Full-text resources of PSJD and other databases are now available in the new Library of Science.
Visit https://bibliotekanauki.pl

PL EN


Preferences help
enabled [disable] Abstract
Number of results
2007 | 54 | 3 | 671-672

Article title

A freeze-thaw method for disintegration of Escherichia coli cells producing T7 lysozyme used in pBAD expression systems

Content

Title variants

Languages of publication

EN

Abstracts

EN
The pLysN plasmid containing the T7 lysozyme gene under control of the lac promoter was constructed to facilitate cell disintegration after expression of recombinant proteins in arabinose-induced expression systems. The usefulness of this plasmid was tested in Escherichia coli TOP10 and E. coli LMG194 cells carrying pBADMHADgeSSB plasmid containing Deinococcus geothermalis SSB protein gene under control of the araBAD promoter. The results showed that low-level expression of T7 lysozyme did not interfere with the target SSB protein production, and that the freezing-thawing treatment was sufficient for disruption of the E. coli cells producing low amounts of T7 lysozyme.

Year

Volume

54

Issue

3

Pages

671-672

Physical description

Dates

published
2007
received
2007-08-08
revised
2007-09-10
accepted
2007-09-14
(unknown)
2007-09-17

Contributors

  • Department of Microbiology, Chemical Faculty, Gdańsk University of Technology, Gdańsk, Poland
  • Department of Microbiology, Chemical Faculty, Gdańsk University of Technology, Gdańsk, Poland
author
  • Department of Microbiology, Chemical Faculty, Gdańsk University of Technology, Gdańsk, Poland

References

  • Bollag DM, Rozycki MD, Edelstein SJ (1996) In Protein Methods, pp 27-43. Wiley-Liss Inc., New York.
  • Filipkowski P, Duraj-Thatte A, Kur J (2006) Arch Microbiol 186: 129-137.
  • Studier FW (1991) J Mol Biol 219: 37-44.

Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.bwnjournal-article-abpv54p671kz
JavaScript is turned off in your web browser. Turn it on to take full advantage of this site, then refresh the page.