino acid with a growing demand in a wide range of applications in chemical and food industries. However, current industrial production of β-alanine relies on chemical synthesis, which usually involves harmful raw materials and harsh production conditions. Thus, there has been increasing demand for more sustainable, yet efficient production process of β-alanine. In this study, we constructed Corynebacterium glutamicum strains for the highly efficient production of β-alanine through systems metabolic engineering. First, aspartate 1-decarboxylases (ADCs) from seven different bacteria were screened, and the Bacillus subtilis ADC showing the most efficient β-alanine biosynthesis was used to construct a β-alanine-producing base strain. Next, genome-scale metabolic simulations were conducted to optimize multiple metabolic pathways in the base strain, including phosphotransferase system (PTS)-independent glucose uptake system and the biosynthesis of key precursors, including oxaloacetate and L-aspartate. TCA cycle was further engineered for the streamlined supply of key precursors. Finally, a putative β-alanine exporter was newly identified, and its overexpression further improved the β-alanine production. Fed-batch fermentation of the final engineered strain BAL10 (pBA2_tr18) produced 166.6 g/L of β-alanine with the yield and productivity of 0.28 g/g glucose and 1.74 g/L/h, respectively. To our knowledge, this production performance corresponds to the highest titer, yield and productivity reported to date for the microbial fermentation. © 2022 International Metabolic Engineering Society
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页码:121 / 129
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