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Titlebook: Recombinant Protein Production with Prokaryotic and Eukaryotic Cells. A Comparative View on Host Phy; Selected articles fr O.-W. Merten,D.

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书目名称Recombinant Protein Production with Prokaryotic and Eukaryotic Cells. A Comparative View on Host Phy
副标题Selected articles fr
编辑O.-W. Merten,D. Mattanovich,J. A. Cole
视频video
图书封面Titlebook: Recombinant Protein Production with Prokaryotic and Eukaryotic Cells. A Comparative View on Host Phy; Selected articles fr O.-W. Merten,D.
描述More then 20 years have passed now since the first recombinant protein producing microorganisms have been developed. In the meanwhile, numerous proteins have been produced in bacteria, yeasts and filamentous fungi, as weIl as higher eukaryotic cells, and even entire plants and animals. Many recombinant proteins are on the market today, and some of them reached substantial market volumes. On the first sight one would expect the technology - including the physiology of the host strains - to be optimised in detail after a 20 year‘s period of development. However, several constraints have limited the incentive for optimisation, especially in the pharmaceutical industry like the urge to proceed quickly or the requirement to define the production parameters for registration early in the development phase. The additional expenses for registration of a new production strain often prohibits a change to an optimised strain. A continuous optimisation of the entire production process is not feasible for the same reasons.
出版日期Book 2001
关键词Bur; Codons; DNA; Fermentation; Mammalia; Metabolism; Oxidation; Translation; biotechnology; development; gene
版次1
doihttps://doi.org/10.1007/978-94-015-9749-4
isbn_softcover978-90-481-5756-3
isbn_ebook978-94-015-9749-4
copyrightSpringer Science+Business Media Dordrecht 2001
The information of publication is updating

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Overexpression of a , Lipase in , Strains Containing Multiple Copies of the Target Geneons. The final . multicopy strains showed higher lipolytic activity and were isogenic with regard to the single copy . strain genetic background (i.e., His., Mut.), being therefore suitable for high density cultures using a defined synthetic medium.
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Development of a Heterologous Gene Expression System for Use in ,imately 300 mg of secreted protein per litre culture. We have successfully produced a number of heterologous proteins from both prokaryotic and eukaryotic organisms. The system is currently used for the production of bacterial vaccine components for use in humans.
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Expression and Fermentation Strategies for Recombinant Protein Production in , actual knowledge of the carbon flows, the energy situation, the activity of the protein synthesis apparatus, and the stress responses. Finally, various strategies are discussed to direct the recombinant protein to different cell compartments in order to improve the product yield or the yield of active protein.
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Protein Synthesis and Co-Translational Folding in Cell-Free Translation Systemsscription-translation systems are described. The continuous cell-free systems for gene expression are based on the use of a porous barrier that retains the high-molecular-weight components of the protein-synthesizing machinery within a defined reaction compartment, and at the same time provides the
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