Home > Publications database > Metabolic engineering of Corynebacterium glutamicum for production of scyllo-inositol, a drug candidate against Alzheimer's disease > print |
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100 | 1 | _ | |a Ramp, Paul |0 P:(DE-Juel1)176186 |b 0 |
245 | _ | _ | |a Metabolic engineering of Corynebacterium glutamicum for production of scyllo-inositol, a drug candidate against Alzheimer's disease |
260 | _ | _ | |a Orlando, Fla. |c 2021 |b Academic Press |
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520 | _ | _ | |a Scyllo-inositol has been identified as a potential drug for the treatment of Alzheimer's disease. Therefore, cost-efficient processes for the production of this compound are desirable. In this study, we analyzed and engineered Corynebacterium glutamicum with the aim to develop competitive scyllo-inositol producer strains. Initial studies revealed that C. glutamicum naturally produces scyllo-inositol when cultured with myo-inositol as carbon source. The conversion involves NAD+-dependent oxidation of myo-inositol to 2-keto-myo-inositol followed by NADPH-dependent reduction to scyllo-inositol. Use of myo-inositol for biomass formation was prevented by deletion of a cluster of 16 genes involved in myo-inositol catabolism (strain MB001(DE3)Δiol1). Deletion of a second cluster of four genes (oxiC-cg3390-oxiD-oxiE) related to inositol metabolism prevented conversion of 2-keto-myo-inositol to undesired products causing brown coloration (strain MB001(DE3)Δiol1Δiol2). The two chassis strains were used for plasmid-based overproduction of myo-inositol dehydrogenase (IolG) and scyllo-inositol dehydrogenase (IolW). In BHI medium containing glucose and myo-inositol, a complete conversion of the consumed myo-inositol into scyllo-inositol was achieved with the Δiol1Δiol2 strain. To enable scyllo-inositol production from cheap carbon sources, myo-inositol 1-phosphate synthase (Ino1) and myo-inositol 1-phosphatase (ImpA), which convert glucose 6-phosphate into myo-inositol, were overproduced in addition to IolG and IolW using plasmid pSI. Strain MB001(DE3)Δiol1Δiol2 (pSI) produced 1.8 g/L scyllo-inositol from 20 g/L glucose and even 4.4 g/L scyllo-inositol from 20 g/L sucrose within 72 h. Our results demonstrate that C. glutamicum is an attractive host for the biotechnological production of scyllo-inositol and potentially further myo-inositol-derived products. |
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700 | 1 | _ | |a Lehnert, Alexander |0 P:(DE-Juel1)180545 |b 1 |
700 | 1 | _ | |a Matamouros, Susana |0 P:(DE-Juel1)165848 |b 2 |
700 | 1 | _ | |a Wirtz, Astrid |0 P:(DE-Juel1)171825 |b 3 |
700 | 1 | _ | |a Baumgart, Meike |0 P:(DE-Juel1)145489 |b 4 |
700 | 1 | _ | |a Bott, Michael |0 P:(DE-Juel1)128943 |b 5 |e Corresponding author |
773 | _ | _ | |a 10.1016/j.ymben.2021.06.011 |g Vol. 67, p. 173 - 185 |0 PERI:(DE-600)1471017-1 |p 173 - 185 |t Metabolic engineering |v 67 |y 2021 |x 1096-7176 |
856 | 4 | _ | |u https://juser.fz-juelich.de/record/894472/files/Ramp%20et%20al%202021%20R1.pdf |y Published on 2021-09-01. Available in OpenAccess from 2022-09-01. |z StatID:(DE-HGF)0510 |
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