Bornscheuer UT - Search Results

1

Discovery and Design of Family VIII Carboxylesterases as Highly Efficient Acyltransferases.

Müller H, Godehard SP, Palm GJ, Berndt L, Badenhorst CPS, Becker AK, Lammers M, Bornscheuer UT. Müller H, et al. Among authors: bornscheuer ut. Angew Chem Int Ed Engl. 2021 Jan 25;60(4):2013-2017. doi: 10.1002/anie.202014169. Epub 2020 Nov 23. Angew Chem Int Ed Engl. 2021. PMID: 33140887 Free PMC article.

2

Activity of lipases and esterases towards tertiary alcohols: insights into structure-function relationships.

Henke E, Pleiss J, Bornscheuer UT. Henke E, et al. Among authors: bornscheuer ut. Angew Chem Int Ed Engl. 2002 Sep 2;41(17):3211-3. doi: 10.1002/1521-3773(20020902)41:17<3211::AID-ANIE3211>3.0.CO;2-U. Angew Chem Int Ed Engl. 2002. PMID: 12207392 No abstract available.

3

Catalytic promiscuity in biocatalysis: using old enzymes to form new bonds and follow new pathways.

Bornscheuer UT, Kazlauskas RJ. Bornscheuer UT, et al. Angew Chem Int Ed Engl. 2004 Nov 19;43(45):6032-40. doi: 10.1002/anie.200460416. Angew Chem Int Ed Engl. 2004. PMID: 15523680

4

Kinetic resolution of 4-hydroxy-2-ketones catalyzed by a Baeyer-Villiger monooxygenase.

Kirschner A, Bornscheuer UT. Kirschner A, et al. Among authors: bornscheuer ut. Angew Chem Int Ed Engl. 2006 Oct 27;45(42):7004-6. doi: 10.1002/anie.200602986. Angew Chem Int Ed Engl. 2006. PMID: 17013956 No abstract available.

5

Isoenzymes of pig-liver esterase reveal striking differences in enantioselectivities.

Hummel A, Brüsehaber E, Böttcher D, Trauthwein H, Doderer K, Bornscheuer UT. Hummel A, et al. Among authors: bornscheuer ut. Angew Chem Int Ed Engl. 2007;46(44):8492-4. doi: 10.1002/anie.200703256. Angew Chem Int Ed Engl. 2007. PMID: 17902087 No abstract available.

6

Complete inversion of enantioselectivity towards acetylated tertiary alcohols by a double mutant of a Bacillus subtilis esterase.

Bartsch S, Kourist R, Bornscheuer UT. Bartsch S, et al. Among authors: bornscheuer ut. Angew Chem Int Ed Engl. 2008;47(8):1508-11. doi: 10.1002/anie.200704606. Angew Chem Int Ed Engl. 2008. PMID: 18203225 No abstract available.

7

A single residue influences the reaction mechanism of ammonia lyases and mutases.

Bartsch S, Bornscheuer UT. Bartsch S, et al. Among authors: bornscheuer ut. Angew Chem Int Ed Engl. 2009;48(18):3362-5. doi: 10.1002/anie.200900337. Angew Chem Int Ed Engl. 2009. PMID: 19343746

8

Converting an esterase into an epoxide hydrolase.

Jochens H, Stiba K, Savile C, Fujii R, Yu JG, Gerassenkov T, Kazlauskas RJ, Bornscheuer UT. Jochens H, et al. Among authors: bornscheuer ut. Angew Chem Int Ed Engl. 2009;48(19):3532-5. doi: 10.1002/anie.200806276. Angew Chem Int Ed Engl. 2009. PMID: 19350592

9

Exploiting the regioselectivity of Baeyer-Villiger monooxygenases for the formation of beta-amino acids and beta-amino alcohols.

Rehdorf J, Mihovilovic MD, Bornscheuer UT. Rehdorf J, et al. Among authors: bornscheuer ut. Angew Chem Int Ed Engl. 2010 Jun 14;49(26):4506-8. doi: 10.1002/anie.201000511. Angew Chem Int Ed Engl. 2010. PMID: 20455228 No abstract available.

10

The first artificial cell--a revolutionary step in synthetic biology?

Bornscheuer UT. Bornscheuer UT. Angew Chem Int Ed Engl. 2010 Jul 19;49(31):5228-30. doi: 10.1002/anie.201003393. Angew Chem Int Ed Engl. 2010. PMID: 20583024 No abstract available.

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