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PMID: 16534780 Published · ppublish English Comparative Study Journal Article Research Support, N.I.H., Extramural

A tightly regulated inducible expression system utilizing the fim inversion recombination switch.

Biotechnology and bioengineering ·Vol. 94 ·No. 1 ·2006-05-05 ·Pages 1-4

Ham TS, Lee SK, Keasling JD, Arkin AP

Abstract

The fim inversion system of Escherichia coli (E. coli) can behave as a unidirectional switch in an efficient manner. We have developed a new expression system for E. coli, comprising the arabinose-inducible fimE gene and the fim invertible DNA segment containing a constitutively active promoter. In this system, the target gene is cloned with the promoter in the OFF orientation, resulting in no transcribed product. When induced by arabinose, the active promoter is switched to the ON orientation via FimE-catalyzed DNA inversion, and the gene is expressed. Our expression system exhibited very tightly controlled basal expression and high induced expression, with simple induction by inexpensive arabinose. These characteristics make our system suitable for large-scale expression or for production of toxic proteins.

MeSH Terms
Chromosome Inversion Escherichia coli/genetics,growth & development Fimbriae Proteins/genetics Gene Expression Regulation, Bacterial Genes, Bacterial Genes, Switch Promoter Regions, Genetic Recombination, Genetic
Chemicals
Fimbriae Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Ham Timothy S
Department of Bioengineering, University of California, Berkeley, 94720, USA.
Lee Sung Kuk
Keasling Jay D
Arkin Adam P
Article Info
Journal
Biotechnology and bioengineering
Abbr.
Biotechnol Bioeng
ISSN
0006-3592
Published
2006-05-05
Pages
1-4
Language
English
Region
United States
NLM ID
7502021
Subset
IM
Grants
NIGMS NIH HHS · 5R01GM063525-03 · United States
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