Zobrazeno 1 - 10
of 94
pro vyhledávání: '"Kerstin Steiner"'
Autor:
Birgit Grill, Maximilian Glänzer, Helmut Schwab, Kerstin Steiner, Daniel Pienaar, Dean Brady, Kai Donsbach, Margit Winkler
Publikováno v:
Molecules, Vol 25, Iss 11, p 2521 (2020)
Nitrile hydratases (NHase) catalyze the hydration of nitriles to the corresponding amides. We report on the heterologous expression of various nitrile hydratases. Some of these enzymes have been investigated by others and us before, but sixteen targe
Externí odkaz:
https://doaj.org/article/3a759537ed4c491084b2d8b1d422c684
Autor:
Dominik M. Müller, Kerstin Steiner
Publikováno v:
Journal of Current Southeast Asian Affairs, Vol 37 (2018)
Externí odkaz:
https://doaj.org/article/5820443e85254c2e85b76a300d4daf25
Autor:
Kerstin Steiner
Publikováno v:
Journal of Current Southeast Asian Affairs, Vol 37 (2018)
Islam plays a pivotal political role in Southeast Asian countries, where the governments that have ruled since independence have been concerned with influencing the trajectory, content, hermeneutic and style of the legal traditions of their Muslim ci
Externí odkaz:
https://doaj.org/article/5096cb082a074a4f913e8aeb2a1abba5
Autor:
Tea Pavkov-Keller, Kerstin Steiner, Mario Faber, Martin Tengg, Helmut Schwab, Mandana Gruber-Khadjawi, Karl Gruber
Publikováno v:
PLoS ONE, Vol 12, Iss 2, p e0171056 (2017)
Friedel-Crafts alkylation of aromatic systems is a classic reaction in organic chemistry, for which regiospecific mono-alkylation, however, is generally difficult to achieve. In nature, methyltransferases catalyze the addition of methyl groups to a w
Externí odkaz:
https://doaj.org/article/9fad6ec7b63d4975b0e90a7b5e97f40b
Publikováno v:
Computational and Structural Biotechnology Journal, Vol 10, Iss 16, Pp 58-62 (2014)
Hydroxynitrile lyases (HNLs) are powerful carbon–carbon bond forming enzymes. The reverse of their natural reaction – the stereoselective addition of hydrogen cyanide (HCN) to carbonyls – yields chiral cyanohydrins, versatile building blocks fo
Externí odkaz:
https://doaj.org/article/810ee9088aa546be957f0eb23a1a6d0d
Publikováno v:
Frontiers in Microbiology, Vol 7 (2016)
Oxidative cleavage of alkenes is a widely employed process allowing oxyfunctionalization to corresponding carbonyl compounds. Recently, a novel biocatalytic oxidative alkene cleavage activity on styrene derivatives was identified in TM1459 from Therm
Externí odkaz:
https://doaj.org/article/52b4ca1b7c8f4a7086af151f3d1e48c1
Autor:
Andrzej Łyskowski, Christian Gruber, Georg Steinkellner, Martin Schürmann, Helmut Schwab, Karl Gruber, Kerstin Steiner
Publikováno v:
PLoS ONE, Vol 9, Iss 1, p e87350 (2014)
Chiral amines are important building blocks for the synthesis of pharmaceutical products, fine chemicals, and agrochemicals. ω-Transaminases are able to directly synthesize enantiopure chiral amines by catalysing the transfer of an amino group from
Externí odkaz:
https://doaj.org/article/d97d7bbb595e42e8a46ceea7ad294efa
Autor:
Kerstin Steiner, Helmut Schwab
Publikováno v:
Computational and Structural Biotechnology Journal, Vol 2, Iss 3, p e201209010 (2012)
Enzymes are an attractive alternative in the asymmetric syntheses of chiral building blocks. To meet the requirements of industrial biotechnology and to introduce new functionalities, the enzymes need to be optimized by protein engineering. This arti
Externí odkaz:
https://doaj.org/article/05a932f5dc674f82bd54dc55e1526021
Autor:
Robin Ristl, Kerstin Steiner, Kristof Zarschler, Sonja Zayni, Paul Messner, Christina Schäffer
Publikováno v:
International Journal of Microbiology, Vol 2011 (2011)
The amazing repertoire of glycoconjugates present on bacterial cell surfaces includes lipopolysaccharides, capsular polysaccharides, lipooligosaccharides, exopolysaccharides, and glycoproteins. While the former are constituents of Gram-negative cells
Externí odkaz:
https://doaj.org/article/02a6f6f41444483ca643979573e8b1b2
Publikováno v:
Organic Process Research & Development. 26:2102-2110
Ene reductases catalyze the biocatalytic reduction of activated alkenes, offering a powerful biobased alternative to metal-catalyzed and organocatalyzed double-bond reductions. With the aim to utilize the natural catalysts for the development of sust
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85fd90e72d9850ff71f0a8f813b9c920
https://doi.org/10.1021/acs.oprd.2c00096
https://doi.org/10.1021/acs.oprd.2c00096