Please use this identifier to cite or link to this item: doi:10.22028/D291-48044
Title: Substrate-informed metabolic engineering of Corynebacterium glutamicum enables balanced glucose-xylose co-utilization for the valorization of lignocellulosic feedstocks
Author(s): Mees, David J.
Cao, Peng
Thönes, Ann-Kathrin
Ternes, Mario V.
Kohlstedt, Michael
Wittmann, Christoph
Language: English
Title: Metabolic Engineering
Volume: 95
Pages: 111-130
Publisher/Platform: Elsevier
Year of Publication: 2026
Free key words: Corynebacterium glutamicum
Metabolic engineering
Glucose–xylose co-utilization
13 C-tracer analysis
Carbon catabolite repression
Network flux integration
Cardboard hydrolysate
Lysine production
DDC notations: 500 Science
Publikation type: Journal Article
Abstract: Efficient co-utilization of glucose and xylose—the predominant sugars in lignocellulosic and paper-derived hydrolysates—remains a major bottleneck in microbial bioprocessing due to substrate hierarchy and carbon catabolite repression. Here, we develop a substrate-informed metabolic engineering framework in Corynebacte rium glutamicum that overcomes substrate hierarchy and carbon catabolite repression, enabling a balanced, largely transcription-independent glucose–xylose co-utilization regime at the level of central carbon metabolism. This regime is tailored to the sugar composition of cardboard hydrolysate (CBH), a waste-derived third-gener ation feedstock. A library of 34 engineered strains was constructed by systematically varying xylAB modules, transporter identity, promoter strength, and gene dosage. Integrated physiological, enzymatic, transcriptomic, and C-tracer analyses revealed strain XYL-6A as a representative of a distinct, kinetically balanced metabolic regime in which glucose- and xylose-derived fluxes merge early at the F6P/G3P node and maintain stable proportions independent of changing substrate levels or transcriptional adjustments. This regime arises from simple kinetic coordination of a compact, redox-neutral xylose-isomerase pathway with tuned transport capacity, eliminating the need for specialized feeding strategies, extensive regulatory rewiring, or attenuation of native glucose uptake. The optimized module translated directly into an industrial L-lysine producer, enabling high lysine yields from both defined mixtures and CBH (47.3 mmol C-mol 1 ). These results demonstrate how substrate-informed pathway design can exploit intrinsic network connectivity to achieve robust mixed-sugar metabolism. More broadly, they illustrate a core synthetic-biology principle: simple, well-balanced modules can generate scalable and reliable metabolic behaviors, providing a practical foundation for valorizing heterogeneous carbon feedstocks.
DOI of the first publication: 10.1016/j.ymben.2026.02.007
URL of the first publication: https://doi.org/10.1016/j.ymben.2026.02.007
Link to this record: urn:nbn:de:bsz:291--ds-480447
hdl:20.500.11880/42022
http://dx.doi.org/10.22028/D291-48044
ISSN: 1096-7184
1096-7176
Date of registration: 15-Jun-2026
Description of the related object: Supplementary data
Related object: https://ars.els-cdn.com/content/image/1-s2.0-S1096717626000261-mmc1.docx
Faculty: NT - Naturwissenschaftlich- Technische Fakultät
Department: NT - Biowissenschaften
Professorship: NT - Prof. Dr. Christoph Wittmann
Collections:SciDok - Der Wissenschaftsserver der Universität des Saarlandes

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