Inverting the enantioselectivity of P450pyr monooxygenase by directed evolution.
暂无分享,去创建一个
Huimin Zhao | Zhi Li | Weng Lin Tang | Huimin Zhao | Zhi Li
[1] W. Marsden. I and J , 2012 .
[2] Manfred T Reetz,et al. Shedding light on the efficacy of laboratory evolution based on iterative saturation mutagenesis. , 2009, Molecular bioSystems.
[3] Dongmei Cui,et al. Supplementary Material (ESI) for Chemical Communications , 2009 .
[4] Hideo Nakano,et al. Inverting enantioselectivity of Burkholderia cepacia KWI-56 lipase by combinatorial mutation and high-throughput screening using single-molecule PCR and in vitro expression. , 2003, Journal of molecular biology.
[5] Frances H Arnold,et al. Evolutionary history of a specialized p450 propane monooxygenase. , 2008, Journal of molecular biology.
[6] E. G. Funhoff,et al. Cytochrome P450 Alkane Hydroxylases of the CYP153 Family Are Common in Alkane-Degrading Eubacteria Lacking Integral Membrane Alkane Hydroxylases , 2006, Applied and Environmental Microbiology.
[7] Frances H Arnold,et al. Regio- and enantioselective alkane hydroxylation with engineered cytochromes P450 BM-3. , 2003, Journal of the American Chemical Society.
[8] J. Bercaw,et al. Understanding and exploiting C–H bond activation , 2002, Nature.
[9] I. Alfonso,et al. Asymmetric organic synthesis with enzymes , 2008 .
[10] S. Bell,et al. The heme monooxygenase cytochrome P450cam can be engineered to oxidize ethane to ethanol. , 2005, Angewandte Chemie.
[11] V. Urlacher,et al. Altering the Regioselectivity of Cytochrome P450 CYP102A3 of Bacillus subtilis by Using a New Versatile Assay System , 2006, Chembiochem : a European journal of chemical biology.
[12] C. Hu,et al. "Cassette" in situ enzymatic screening identifies complementary chiral scaffolds for hydrolytic kinetic resolution across a range of epoxides. , 2007, Angewandte Chemie.
[13] J. Hasegawa,et al. Characterization of novel alcohol dehydrogenase of Devosia riboflavina involved in stereoselective reduction of 3-pyrrolidinone derivatives , 2008 .
[14] B. Witholt,et al. Preparation of (S)-N-substituted 4-hydroxy-pyrrolidin-2-ones by regio- and stereoselective hydroxylation with Sphingomonas sp. HXN-200. , 2000, Organic letters.
[15] F. Arnold,et al. Laboratory evolution of cytochrome P450 BM‐3 monooxygenase for organic cosolvents , 2004, Biotechnology and bioengineering.
[16] B. Witholt,et al. Regio- and stereoselective hydroxylation of N-substituted piperidin-2-ones with Sphingomonas sp. HXN-200 , 2002 .
[17] F. Arnold,et al. Thermostabilization of a Cytochrome P450 Peroxygenase , 2003, Chembiochem : a European journal of chemical biology.
[18] K. Hult,et al. An S-selective lipase was created by rational redesign and the enantioselectivity increased with temperature. , 2005, Angewandte Chemie.
[19] Jin Zhai,et al. The fabrication and switchable superhydrophobicity of TiO2 nanorod films. , 2005, Angewandte Chemie.
[20] F. Young. Biochemistry , 1955, The Indian Medical Gazette.
[21] Huimin Zhao,et al. Relaxing the nicotinamide cofactor specificity of phosphite dehydrogenase by rational design. , 2003, Biochemistry.
[22] Frances H. Arnold,et al. Inverting enantioselectivity by directed evolution of hydantoinase for improved production of l-methionine , 2000, Nature Biotechnology.
[23] Frances H. Arnold,et al. Laboratory evolution of a soluble, self-sufficient, highly active alkane hydroxylase , 2002, Nature Biotechnology.
[24] B. Witholt,et al. Practical syntheses of N-substituted 3-hydroxyazetidines and 4-hydroxypiperidines by hydroxylation with Sphingomonas sp. HXN-200. , 2002, Organic letters.
[25] R. Rosenfeld. Nature , 2009, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.
[26] Hiroyuki Ohno,et al. Structure and direct electrochemistry of cytochrome P450 from the thermoacidophilic crenarchaeon, Sulfolobus tokodaii strain 7. , 2004, Journal of inorganic biochemistry.
[27] M. Ferrer,et al. Inversion of stereospecificity of vanillyl-alcohol oxidase. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[28] B. Witholt,et al. Preparation of optically active N-benzyl-3-hydroxypyrrolidine by enzymatic hydroxylation , 1999 .
[29] Zhixiang Chang. Recent Advances in Regio- and Stereoselective Biohydroxylation of Non- Activated Carbon Atoms , 2004 .
[30] Huimin Zhao,et al. Evolution in Reverse: Engineering a D‐Xylose‐Specific Xylose Reductase , 2008, Chembiochem : a European journal of chemical biology.
[31] Robert Kourist,et al. Complete inversion of enantioselectivity towards acetylated tertiary alcohols by a double mutant of a Bacillus subtilis esterase. , 2008, Angewandte Chemie.
[32] Per Berglund. Asymmetric Organic Synthesis with Enzymes. Edited by Vicente Gotor, Ignacio Alfonso and Eduardo García-Urdiales. , 2008 .
[33] G. G. Stokes. "J." , 1890, The New Yale Book of Quotations.
[34] David J. Schuller,et al. Crystal Structure of a Thermophilic Cytochrome P450 from the Archaeon Sulfolobus solfataricus * , 2000, The Journal of Biological Chemistry.
[35] Huimin Zhao,et al. Directed evolution of specific receptor-ligand pairs for use in the creation of gene switches. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[36] K. Gruber,et al. Inverting enantioselectivity of Burkholderia gladioli esterase EstB by directed and designed evolution. , 2007, Journal of biotechnology.
[37] B. Witholt,et al. High-throughput measurement of the enantiomeric excess of chiral alcohols by using two enzymes. , 2004, Angewandte Chemie.
[38] Preparation of (R)- and (S)-N-protected 3-hydroxypyrrolidines by hydroxylation with Sphingomonas sp. HXN-200, a highly active, regio- and stereoselective, and easy to handle biocatalyst. , 2001, The Journal of organic chemistry.