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Gene Review

ompT  -  outer membrane protease

Escherichia coli CFT073

 
 
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Disease relevance of ompT

  • Efficient presentation of the passenger domains was demonstrated in the outer membrane protease T-deficient (ompT) strain E. coli UT5600 and the ompT dsbA double mutant JK321 [1].
 

High impact information on ompT

  • Accordingly, we show that the presence of an F' episome results in increased resistance to the antimicrobial peptide protamine both in ompT mutants and in wild-type E. coli cells [2].
  • Here we report that SecY cleavage occurs even in cell extracts from ompT-disrupted cells, if they carry an F plasmid derivative [3].
  • To test the utility of this microarray device to detect genetically engineered bacteria, E. coli BL21 (a B strain derivative with antibiotic resistance gene, ampR) and E. coli JM107 (a K12 strain derivative lacking the gene ompT) were also employed [4].
  • After fusion to pelB, dsbA or ompT signal peptides no recombinant product could be obtained in the periplasm using the T7 promoter [5].

References

  1. Autodisplay: one-component system for efficient surface display and release of soluble recombinant proteins from Escherichia coli. Maurer, J., Jose, J., Meyer, T.F. J. Bacteriol. (1997) [Pubmed]
  2. Substrate Specificity of the Escherichia coli Outer Membrane Protease OmpP. Hwang, B.Y., Varadarajan, N., Li, H., Rodriguez, S., Iverson, B.L., Georgiou, G. J. Bacteriol. (2007) [Pubmed]
  3. The plasmid F OmpP protease, a homologue of OmpT, as a potential obstacle to E. coli-based protein production. Matsuo, E., Sampei, G., Mizobuchi, K., Ito, K. FEBS Lett. (1999) [Pubmed]
  4. DNA microarray for discrimination between pathogenic 0157:H7 EDL933 and non-pathogenic Escherichia coli strains. Wu, C.F., Valdes, J.J., Bentley, W.E., Sekowski, J.W. Biosensors & bioelectronics. (2003) [Pubmed]
  5. A novel fusion protein system for the production of native human pepsinogen in the bacterial periplasm. Malik, A., Rudolph, R., Söhling, B. Protein Expr. Purif. (2006) [Pubmed]
 
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