Zobrazeno 1 - 10
of 86
pro vyhledávání: '"Zhong-Liu Wu"'
Publikováno v:
Journal of Agricultural and Food Chemistry. 71:2935-2942
Publikováno v:
New Journal of Chemistry. 46:6274-6282
Controllable and mild photoenzymatic production of chiral alcohols was realized by coupling a photochemical NAD(P)H regeneration system with (R)- or (S)-selective ketoreductases.
Publikováno v:
ChemSusChem.
Following a synthetic chemistry blueprint for the valorization of lignocellulosic platform chemicals, this study showcases a so far unprecedented approach to implement non-natural enzyme modules in vivo. For the design of a novel functional whole cel
Publikováno v:
ChemSusChem.
A Zr-based dual-ligand MOFs with pre-installed Rh complex was employed for NADH regeneration in situand also used for immobilization of FDH in order to realize a highly efficient CO2 fixation system. Then, based on the detailed investigations into th
Publikováno v:
Process Biochemistry. 101:207-212
Ketoreductase ChKRED12 catalyzes the asymmetric bioreduction of ethyl 3-oxo-3-(2-thienyl) propanoate to produce the key chiral intermediate of duloxetine. To improve the robustness of the enzyme, we used the FireProt web server to predict potential t
Publikováno v:
Catalysis Science & Technology. 11:2195-2201
Styrene monooxygenases (SMOs) are excellent enzymes for the production of (S)-enantiopure epoxides, but so far, only one (R)-selective SMO has been identified with a narrow substrate spectrum. Mining the NCBI non-redundant protein sequences returned
Publikováno v:
SSRN Electronic Journal.
Publikováno v:
SSRN Electronic Journal.
Publikováno v:
SSRN Electronic Journal.
Publikováno v:
Journal of Microbiology and Biotechnology. 29:1769-1776
Ethyl (S)-3-hydroxy-3-(2-thienyl)propanoate((S)-HEES)acts as a key chiral intermediate for the blockbuster antidepressant drug duloxetine, which canbe achieved viathe stereoselective bioreduction ofethyl 3-oxo-3-(2-thienyl) propanoate (KEES) that con