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Corynebacterium glutamicum is a key industrial workhorse for producing amino acids and high-value chemicals. Balancing metabolic flow between cell growth and product synthesis is crucial for enhancing production efficiency. Developing dynamic, broadly applicable, and minimally toxic gene regulation tools for C. glutamicum remains challenging, as optogenetic tools ideal for dynamic regulatory strategies have not yet been developed. This study introduces an advanced light-controlled gene expression system using light-controlled RNA-binding proteins (RBP), a first for Corynebacterium glutamicum. We established a gene expression regulation system, 'LightOnC.glu', utilizing the light-controlled RBP to construct light-controlled transcription factors in C. glutamicum. Simultaneously, we developed a high-performance light-controlled gene interference system using CRISPR/Cpf1 tools. The metabolic flow in the synthesis network was designed to enable the production of chitin oligosaccharides (CHOSs) and chondroitin sulphate oligosaccharides A (CSA) for the first time in C. glutamicum. Additionally, a light-controlled bioreactor was constructed, achieving a CHOSs production concentration of 6.2 g/L, the highest titer recorded for CHOSs biosynthesis to date. Herein, we have established a programmable light-responsive genetic circuit in C. glutamicum, advancing the theory of dynamic regulation based on light signaling. This breakthrough has potential applications in optimizing metabolic modules in other chassis cells and synthesizing other compounds.
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http://dx.doi.org/10.1093/nar/gkae1149 | DOI Listing |
Adv Biochem Eng Biotechnol
September 2025
Institute of Process Engineering in Life Sciences, Electrobiotechnology, Karlsruhe Institute of Technology, Karlsruhe, Germany.
While bioprocesses using Escherichia coli, Corynebacterium glutamicum, various species of Bacillus, lactic acid bacteria, Clostridia, the yeasts Saccharomyces cerevisiae and Pichia pastoris, fungi such as Aspergillus niger, and Chinese hamster ovary cells are well established, the high level of microbial diversity has not yet been exploited industrially. However, the use of alternative organisms has the potential to significantly expand the process window of bioprocesses. These extensions include the use of alternative substrates (e.
View Article and Find Full Text PDFInt J Biol Macromol
September 2025
Key Laboratory of Molecular Microbiology and Technology, Ministry of Education, College of Life Sciences, Nankai University, Tianjin, China. Electronic address:
Chondroitin sulfate (CS), a biopolymer with critical applications in osteoarthritis treatment and biomedical sectors, faces production challenges due to low yields and high costs. This study established a high-yield chondroitin (the major precursor of CS) production platform in Corynebacterium glutamicum for the simultaneous utilization of glucose and xylose from corn straw hydrolysate. Firstly, through codon optimization of genes encoding chondroitin synthase (KfoC) and UDP-N-acetylglucosamine-4-epimerase (KfoA), combined with tailoring metabolic pathways and medium components for chondroitin synthesis, yielded the high-titer strain CgC25.
View Article and Find Full Text PDFbioRxiv
August 2025
Institut Pasteur, Université Paris Cité, CNRS UMR 3528, Bacterial Cell Cycle Mechanisms Unit, F-75015 Paris, France.
Bacterial cell morphogenesis is controlled by the synthesis and organization of peptidoglycan and driven by multi-protein complexes such as the divisome and elongasome. Here we investigate the role of the DivIVA homologue, Wag31, the elongasome scaffold essential for polar growth in . Conditional depletion of Wag31 results in viable but coccoid-shaped cells, showing that Wag31 is essential for rod shape maintenance.
View Article and Find Full Text PDFSynth Syst Biotechnol
December 2025
School of Light Industry and Food Engineering, Guangxi University, 100 Daxue East Road, Nanning, Guangxi, 530004, China.
l-Homoserine is a valuable intermediate with broad applications in the food, pharmaceutical, and chemical industries. Although has been engineered for the efficient biosynthesis of l-homoserine, both production efficiency and glucose conversion remain suboptimal. In this study, an engineered strain capable of high-yield l-homoserine production from glucose was successfully developed.
View Article and Find Full Text PDFSynth Syst Biotechnol
December 2025
Key Laboratory of High Magnetic Field and Ion Beam Physical Biology, Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei, 230031, China.
Liquid-liquid phase separation (LLPS)-driven membraneless organelles (MLOs) have been employed to enhance metabolic efficiency in various microbial cell factories. However, their application in the industrial bacterium has not been explored. Here, we report the formation of liquid protein condensates in using the RGG domain of LAF-1.
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