Literature DB >> 1761510

A continuous cell-free protein synthesis system for coupled transcription-translation.

T Kigawa1, S Yokoyama.   

Abstract

A continuous cell-free protein synthesis system [Spirin et al. (1988) Science 242, 1162-1164] was modified so as to be suitable for coupled transcription-translation, a process useful for obtaining products of cloned genes or cDNAs. A reaction chamber equipped with an ultrafiltration membrane was newly designed and an HPLC pump was used to supply a low molecular weight substrate solution at a constant rate to the viscous reaction mixture in the chamber. By using an Escherichia coli S30 extract in this modified flow system (1 ml), coupled transcription-translation could be continuously performed for 17 h, the synthesized chloramphenicol acetyltransferase (congruent to 0.1 mg) being subsequently eluted through the chamber's membrane and then purified.

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Year:  1991        PMID: 1761510     DOI: 10.1093/oxfordjournals.jbchem.a123551

Source DB:  PubMed          Journal:  J Biochem        ISSN: 0021-924X            Impact factor:   3.387


  8 in total

1.  A highly efficient and robust cell-free protein synthesis system prepared from wheat embryos: plants apparently contain a suicide system directed at ribosomes.

Authors:  K Madin; T Sawasaki; T Ogasawara; Y Endo
Journal:  Proc Natl Acad Sci U S A       Date:  2000-01-18       Impact factor: 11.205

2.  Quantitation of protein expression in a cell-free system: Efficient detection of yields and 19F NMR to identify folded protein.

Authors:  Muniasamy Neerathilingam; Lesley H Greene; Simon A Colebrooke; Iain D Campbell; David Staunton
Journal:  J Biomol NMR       Date:  2005-01       Impact factor: 2.835

3.  Cell-free expression and stable isotope labelling strategies for membrane proteins.

Authors:  Solmaz Sobhanifar; Sina Reckel; Friederike Junge; Daniel Schwarz; Lei Kai; Mikhail Karbyshev; Frank Löhr; Frank Bernhard; Volker Dötsch
Journal:  J Biomol NMR       Date:  2009-08-13       Impact factor: 2.835

4.  Nuclease resistance of an extraordinarily thermostable mini-hairpin DNA fragment, d(GCGAAGC) and its application to in vitro protein synthesis.

Authors:  S Yoshizawa; T Ueda; Y Ishido; K Miura; K Watanabe; I Hirao
Journal:  Nucleic Acids Res       Date:  1994-06-25       Impact factor: 16.971

5.  Using an Escherichia coli cell-free extract to screen for soluble expression of recombinant proteins.

Authors:  Didier Busso; Rosalind Kim; Sung-Hou Kim
Journal:  J Struct Funct Genomics       Date:  2004

6.  Preparation of Escherichia coli cell extract for highly productive cell-free protein expression.

Authors:  Takanori Kigawa; Takashi Yabuki; Natsuko Matsuda; Takayoshi Matsuda; Rie Nakajima; Akiko Tanaka; Shigeyuki Yokoyama
Journal:  J Struct Funct Genomics       Date:  2004

7.  Cell-free synthesis and amino acid-selective stable isotope labeling of proteins for NMR analysis.

Authors:  T Kigawa; Y Muto; S Yokoyama
Journal:  J Biomol NMR       Date:  1995-09       Impact factor: 2.835

Review 8.  Engine out of the chassis: cell-free protein synthesis and its uses.

Authors:  Gabriel Rosenblum; Barry S Cooperman
Journal:  FEBS Lett       Date:  2013-10-22       Impact factor: 4.124

  8 in total

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