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Functional diversity in gentisate 1,2 dioxygenases: A spectroscopic study

R. Gupta, E. Eppinger, J. Gröning, and A. Stolz. 255th National Meeting and Exposition of the American-Chemical-Society (ACS), 255, Washington, DC, American Chemical Society, (2018)

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apl. Prof. Dr. Andreas Stolz University of Stuttgart

Katharina Stolz University of Stuttgart

Dennis Stolze University of Stuttgart

Merlin Stölzle University of Stuttgart

Prof. Dr. Andreas Hotho

Ontology-based Text Document Clustering.A. Hotho, A. Maedche, and S. Staab. KI, 16 (4): 48-54 (2002)

Ontology-based Text Document Clustering.A. Hotho, A. Maedche, and S. Staab. KI, 16 (4): 48-54 (2002)Clustern mit Hintergrundwissen.A. Hotho. Karlsruhe Institute of Technology, (2004)

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High strength bio-concrete for the production of building componentsM. Smirnova, C. Nething, A. Stolz, J. Gröning, D. Funaro, E. Eppinger, M. Reichert, J. Frick, and L. Blandini. npj Materials Sustainability, 1 (1): 4 (2023)Expansion of the substrate range of the gentisate 1,2-dioxygenase from Corynebacterium glutamicum for the conversion of monohydroxylated benzoatesE. Eppinger, and A. Stolz. Protein engineering design & selection, 30 (1): 57-65 (2017)Comparative Analysis of the Conversion of Mandelonitrile and 2-Phenylpropionitrile by a Large Set of Variants Generated from a Nitrilase Originating from Pseudomonas fluorescens EBC191A. Stolz, E. Eppinger, O. Sosedov, and C. Kiziak. Molecules, 24 (23): 4232 (2019)Conversion of aliphatic nitriles by the arylacetonitrilase from Pseudomonas fluorescens EBC191S. Brunner, E. Eppinger, S. Fischer, J. Gröning, and A. Stolz. World journal of microbiology & biotechnology, 34 (7): 91 (2018)Crystal structure of the monocupin ring-cleaving dioxygenase 5-nitrosalicylate 1,2-dioxygenase from Bradyrhizobium sp.E. Eppinger, A. Stolz, and M. Ferraroni. Acta crystallographica. Section D, Structural biology, 79 (7): 632-640 (2023)Chemoenzymatic enantioselective synthesis of phenylglycine and phenylglycine amide by direct coupling of the Strecker synthesis with a nitrilase reactionE. Eppinger, J. Gröning, and A. Stolz. Frontiers in catalysis, (2022)Spontaneous release of fluoride during the dioxygenolytic cleavage of 5-fluorosalicylate by the salicylate 1,2-dioxygenase from Pseudaminobacter salicylatoxidans BN12E. Eppinger, S. Bürger, and A. Stolz. FEMS microbiology letters, 363 (1): fnv211 (2016)Conversion of phenylglycinonitrile by recombinant Escherichia coli cells synthesizing variants of the arylacetonitrilase from Pseudomonas fluorescens EBC191E. Eppinger, and A. Stolz. Applied Microbiology and Biotechnology, 103 (16): 6737-6746 (2019)Function of different amino acid residues in the reaction mechanism of gentisate 1,2-dioxygenases deduced from the analysis of mutants of the salicylate 1,2-dioxygenase from Pseudaminobacter salicylatoxidansE. Eppinger, M. Ferraroni, S. Bürger, L. Steimer, G. Peng, F. Briganti, and A. Stolz. Biochimica et biophysica acta, 1854 (10, A): 1425-1437 (2015)Substrate promiscuity and active site differences in gentisate 1,2-dioxygenases : electron paramagnetic resonance studyA. Aleshintsev, E. Eppinger, J. Gröning, A. Stolz, and R. Gupta. Journal of Biological Inorganic Chemistry, 24 (2): 287-296 (2019)