@article{SelmerBuckel1999, author = {Selmer, Thorsten and Buckel, Wolfgang}, title = {Oxygen Exchange between Acetate and the Catalytic Glutamate Residue in Glutaconate CoA-transferase from Acidaminococcus fermentans. IMPLICATIONS FOR THE MECHANISM OF CoA-ESTER HYDROLYSIS}, series = {Journal of Biological Chemistry. 274 (1999), H. 30}, journal = {Journal of Biological Chemistry. 274 (1999), H. 30}, isbn = {1083-351X}, pages = {20772 -- 20778}, year = {1999}, language = {en} } @article{UndenBeckerBongaertsetal.1994, author = {Unden, G. and Becker, S. and Bongaerts, Johannes and Schirawski, J. and Six, S.}, title = {Oxygen regulated gene expression in facultatively anaerobic bacteria}, series = {Antonie van Leeuwenhoek}, volume = {Vol. 66}, journal = {Antonie van Leeuwenhoek}, number = {Iss. 1-3}, issn = {0003-6072 (Print) ; 1572-9699 (online)}, pages = {3 -- 22}, year = {1994}, language = {en} } @article{BiselliBornWandrey1995, author = {Biselli, Manfred and Born, C. and Wandrey, C.}, title = {Oxygen transfer from the gasphase to the immobilized cells in membrane aerated fluidized beds / Born, C. ; Biselli, M. ; Wandrey, C.}, series = {Animal cell technology : basic \& applied aspects : proceedings of the Eighth Annual Meeting of the Japanese Association for Animal Cell Technology, Iizuka, Fukuoka, Japan, November 6-10, 1995 / edited by K. Funatsu, Y. Shirai, and T. Matsushita}, journal = {Animal cell technology : basic \& applied aspects : proceedings of the Eighth Annual Meeting of the Japanese Association for Animal Cell Technology, Iizuka, Fukuoka, Japan, November 6-10, 1995 / edited by K. Funatsu, Y. Shirai, and T. Matsushita}, publisher = {Kluwer Acad. Press}, address = {Boston}, isbn = {0-7923-4486-3}, pages = {83 -- 87}, year = {1995}, language = {en} } @article{SelmerAndrei2001, author = {Selmer, Thorsten and Andrei, Paula I.}, title = {p-Hydroxyphenylacetate decarboxylase from Clostridium difficile. A novel glycyl radical enzyme catalysing the formation of p-cresol}, series = {European Journal of Biochemistry. 268 (2001), H. 5}, journal = {European Journal of Biochemistry. 268 (2001), H. 5}, isbn = {0014-2956}, pages = {1363 -- 1372}, year = {2001}, language = {en} } @article{TippkoetterRoikaewUlberetal.2010, author = {Tippk{\"o}tter, Nils and Roikaew, Wipa and Ulber, Roland and Hoffmann, Alexander and Denzler, Hans-J{\"o}rg and Buchholz, Heinrich}, title = {Paracoccus denitrificans for the effluent recycling during continuous denitrification of liquid food}, series = {Biotechnology Progress}, volume = {26}, journal = {Biotechnology Progress}, number = {3}, publisher = {Wiley}, address = {Hoboken, NJ}, issn = {8756-7938}, doi = {10.1002/btpr.384}, pages = {756 -- 762}, year = {2010}, abstract = {Nitrate is an undesirable component of several foods. A typical case of contamination with high nitrate contents is whey concentrate, containing nitrate in concentrations up to 25 l. The microbiological removal of nitrate by Paracoccus denitrificans under formation of harmless nitrogen in combination with a cell retention reactor is described here. Focus lies on the resource-conserving design of a microbal denitrification process. Two methods are compared. The application of polyvinyl alcohol-immobilized cells, which can be applied several times in whey feed, is compared with the implementation of a two step denitrification system. First, the whey concentrate's nitrate is removed by ion exchange and subsequently the eluent regenerated by microorganisms under their retention by crossflow filtration. Nitrite and nitrate concentrations were determined by reflectometric color measurement with a commercially available Reflectoquant® device. Correction factors for these media had to be determined. During the pilot development, bioreactors from 4 to 250 mg·L-1 and crossflow units with membrane areas from 0.02 to 0.80 m2 were examined. Based on the results of the pilot plants, a scaling for the exemplary process of denitrifying 1,000 tons per day is discussed.}, language = {en} } @article{KotterLiRiekert1990, author = {Kotter, Michael and Li, D. X. and Riekert, Lothar}, title = {Partial oxidation of o-xylene to phthalic anhydride in a structured fixed bed containing a sequence of catalysts}, series = {New developments in selective oxidation : proceedings of an international symposium ; Rimini, Italy, Sept. 18 - 22, 1989 / eds.: G. Centi ... - (Studies in surface science and catalysis ; 55)}, journal = {New developments in selective oxidation : proceedings of an international symposium ; Rimini, Italy, Sept. 18 - 22, 1989 / eds.: G. Centi ... - (Studies in surface science and catalysis ; 55)}, publisher = {Elsevier}, address = {Amsterdam}, isbn = {0-444-88694-X}, pages = {267 -- 274}, year = {1990}, language = {en} } @article{KotterXingLi1990, author = {Kotter, Michael and Xing Li, Dong}, title = {Partielle Oxidation von o-Xylol zu Phthals{\"a}reanhydrid an V/Ti-Schalenkatalysatoren : [Synopsis 1898]}, series = {Chemie - Ingenieur - Technik. 62 (1990), H. 11}, journal = {Chemie - Ingenieur - Technik. 62 (1990), H. 11}, isbn = {0009-286X}, pages = {950 -- 951}, year = {1990}, language = {de} } @article{KotterLiRiekert1991, author = {Kotter, Michael and Li, D. X. and Riekert, Lothar}, title = {Partielle Oxidation von o-Xylol zu Phthals{\"a}ureanhydrid in einem strukturierten Festbettreaktor}, series = {Katalyse : katalytische Abgasreinigung, Zeolithe, homogene Katalyse, selektive Reaktionen, Herstellung und Charakterisierung, Ionenleiter, Elektrokatalyse, SLPC-Katalysatoren, Suspensionsphase ; Vortr{\"a}ge von der DECHEMA-Jahrestagung 1990, 31. Mai und 1. Juni 1990 / hrsg. von H. Kral. - (Deutsche Gesellschaft f{\"u}r Chemisches Apparatewesen, Chemische Technik und Biotechnologie: DECHEMA-Monographien ; 122)}, journal = {Katalyse : katalytische Abgasreinigung, Zeolithe, homogene Katalyse, selektive Reaktionen, Herstellung und Charakterisierung, Ionenleiter, Elektrokatalyse, SLPC-Katalysatoren, Suspensionsphase ; Vortr{\"a}ge von der DECHEMA-Jahrestagung 1990, 31. Mai und 1. Juni 1990 / hrsg. von H. Kral. - (Deutsche Gesellschaft f{\"u}r Chemisches Apparatewesen, Chemische Technik und Biotechnologie: DECHEMA-Monographien ; 122)}, publisher = {VCH}, address = {Weinheim}, isbn = {3-527-10216-7}, pages = {93 -- 123}, year = {1991}, language = {de} } @article{SchwertnerBerndtGielenetal.1975, author = {Schwertner, Eberhard and Berndt, Heinz and Gielen, Hans-G{\"u}nter and Zahn, Helmut}, title = {Peptide 96 : Synthese einiger [2-(p-Biphenylyl)isopropyloxycarbonyl]-Aminos{\"a}urederivate}, series = {Justus Liebigs Annalen der Chemie}, volume = {75}, journal = {Justus Liebigs Annalen der Chemie}, number = {3}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {1099-0690}, doi = {10.1002/jlac.197519750318}, pages = {581 -- 585}, year = {1975}, abstract = {Die Darstellung der N-[2-(p-Biphenylyl)isopropyloxycarbonyl]-Derivate (Bpoc-Derivate) des Cysteins unter Verwendung der Thiolschutzgruppen Tetrahydropyranyl (Thp) f{\"u}r 1, Diphenylmethyl (Dpm) f{\"u}r 2, Trityl (Trt) f{\"u}r 3 und S-tert.-Butyl (SBut) f{\"u}r 4 sowie die Synthese von aktivierten Estern der Bpoc-Derivate des Glycins (5), Isoleucins (6) und Prolins (7) werden beschrieben. An einem Beispiel wird die M{\"o}glichkeit aufgezeigt, die Bpoc-Gruppe {\"u}ber das Bpoc-Azid nachtr{\"a}glich in den Peptidverband einzuf{\"u}hren.}, language = {de} } @article{BerndtZahn1975, author = {Berndt, Heinz and Zahn, Helmut}, title = {Peptide, 99 : Monomere cyclische Cystinpeptidderivate, III ; Synthese der Schafinsulin-A-Kettensequenzen A2-21 und A1-21 als monomere cyclische Dicystinpeptidderivate}, series = {Justus Liebigs Annalen der Chemie}, volume = {1975}, journal = {Justus Liebigs Annalen der Chemie}, number = {9}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {1099-0690}, doi = {10.1002/jlac.197519750908}, pages = {1601 -- 1612}, year = {1975}, abstract = {Die Synthese der Sequenzen A2—21 (13) und A1—21 (15) der Schafinsulin-A-Kette als monomere cyclische Dicystinpeptidderivate wird beschrieben. Die intrachenaren Cystinbr{\"u}cken A6—7 und A 11 —20 vermitteln die L{\"o}slichkeit dieser Derivate in Dimethylformamid und erm{\"o}glichen erstmalig die Reindarstellung vollgesch{\"u}tzter Insulin-A-Kettenderivate. Die w{\"a}hrend der Synthese eingesetzten Schutzgruppen lassen sich mittels Trifluoressigs{\"a}ure und 2-Mercapto{\"a}thanol quantitativ entfernen.}, language = {de} }