@book{BergGaulHagedoornetal.1984, author = {Berg, G. and Gaul, G. and Hagedoorn, H. and Hardt, Arno and Heide, J. A. van der and Hinterberger, F. and Huber, Max and Jahn, R. and Martin, S. and Mayer-Kuckuk, T. and Osterfeld, F. and Paetz gen. Schieck, H. and Prasuhn, D. and Riepe, G. and Rogge, M. and Rossen, P. von and Schult, O. W. B. and Speth, J. and Turek, P.}, title = {Studie zum Bau eines kombinierten K{\"u}hler-Synchrotron-Rings an der KFA J{\"u}lich: COSY-Studie. Spezielle Berichte der Kernforschungsanlage J{\"u}lich. Nr. 0242. J{\"u}l-Spez-242}, publisher = {Kernforschungsanlage}, address = {J{\"u}lich}, pages = {65 S.}, year = {1984}, language = {de} } @inproceedings{MartinBergHardtetal.1979, author = {Martin, S. and Berg, G. and Hardt, Arno and H{\"u}rlimann, W. and K{\"o}hler, M. and Meißberger, J. and Sagefka, T. and Schult, O. W. B.}, title = {First experience with the magnet spectrometer 'BIG KARL'}, series = {Use of magnetic spectrometers in nuclear physics : proceedings of the Daresbury study weekend 10 - 11 March 1979}, booktitle = {Use of magnetic spectrometers in nuclear physics : proceedings of the Daresbury study weekend 10 - 11 March 1979}, editor = {Sanderson, N. E.}, publisher = {Daresbury Lab.}, address = {Daresbury}, pages = {38 -- 42}, year = {1979}, language = {en} } @article{RibitschHeumannKarletal.2012, author = {Ribitsch, D. and Heumann, S. and Karl, W. and Gerlach, J. and Leber, R. and Birner-Gruenberger, R. and Gruber, K. and Eiteljoerg, I. and Remler, P. and Siegert, Petra and Lange, J. and Maurer, Karl-Heinz and Berg, G. and Guebitz, G. M. and Schwab, H.}, title = {Extracellular serine proteases from Stenotrophomonas maltophilia: Screening, isolation and heterologous expression in E. coli}, series = {Journal of biotechnology}, volume = {157}, journal = {Journal of biotechnology}, number = {1}, publisher = {Elsevier}, address = {Amsterdam}, issn = {1873-4863 (E-Journal); 0168-1656 (Print)}, doi = {10.1016/j.jbiotec.2011.09.025}, pages = {140 -- 147}, year = {2012}, abstract = {A large strain collection comprising antagonistic bacteria was screened for novel detergent proteases. Several strains displayed protease activity on agar plates containing skim milk but were inactive in liquid media. Encapsulation of cells in alginate beads induced protease production. Stenotrophomonas maltophilia emerged as best performer under washing conditions. For identification of wash-active proteases, four extracellular serine proteases called StmPr1, StmPr2, StmPr3 and StmPr4 were cloned. StmPr2 and StmPr4 were sufficiently overexpressed in E. coli. Expression of StmPr1 and StmPr3 resulted in unprocessed, insoluble protein. Truncation of most of the C-terminal domain which has been identified by enzyme modeling succeeded in expression of soluble, active StmPr1 but failed in case of StmPr3. From laundry application tests StmPr2 turned out to be a highly wash-active protease at 45 °C. Specific activity of StmPr2 determined with suc-l-Ala-l-Ala-l-Pro-l-Phe-p-nitroanilide as the substrate was 17 ± 2 U/mg. In addition we determined the kinetic parameters and cleavage preferences of protease StmPr2.}, language = {en} }