Acetol biosynthesis enables NADPH balance during nitrogen limitation in engineered Escherichia coli

被引:0
作者
Sudarsan, Suresh [2 ]
Demling, Philipp [1 ]
Ozdemir, Emre [2 ]
Ben Ammar, Aziz [1 ]
Mennicken, Philip [1 ]
Buescher, Joerg M. [3 ,4 ]
Meurer, Guido [3 ]
Ebert, Birgitta E. [5 ]
Blank, Lars M. [1 ]
机构
[1] Rhein Westfal TH Aachen, Inst Appl Microbiol IAMB, Aachen Biol & Biotechnol ABBt, D-52074 Aachen, Germany
[2] Tech Univ Denmark, Novo Nord Fdn Ctr Biosustainabil, Kemitorvet 220, DK-2800 Lyngby, Denmark
[3] BRAIN Biotech AG, D-64673 Zwingenberg, Germany
[4] Max Planck Inst Immunobiol & Epigenet, D-79108 Freiburg, Germany
[5] Univ Queensland, Australian Inst Bioengn & Nanotechnol, St Lucia, Qld 4072, Australia
关键词
Metabolic engineering; C-13 metabolic flux analysis; Glycerol; Acetol; Escherichia coli; Cofactor generation; ADAPTIVE EVOLUTION; STATIONARY-PHASE; GLYCEROL KINASE; CARBON SOURCE; FLUX; METHYLGLYOXAL; MEVALONATE; METABOLISM; GROWTH; GENES;
D O I
10.1186/s12934-025-02687-z
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background Nutrient limitation strategies are commonly applied in bioprocess development to engineered microorganisms to further maximize the production of the target molecule towards theoretical limits. Biomass formation is often limited under the limitation of key nutrients, and understanding how fluxes in central carbon metabolism are re-routed during the transition from nutrient excess to nutrient-limited condition is vital to target and tailor metabolic engineering strategies. Here, we report the physiology and intracellular flux distribution of an engineered acetol-producing Escherichia coli on glycerol under nitrogen-limited, non-growing production conditions. Results Acetol production in the engineered E. coli strain is triggered upon nitrogen depletion. During nitrogen limitation, glycerol uptake decreased, and biomass formation rates ceased. We applied C-13-flux analysis with 2-C-13 glycerol during exponential growth and nitrogen starvation to elucidate flux re-routing in the central carbon metabolism. The results indicate a metabolically active non-growing state with significant flux re-routing towards acetol biosynthesis and reduced flux through the central carbon metabolism. The acetol biosynthesis pathway is favorable for maintaining the NADPH/NADP(+) balance. Conclusion The results reported in this study illustrate how the production of a value-added chemical from a waste stream can be connected to the metabolism of the whole-cell biocatalyst, making product formation mandatory for the cell to maintain its NADPH/NADP(+) balance. This has implications for process design and further metabolic engineering of the whole-cell biocatalyst.
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页数:12
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共 65 条
[1]   Enhanced production of (R)-1,8-propanediol by metabolically engineered Escherichia coli [J].
Altaras, NE ;
Cameron, DC .
BIOTECHNOLOGY PROGRESS, 2000, 16 (06) :940-946
[2]  
AMBUDKAR SV, 1986, J BIOL CHEM, V261, P9083
[3]   Absolute metabolite concentrations and implied enzyme active site occupancy in Escherichia coli [J].
Bennett, Bryson D. ;
Kimball, Elizabeth H. ;
Gao, Melissa ;
Osterhout, Robin ;
Van Dien, Stephen J. ;
Rabinowitz, Joshua D. .
NATURE CHEMICAL BIOLOGY, 2009, 5 (08) :593-599
[4]   Enabling anaerobic growth of Escherichia coli on glycerol in defined minimal medium using acetate as redox sink [J].
Boecker, Simon ;
Espinel-Rios, Sebastian ;
Bettenbrock, Katja ;
Klamt, Steffen .
METABOLIC ENGINEERING, 2022, 73 :50-57
[5]   Increasing ATP turnover boosts productivity of 2,3-butanediol synthesis in Escherichia coli [J].
Boecker, Simon ;
Harder, Bjoern-Johannes ;
Kutscha, Regina ;
Pfluegl, Stefan ;
Klamt, Steffen .
MICROBIAL CELL FACTORIES, 2021, 20 (01)
[6]   A NOVEL FERMENTATION - THE PRODUCTION OF R(-)-1,2-PROPANEDIOL AND ACETOL BY CLOSTRIDIUM-THERMOSACCHAROLYTICUM [J].
CAMERON, DC ;
COONEY, CL .
BIO-TECHNOLOGY, 1986, 4 (07) :651-654
[7]   Structural basis of the redox switch in the OxyR transcription factor [J].
Choi, HJ ;
Kim, SJ ;
Mukhopadhyay, P ;
Cho, S ;
Woo, JR ;
Storz, G ;
Ryu, SE .
CELL, 2001, 105 (01) :103-113
[8]   The commercial production of chemicals using pathway engineering [J].
Chotani, G ;
Dodge, T ;
Hsu, A ;
Kumar, M ;
LaDuca, R ;
Trimbur, D ;
Weyler, W ;
Sanford, K .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY, 2000, 1543 (02) :434-455
[9]   Environmental Dependence of Stationary-Phase Metabolism in Bacillus subtilis and Escherichia coli [J].
Chubukov, Victor ;
Sauer, Uwe .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2014, 80 (09) :2901-2909
[10]   Understanding the glycerol market [J].
Ciriminna, Rosaria ;
Della Pina, Cristina ;
Rossi, Michele ;
Pagliaro, Mario .
EUROPEAN JOURNAL OF LIPID SCIENCE AND TECHNOLOGY, 2014, 116 (10) :1432-1439