Background
To simplify the use of minimal medium, Scarab Genomics offers a three component kit consisting of 10X Modified Korz Medium with separate 50X Magnesium Sulfate and 50% Glucose solutions. The concentrated minimal medium and associated Magnesium Sulfate and Glucose solutions are diluted to create a 1X medium. The diluted 1X medium containing Magnesium Sulfate and 0.2% glucose (and appropriate antibiotics) is used for expression optimization in shake flasks. The same medium (supplemented with additional glucose to a final concentration of 0.5% and additional phosphate buffer) also serves as the “batch” phase medium in fed-batch fermentations. Scarab’s Clean Genome® strains were specifically designed for the production of biotherapeutic protein and DNA. The “cleanest” medium to use for biotherapeutic production is a chemically defined, minimal medium. Accordingly, Modified Korz Minimal Medium has been extensively tested with the Scarab Clean Genome® Strains to verify its ability to support cell growth and the production of recombinant protein. Korz minimal medium was originally designed for high density fed-batch fermentation of E. coli (Korz et al. 1995). The medium consists of phosphate buffer, magnesium, ferric citrate, trace elements, and uses glucose as the carbon source. The same base medium used for optimizing expression in shake flasks can also be used for fed-batch fermentation, thereby providing continuity between the two processes. In fed-batch fermentations, the same medium is supplemented with higher glucose and phosphate buffer content. A separate Korz Feed Medium (Cat. No. D-0710-1L5) supplies glucose, magnesium, iron, and trace elements for the feeding stage of fed-batch fermentation.
Specifications
Kit Components
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10X Modified Korz Medium | 100 ml (D-0710-100) | 1000 ml (D-0710-1L) |
50X Magnesium Sulfate | 20 ml (D-0710-100M) | 200 ml (D-0710-1LM) |
50% Glucose | 4 ml (D0710-100G) | 40 ml (D-0710-1LG) |
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Support
Product Manuals 10X Modified Korz Medium with Glucose Kit Papers
- Korz DJ, Rinas U, Hellmuth K, Sanders EA, Deckwer WD. J Biotechnol. (1995) Feb 21;39(1):59-65. Simple fed-batch technique for high cell density cultivation of Escherichia coli.
- Pósfai G, et al., (2006) Emergent properties of reduced-genome Escherichia coli. Science 312:1044-6.
Patents & Disclaimers
Products are sold for non-commercial use only, under Scarab Genomics limited use label license: Limited Label Use.Scarab is providing you with this Material subject to the non-transferable right to use the subject amount of the Material for your research at your academic institution. The Recipient agrees not to sell or otherwise transfer this Material, or anything derived or produced from the Material to a third party. NO RIGHTS ARE PROVIDED TO USE THE MATERIAL OR ANYTHING DERIVED OR PRODUCED FROM THE MATERIAL FOR COMMERCIAL PURPOSES. If the Recipient makes any changes to the chromosome of the Material that results in an invention in breach of this limited license, then Scarab will have a worldwide, exclusive, royalty-free license to such invention whether patentable or not. If the Recipient is not willing to accept the terms of this limited license, Scarab is willing to accept return of this product with a full refund, minus shipping and handling costs. For information on obtaining a license to this Material for purposes other than research, please contact Scarab’s Licensing Department. Scarab Genomics’ technology is covered by U.S. Pat. No. 6,989,265 and related foreign applications. Clean Genome® is a registered trademark of Scarab Genomics, LLC.