Fabio Parmeggiani
Fabio Parmeggiani
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Exploring the repeat protein universe through computational protein design
TJ Brunette, F Parmeggiani, PS Huang, G Bhabha, DC Ekiert, ...
Nature 528 (7583), 580-584, 2015
Synthesis of D‐ and L‐Phenylalanine Derivatives by Phenylalanine Ammonia Lyases: A Multienzymatic Cascade Process
F Parmeggiani, SL Lovelock, NJ Weise, ST Ahmed, NJ Turner
Angewandte Chemie 127 (15), 4691-4694, 2015
Synthetic and therapeutic applications of ammonia-lyases and aminomutases
F Parmeggiani, NJ Weise, ST Ahmed, NJ Turner
Chemical reviews 118 (1), 73-118, 2018
Thermodynamic benchmark study using Biacore technology
I Navratilova, GA Papalia, RL Rich, D Bedinger, S Brophy, B Condon, ...
Analytical Biochemistry 364 (1), 67-77, 2007
Computational design of self-assembling cyclic protein homo-oligomers
JA Fallas, G Ueda, W Sheffler, V Nguyen, DE McNamara, B Sankaran, ...
Nature chemistry 9 (4), 353-360, 2017
Biosynthesis and Characterization of Copper Nanoparticles Using Shewanella oneidensis: Application for Click Chemistry
RL Kimber, EA Lewis, F Parmeggiani, K Smith, H Bagshaw, T Starborg, ...
Small 14 (10), 1703145, 2018
Biotechnological Development of a Practical Synthesis of Ethyl (S)-2-Ethoxy-3-(p-methoxyphenyl)propanoate (EEHP): Over 100-Fold Productivity Increase from …
M Bechtold, E Brenna, C Femmer, FG Gatti, S Panke, F Parmeggiani, ...
Organic Process Research & Development 16 (2), 269-276, 2012
Enoate Reductase-Mediated Preparation of Methyl (S)-2-Bromobutanoate, a Useful Key Intermediate for the Synthesis of Chiral Active Pharmaceutical Ingredients
E Brenna, FG Gatti, A Manfredi, D Monti, F Parmeggiani
Organic Process Research & Development 16 (2), 262-268, 2012
The bacterial ammonia lyase EncP: a tunable biocatalyst for the synthesis of unnatural amino acids
NJ Weise, F Parmeggiani, ST Ahmed, NJ Turner
Journal of the American Chemical Society 137 (40), 12977-12983, 2015
Biocatalytic transamination with near-stoichiometric inexpensive amine donors mediated by bifunctional mono-and di-amine transaminases
JL Galman, I Slabu, NJ Weise, C Iglesias, F Parmeggiani, RC Lloyd, ...
Green Chemistry 19 (2), 361-366, 2017
Cascade coupling of ene reductases with alcohol dehydrogenases: Enantioselective reduction of prochiral unsaturated aldehydes
E Brenna, FG Gatti, D Monti, F Parmeggiani, A Sacchetti
ChemCatChem 4 (5), 653-659, 2012
Adenylation activity of carboxylic acid reductases enables the synthesis of amides
AJL Wood, NJ Weise, JD Frampton, MS Dunstan, MA Hollas, ...
Angewandte Chemie 129 (46), 14690-14693, 2017
Chemoenzymatic Synthesis of Optically Pure l- and d-Biarylalanines through Biocatalytic Asymmetric Amination and Palladium-Catalyzed Arylation
ST Ahmed, F Parmeggiani, NJ Weise, SL Flitsch, NJ Turner
ACS Catalysis 5 (9), 5410-5413, 2015
Real-time screening of biocatalysts in live bacterial colonies
C Yan, F Parmeggiani, EA Jones, E Claude, SA Hussain, NJ Turner, ...
Journal of the American Chemical Society 139 (4), 1408-1411, 2017
Synthesis of robalzotan, ebalzotan, and rotigotine precursors via the stereoselective multienzymatic cascade reduction of α, β-unsaturated aldehydes
E Brenna, FG Gatti, L Malpezzi, D Monti, F Parmeggiani, A Sacchetti
The Journal of Organic Chemistry 78 (10), 4811-4822, 2013
Opposite Enantioselectivity in the Bioreduction of (Z)‐β‐Aryl‐β‐cyanoacrylates Mediated by the Tryptophan 116 Mutants of Old Yellow Enzyme 1: Synthetic Approach to (R)‐and (S …
E Brenna, M Crotti, FG Gatti, D Monti, F Parmeggiani, RW Powell III, ...
Advanced Synthesis & Catalysis 357 (8), 1849-1860, 2015
Single‐Biocatalyst Synthesis of Enantiopure d‐Arylalanines Exploiting an Engineered d‐Amino Acid Dehydrogenase
F Parmeggiani, ST Ahmed, MP Thompson, NJ Weise, JL Galman, ...
Advanced Synthesis & Catalysis 358 (20), 3298-3306, 2016
Old Yellow Enzyme-mediated reduction of β-cyano-α, β-unsaturated esters for the synthesis of chiral building blocks: stereochemical analysis of the reaction
E Brenna, FG Gatti, A Manfredi, D Monti, F Parmeggiani
Catalysis Science & Technology 3 (4), 1136-1146, 2013
Preparation and luminescence thermochromism of tetranuclear copper (I)–pyridine–iodide clusters
F Parmeggiani, A Sacchetti
Journal of Chemical Education 89 (7), 946-949, 2012
Productivity enhancement of C= C bioreductions by coupling the in situ substrate feeding product removal technology with isolated enzymes.
E Brenna, FG Gatti, D Monti, F Parmeggiani, A Sacchetti
Chemical Communications (Cambridge, England) 48 (1), 79-81, 2011
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