Artificial Biocatalytic Linear Cascades to Access Hydroxy Acids, Lactones, and α- and β-Amino Acids
暂无分享,去创建一个
[1] Frank Baganz,et al. Conscious coupling: The challenges and opportunities of cascading enzymatic microreactors. , 2017, Biotechnology journal.
[2] U. Bornscheuer,et al. An alternative approach towards poly-ε-caprolactone through a chemoenzymatic synthesis: combined hydrogenation, bio-oxidations and polymerization without the isolation of intermediates , 2017 .
[3] P. Perlmutter,et al. β-amino acids: Versatile peptidomimetics , 2002 .
[4] Yuguo Zheng,et al. Enantioselective cascade biocatalysis for deracemization of 2-hydroxy acids using a three-enzyme system , 2016, Microbial Cell Factories.
[5] Christian Wandrey,et al. Industrial Biocatalysis: Past, Present, and Future , 2000 .
[6] Marco W Fraaije,et al. Coupled reactions by coupled enzymes: alcohol to lactone cascade with alcohol dehydrogenase–cyclohexanone monooxygenase fusions , 2017, Applied Microbiology and Biotechnology.
[7] Hyungdon Yun,et al. Asymmetric synthesis of aromatic β‐amino acids using ω‐transaminase: Optimizing the lipase concentration to obtain thermodynamically unstable β‐keto acids , 2016, Biotechnology journal.
[8] U. Bornscheuer,et al. An Enzymatic Toolbox for Cascade Reactions: A Showcase for an In Vivo Redox Sequence in Asymmetric Synthesis , 2013 .
[9] H. Hoffmann,et al. Synthese und biologische Aktivitt von a-Methylen-?-butyrolactonen , 1985 .
[10] U. Bornscheuer,et al. A self-sufficient Baeyer-Villiger biocatalysis system for the synthesis of ɛ-caprolactone from cyclohexanol. , 2013, Enzyme and microbial technology.
[11] Shuke Wu,et al. Cascade Biocatalysis for Sustainable Asymmetric Synthesis: From Biobased l-Phenylalanine to High-Value Chiral Chemicals. , 2016, Angewandte Chemie.
[12] A. Porto,et al. Biocatalysis and biotransformation in Brazil: An overview. , 2015, Biotechnology advances.
[13] Wolfgang Kroutil,et al. Deracemisation of Mandelic Acid to Optically Pure Non-Natural L-Phenylglycine via a Redox-Neutral Biocatalytic Cascade , 2010 .
[14] D. Opperman,et al. One‐pot Conversion of Cycloalkanes to Lactones , 2015 .
[15] W. Thielemans,et al. Synthesis of polycaprolactone: a review. , 2009, Chemical Society reviews.
[16] C. Syldatk,et al. Hydantoinases and related enzymes as biocatalysts for the synthesis of unnatural chiral amino acids. , 2001, Current opinion in biotechnology.
[17] Joerg H. Schrittwieser,et al. Artificial Biocatalytic Linear Cascades for Preparation of Organic Molecules. , 2018, Chemical reviews.
[18] C. Benezra,et al. Stereospecificity in allergic contact dermatitis to simple substituted methylene lactone derivatives. , 1987, Journal of medicinal chemistry.
[19] Renata Sigrist,et al. Nature-inspired enzymatic cascades to build valuable compounds. , 2015, Biotechnology advances.
[20] A. C. Marr,et al. Combining bio- and chemo-catalysis: from enzymes to cells, from petroleum to biomass. , 2011, Trends in biotechnology.
[21] S. Servi,et al. Chemo-enzymatic deracemization methods for the preparation of enantiopure non-natural α-amino acids , 2008 .
[22] Wolfgang Kroutil,et al. Recent biocatalytic oxidation–reduction cascades , 2011, Current opinion in chemical biology.
[23] C. Denard,et al. Multistep One-Pot Reactions Combining Biocatalysts and Chemical Catalysts for Asymmetric Synthesis , 2013 .
[24] C. Hertweck,et al. The biosynthetic logic of polyketide diversity. , 2009, Angewandte Chemie.
[25] D. Seebach,et al. The World of β‐ and γ‐Peptides Comprised of Homologated Proteinogenic Amino Acids and Other Components , 2004 .
[26] U. Bornscheuer,et al. Cascade catalysis--strategies and challenges en route to preparative synthetic biology. , 2015, Chemical communications.
[27] Heng-Phon Too,et al. Highly regio- and enantioselective multiple oxy- and amino-functionalizations of alkenes by modular cascade biocatalysis , 2016, Nature Communications.
[28] A. Mosandl,et al. Stereoisomeric flavor compounds. 20. Structure and properties of .gamma.-lactone enantiomers , 1989 .
[29] M. Hahn,et al. Alicyclic β-amino acids in Medicinal Chemistry , 2005, Amino Acids.
[30] Wolfgang Kroutil,et al. Recent Developments of Cascade Reactions Involving ω‑Transaminases , 2014 .
[31] Zhi Li,et al. Cascade Biotransformations via Enantioselective Reduction, Oxidation, and Hydrolysis: Preparation of (R)-δ-Lactones from 2-Alkylidenecyclopentanones , 2013 .
[32] Wolfgang Kroutil,et al. Biocatalytic One-Pot Synthesis of l-Tyrosine Derivatives from Monosubstituted Benzenes, Pyruvate, and Ammonia , 2015 .
[33] Shuke Wu,et al. Organic Synthesis via Oxidative Cascade Biocatalysis , 2016, Synlett.
[34] Joerg H. Schrittwieser,et al. Multi-Enzymatic Cascade Reactions: Overview and Perspectives , 2011 .
[35] Florian Rudroff,et al. Opportunities and challenges for combining chemo- and biocatalysis , 2018, Nature Catalysis.
[36] M. Reetz,et al. Towards Practical Baeyer–Villiger‐Monooxygenases: Design of Cyclohexanone Monooxygenase Mutants with Enhanced Oxidative Stability , 2010, Chembiochem : a European journal of chemical biology.
[37] T. Roberts,et al. Synthetic Biology for Cell-Free Biosynthesis: Fundamentals of Designing Novel In Vitro Multi-Enzyme Reaction Networks. , 2018, Advances in biochemical engineering/biotechnology.
[38] J. D. Del Valle,et al. Chemistry and biology of the aeruginosin family of serine protease inhibitors. , 2008, Angewandte Chemie.
[39] E. Jacobsen,et al. Scaleable catalytic asymmetric Strecker syntheses of unnatural α-amino acids , 2009, Nature.
[40] J. Pietruszka,et al. Stereoselective Enzyme Cascades: An Efficient Synthesis of Chiral γ-Butyrolactones , 2014 .
[41] Peiyuan Yao,et al. Efficient Biosynthesis of Ethyl (R)‐3‐Hydroxyglutarate through a One‐Pot Bienzymatic Cascade of Halohydrin Dehalogenase and Nitrilase , 2015 .
[42] O. Kurita,et al. Structure of a new antifungal C11-hydroxyfatty acid isolated from leaves of wild rice (Oryza officinalis) , 1995 .
[43] M. Kaiser,et al. Challenges in the Syntheses of Peptidic Natural Products , 2012 .
[44] I. Lavandera,et al. Why Leave a Job Half Done? Recent Progress in Enzymatic Deracemizations , 2015 .
[45] U. Bornscheuer,et al. Identification, Characterization, and Application of Three Enoate Reductases from Pseudomonas putida in In Vitro Enzyme Cascade Reactions , 2014 .
[46] Isabel Oroz‐Guinea,et al. Enzyme catalysed tandem reactions. , 2013, Current Opinion in Chemical Biology.
[47] U. Bornscheuer,et al. Kinetic insights into ϵ‐caprolactone synthesis: Improvement of an enzymatic cascade reaction , 2017, Biotechnology and bioengineering.
[48] Lorna J. Hepworth,et al. Constructing Biocatalytic Cascades: In Vitro and in Vivo Approaches to de Novo Multi-Enzyme Pathways , 2017 .
[49] Constance B. Bailey,et al. Preparative, in Vitro Biocatalysis of Triketide Lactone Chiral Building Blocks , 2012, Chembiochem : a European journal of chemical biology.
[50] E. Busto,et al. Biocontrolled formal inversion or retention of L-α-amino acids to enantiopure (R)- or (S)-hydroxyacids. , 2014, Chemistry.
[51] Jin‐Byung Park,et al. Production of ω-hydroxyundec-9-enoic acid and n-heptanoic acid from ricinoleic acid by recombinant Escherichia coli-based biocatalyst , 2014 .
[52] U. Bornscheuer,et al. An enzyme cascade synthesis of ε-caprolactone and its oligomers. , 2015, Angewandte Chemie.
[53] F. Parmeggiani,et al. Single-Biocatalyst Synthesis of Enantiopure D-Arylalanines Exploiting an Engineered D-Amino Acid Dehydrogenase , 2016 .
[54] Nicholas J Turner,et al. Enantioselective oxidation of C-O and C-N bonds using oxidases. , 2011, Chemical reviews.
[55] Uwe T. Bornscheuer,et al. Direct biocatalytic one-pot-transformation of cyclohexanol with molecular oxygen into ɛ-caprolactone. , 2013, Enzyme and microbial technology.
[56] P. Schultz,et al. Expanding the genetic code. , 2002, Chemical communications.
[57] Uwe T. Bornscheuer,et al. Biocatalytic Access to Chiral Polyesters by an Artificial Enzyme Cascade Synthesis , 2015 .
[58] E. Balskus,et al. Opportunities for merging chemical and biological synthesis. , 2014, Current opinion in biotechnology.
[59] Wolfgang Kroutil,et al. Introduction to ACS Catalysis Virtual Special Issue on Cascade Catalysis , 2014 .
[60] J. Bäckvall,et al. Combination of enzymes and metal catalysts. A powerful approach in asymmetric catalysis. , 2003, Chemical reviews.
[61] Krist V. Gernaey,et al. Multienzyme-Catalyzed Processes: Next-Generation Biocatalysis , 2011 .
[62] R. Agrawal. The first approved agent in the Glitazar's Class: Saroglitazar. , 2014, Current drug targets.
[63] Florian Rudroff,et al. Fusion proteins of an enoate reductase and a Baeyer-Villiger monooxygenase facilitate the synthesis of chiral lactones , 2017, Biological chemistry.
[64] Florian Rudroff,et al. In vitro characterization of an enzymatic redox cascade composed of an alcohol dehydrogenase, an enoate reductases and a Baeyer–Villiger monooxygenase , 2014, Journal of biotechnology.
[65] Jian‐He Xu,et al. A novel D-mandelate dehydrogenase used in three-enzyme cascade reaction for highly efficient synthesis of non-natural chiral amino acids. , 2015, Journal of biotechnology.
[66] J. A. Vale,et al. Rapid conversion of cyclohexenone, cyclohexanone and cyclohexanol to ε-caprolactone by whole cells of Geotrichum candidum CCT 1205 , 2017 .
[67] Dörte Rother,et al. (Chemo)enzymatic cascades - Nature's synthetic strategy transferred to the laboratory , 2015 .
[68] Frank Hollmann,et al. A Bi‐enzymatic Convergent Cascade for ε‐Caprolactone Synthesis Employing 1,6‐Hexanediol as a ‘Double‐Smart Cosubstrate’ , 2015 .
[69] Andreas Martin,et al. Synthesis of azelaic acid from vegetable oil-based feedstocks , 2011 .
[70] Jinwon Lee,et al. Adding value to plant oils and fatty acids: Biological transformation of fatty acids into ω-hydroxycarboxylic, α,ω-dicarboxylic, and ω-aminocarboxylic acids. , 2015, Journal of biotechnology.
[71] Johannes Kabisch,et al. Co-expression of an alcohol dehydrogenase and a cyclohexanone monooxygenase for cascade reactions facilitates the regeneration of the NADPH cofactor. , 2018, Enzyme and microbial technology.
[72] Bernhard Hauer,et al. Enzyme engineering in the context of novel pathways and products. , 2015, Current opinion in biotechnology.
[73] M. Fischbach,et al. Assembly-line enzymology for polyketide and nonribosomal Peptide antibiotics: logic, machinery, and mechanisms. , 2006, Chemical reviews.
[74] Nicholas J Turner,et al. Artificial concurrent catalytic processes involving enzymes. , 2015, Chemical communications.
[75] Wolfgang Kroutil,et al. One-Pot, Two-Module Three-Step Cascade To Transform Phenol Derivatives to Enantiomerically Pure (R)- or (S)-p-Hydroxyphenyl Lactic Acids , 2016 .
[76] F. Fülöp,et al. Application of alicyclic β-amino acids in peptide chemistry , 2006 .
[77] H. Gröger,et al. Combining the 'two worlds' of chemocatalysis and biocatalysis towards multi-step one-pot processes in aqueous media. , 2014, Current opinion in chemical biology.
[78] Christian C. Gruber,et al. From a Racemate to a Single Enantiomer: Deracemization by Stereoinversion , 2006 .
[79] B. Martín‐Matute,et al. Dynamic kinetic resolution catalyzed by enzymes and metals. , 2007, Current opinion in chemical biology.
[80] U. Bornscheuer,et al. Multistep enzymatic synthesis of long-chain α,ω-dicarboxylic and ω-hydroxycarboxylic acids from renewable fatty acids and plant oils. , 2013, Angewandte Chemie.
[81] N. Turner,et al. Enzymatic cascades for the regio- and stereoselective synthesis of chiral amines , 2015 .
[82] R. Marchelli,et al. The potential of enantioselective analysis as a quality control tool , 1996 .
[83] Fang Zhang,et al. Production of Sebacic Acid Using Two-Phase Bipolar Membrane Electrodialysis , 2009 .