The search result changed since you submitted your search request. Documents might be displayed in a different sort order.
  • search hit 3 of 53
Back to Result List

Genetic analysis of the Bacillus licheniformis degSU operon and the impact of regulatory mutations on protease production

  • Disruption experiments targeted at the Bacillus licheniformis degSU operon and GFP-reporter analysis provided evidence for promoter activity immediately upstream of degU. pMutin mediated concomitant introduction of the degU32 allele – known to cause hypersecretion in Bacillus subtilis – resulted in a marked increase in protease activity. Application of 5-fluorouracil based counterselection through establishment of a phosphoribosyltransferase deficient Δupp strain eventually facilitated the marker-free introduction of degU32 leading to further protease enhancement achieving levels as for hypersecreting wild strains in which degU was overexpressed. Surprisingly, deletion of rapG – known to interfere with DegU DNA-binding in B. subtilis – did not enhance protease production neither in the wild type nor in the degU32 strain. The combination of degU32 and Δupp counterselection in the type strain is not only equally effective as in hypersecreting wild strains with respect to protease production but furthermore facilitates genetic strain improvement aiming at biological containment and effectiveness of biotechnological processes.

Export metadata

Additional Services

Share in Twitter Search Google Scholar
Metadaten
Author:Claudia Borgmeier, Johannes BongaertsORCiD, Friedhelm Meinhardt
DOI:https://doi.org/10.1016/j.jbiotec.2012.02.011
ISSN:1873-4863 (E-Journal); 0168-1656 (Print)
Parent Title (English):Journal of biotechnology
Publisher:Elsevier
Place of publication:Amsterdam
Document Type:Article
Language:English
Year of Completion:2012
Date of the Publication (Server):2013/11/20
Tag:Extracellular enzymes; Hypersecretion; Marker-free mutagenesis; Uracil-phosphoribosyltransferase
Volume:159
Issue:1-2
First Page:12
Last Page:20
Link:https://doi.org/10.1016/j.jbiotec.2012.02.011
Zugriffsart:campus
Institutes:FH Aachen / Fachbereich Chemie und Biotechnologie
FH Aachen / INB - Institut für Nano- und Biotechnologien
collections:Verlag / Elsevier