Substrate-informed metabolic engineering of Corynebacterium glutamicum enables balanced glucose–xylose co-utilization for the valorization of lignocellulosic feedstocks

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 Corynebacterium 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-generation 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 <sup>13</sup>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<sup>-1</sup>). 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.

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Journal
Metabolic Engineering
Published
2026-02-18
DOI
https://doi.org/10.1016/j.ymben.2026.02.007
Primary Topic
Microbial Metabolic Engineering and Bioproduction
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article
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article

Substrate-informed metabolic engineering of Corynebacterium glutamicum enables balanced glucose–xylose co-utilization for the valorization of lignocellulosic feedstocks

David Mees, Michael Kohlstedt, Christoph Wittmann, Peng Cao et al.
Metabolic Engineering
Microbial Metabolic Engineering and Bioproduction
article

Substrate-informed metabolic engineering of Corynebacterium glutamicum enables balanced glucose–xylose co-utilization for the valorization of lignocellulosic feedstocks

David Mees, Michael Kohlstedt, Christoph Wittmann, Peng Cao, Ann-Kathrin Thönes, Mario V. Ternes
article en

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 Corynebacterium 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-generation 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 <sup>13</sup>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<sup>-1</sup>). 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.

Metabolic EngineeringVol. 95
Saarland University (DE)
Openalex Percentile: Top 53%
Microbial Metabolic Engineering and Bioproduction
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