Literature DB >> 19003413

Regulated multicistronic expression technology for mammalian metabolic engineering.

M Fussenegger1, S Moser, J E Bailey.   

Abstract

Contemporary basic research is rapidly revealing increasingly complex molecular regulatory networks which are often interconnected via key signal integrators. These connections among regulatory and catalytic networks often frustrate bioengineers as promising metabolic engineering strategies are bypassed by compensatory metabolic responses or cause unexpected, undesired outcomes such as apoptosis, product protein degradation or inappropriate post- translational modification. Therefore, for metabolic engineering to achieve greater success in mammalian cell culture processes and to become important for future applications such as gene therapy and tissue engineering, this technology must be enhanced to allow simultaneous, in cases conditional, reshaping of metabolic pathways to access difficult-to-attain cell states. Recent advances in this new territory of multigene metabolic engineering are intimately linked to the development of multicistronic expression technology which allows the simultaneous, and in some cases, regulated expression of several genes in mammalian cells. Here we review recent achievements in multicistronic expression technology in view of multigene metabolic engineering.

Entities:  

Year:  1998        PMID: 19003413      PMCID: PMC3449837          DOI: 10.1023/A:1008037916674

Source DB:  PubMed          Journal:  Cytotechnology        ISSN: 0920-9069            Impact factor:   2.058


  117 in total

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Journal:  Biotechnol Prog       Date:  1998 Sep-Oct

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Authors:  E T Papoutsakis
Journal:  Nat Biotechnol       Date:  1998-05       Impact factor: 54.908

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Authors:  A Hoffmann; M Villalba; L Journot; D Spengler
Journal:  Nucleic Acids Res       Date:  1997-03-01       Impact factor: 16.971

6.  Design of a novel bicistronic expression vector with demonstration of a p16INK4-induced G(1)-S block(1).

Authors:  N E Poulos; A A Farmer; K W Chan; E J Stanbridge
Journal:  Cancer Res       Date:  1996-04-15       Impact factor: 12.701

7.  Translation of human hepatitis C virus RNA in cultured cells is mediated by an internal ribosome-binding mechanism.

Authors:  C Wang; P Sarnow; A Siddiqui
Journal:  J Virol       Date:  1993-06       Impact factor: 5.103

8.  Autoregulated multicistronic expression vectors provide one-step cloning of regulated product gene expression in mammalian cells.

Authors:  M Fussenegger; S Moser; X Mazur; J E Bailey
Journal:  Biotechnol Prog       Date:  1997 Nov-Dec

9.  Construction of adenoviral and retroviral vectors coexpressing the genes encoding the hepatitis B surface antigen and B7-1 protein.

Authors:  X S He; M Rivkina; W S Robinson
Journal:  Gene       Date:  1996-10-10       Impact factor: 3.688

10.  Specific loss of apoptotic but not cell-cycle arrest function in a human tumor derived p53 mutant.

Authors:  S Rowan; R L Ludwig; Y Haupt; S Bates; X Lu; M Oren; K H Vousden
Journal:  EMBO J       Date:  1996-02-15       Impact factor: 11.598

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  3 in total

Review 1.  Creating biological nanomaterials using synthetic biology.

Authors:  MaryJoe K Rice; Warren C Ruder
Journal:  Sci Technol Adv Mater       Date:  2013-12-03       Impact factor: 8.090

2.  Engineering Synthetic Chromosomes by Sequential Loading of Multiple Genomic Payloads over 100 Kilobase Pairs in Size.

Authors:  Amy Greene; Kara Pascarelli; Dominique Broccoli; Edward Perkins
Journal:  Mol Ther Methods Clin Dev       Date:  2019-04-29       Impact factor: 6.698

3.  An internal ribosome entry site (IRES) mutant library for tuning expression level of multiple genes in mammalian cells.

Authors:  Esther Y C Koh; Steven C L Ho; Zhiwei Song; Xuezhi Bi; Muriel Bardor; Yuansheng Yang
Journal:  PLoS One       Date:  2013-12-09       Impact factor: 3.240

  3 in total

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