Stereospecific Enzymatic Transformation of α-Ketoglutarate to (2S,3R)-3-Methyl Glutamate during Acidic Lipopeptide Biosynthesis-Reference-Cited by-同舟云学术

Stereospecific Enzymatic Transformation of α-Ketoglutarate to (2S,3R)-3-Methyl Glutamate during Acidic Lipopeptide Biosynthesis

Published:2007-09-05 Issue:39 Volume:129 Page:12011-12018
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Mahlert Christoph¹,Kopp Florian¹,Thirlway Jenny¹,Micklefield Jason¹,Marahiel Mohamed A.¹

Affiliation:

1. Contribution from the Fachbereich Chemie/Biochemie, Philipps-Universität Marburg, Hans-Meerwein-Strasse D-35032 Marburg, Germany, and School of Chemistry & Manchester Interdisciplinary Biocentre, The University of Manchester, 131 Princess Street, Manchester, M1 7DN, United Kingdom

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja074427i

Reference38 articles.

1. Polyketide and Nonribosomal Peptide Antibiotics: Modularity and Versatility

2. Molecular Mechanisms Underlying Nonribosomal Peptide Synthesis: Approaches to New Antibiotics

3. Biosynthesis of Nonribosomal Peptides

4. Tailoring enzymes that modify nonribosomal peptides during and after chain elongation on NRPS assembly lines

5. From The Cover: SyrB2 in syringomycin E biosynthesis is a nonheme FeII -ketoglutarate- and O2-dependent halogenase

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