Engineering Triggers Glutamic Acid Accumulation in Biotin-rich Corn Stover Hydrolysate
Overview
Authors
Affiliations
Background: Lignocellulose biomass contains high amount of biotin and resulted in an excessive biotin condition for cellulosic glutamic acid accumulation by . Penicillin or ethambutol triggers cellulosic glutamic acid accumulation, but they are not suitable for practical use due to the fermentation instability and environmental concerns. Efficient glutamic acid production from lignocellulose feedstocks should be achieved without any chemical inductions.
Results: An industrial strain S9114 was metabolically engineered to achieve efficient glutamic acid accumulation in biotin-excessive corn stover hydrolysate. Among the multiple metabolic engineering efforts, two pathway regulations effectively triggered the glutamic acid accumulation in lignocellulose hydrolysate. The C-terminal truncation of glutamate secretion channel MscCG (ΔC110) led to the successful glutamic acid secretion in corn stover hydrolysate without inductions. Then the α-oxoglutarate dehydrogenase complex (ODHC) activity was attenuated by regulating RBS sequence, and glutamic acid accumulation was further elevated for more than fivefolds. The obtained XW6 strain reached a record-high titer of 65.2 g/L with the overall yield of 0.63 g/g glucose using corn stover as the starting feedstock without any chemical induction.
Conclusions: Metabolic engineering method was successfully applied to achieve efficient glutamic acid in biotin-rich lignocellulose hydrolysate for the first time. This study demonstrated the high potential of glutamic acid production from lignocellulose feedstock.
Rapid screening of point mutations by mismatch amplification mutation assay PCR.
Zhang F, Liu Z, Liu S, Zhang W, Wang B, Li C Appl Microbiol Biotechnol. 2024; 108(1):190.
PMID: 38305911 PMC: 10837254. DOI: 10.1007/s00253-024-13036-2.
Microbial membrane transport proteins and their biotechnological applications.
Ozkan M, Yilmaz H, Ergenekon P, Erdogan E, Erbakan M World J Microbiol Biotechnol. 2024; 40(2):71.
PMID: 38225445 PMC: 10789880. DOI: 10.1007/s11274-024-03891-6.
Jungmann L, Hoffmann S, Lang C, De Agazio R, Becker J, Kohlstedt M Microb Cell Fact. 2022; 21(1):274.
PMID: 36578077 PMC: 9798599. DOI: 10.1186/s12934-022-02003-z.
Ujor V, Okonkwo C Front Bioeng Biotechnol. 2022; 10:1061667.
PMID: 36483774 PMC: 9723337. DOI: 10.3389/fbioe.2022.1061667.
Xu Y, Hua K, Huang Z, Zhou P, Wen J, Jin C Biotechnol Biofuels Bioprod. 2022; 15(1):29.
PMID: 35292099 PMC: 8922798. DOI: 10.1186/s13068-022-02129-7.