Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Hans-Heinrich Förster"'
Autor:
Heike Schürer, Günter Mayer, Hans-Heinrich Förster, Peter Welzel, Dietmar Knoll, Michael Blind, Michael Famulok, Ulrich Hahn, Katherina Stembera
Publikováno v:
Bioorganic & Medicinal Chemistry. 9:2557-2563
Nuclease-resistant moenomycin-binding aptamers with dissociation constants in the range of 300 to 400 nM have been selected. Competition experiments have demonstrated that these aptamers recognize a disaccharide analogue of moenomycin. The results of
Publikováno v:
Biochemical and Biophysical Research Communications. 286:652-658
CYP153 a cytochrome P450 from Acinetobacter sp. EB104 catalyzes the hydroxylation of unsubstituted n -alkanes. We have decided to use the CYP153 system as a model for mechanistic studies on regioselective n -alkane oxidation and the interaction of hy
Publikováno v:
Nucleosides and Nucleotides. 16:727-732
In this work the expression of functional ribonuclease T1 on the surface of the filamentous Escherichia coli phage M13 is described. Ribonuclease T1 was fused to the phage coat protein pIII and functionally displayed on the phage surface as shown by
Autor:
Ulrich Hahn, Hans-Heinrich Förster, Stefan Vogel, Peter Welzel, Marc Struhalla, Heike Betat, Michael Famulok
Publikováno v:
Biological chemistry. 384(10-11)
Moenomycin A is an amphiphilic phosphoglycolipid antibiotic that interferes with the transglycosylation step in peptidoglycan biosynthesis. The antibiotic consists of a branched pentasaccharide moiety, connected to the moenocinol lipid via a glycerop
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 207
Publikováno v:
Biological chemistry. 382(7)
An RNA sequence showing high stability with respect to digestion by ribonuclease T1 (RNase T1) was isolated by in vitro selection from an RNA library. Although ribonuclease T1 cleaves single-stranded RNA specifically after guanosine residues, seconda
Publikováno v:
The Journal of investigative dermatology. 100(6)
To appreciate point mutations in keratin genes as causes for hereditary epithelial diseases, the normal variation of these gene sequences in the population must be known. Because genetic polymorphism of keratins at the protein level due to allelic va