scholarly journals Highly Efficient Access to ( S )‐Sulfoxides Utilizing a Promiscuous Flavoprotein Monooxygenase in a Whole‐Cell Biocatalyst Format

ChemCatChem ◽  
2020 ◽  
Vol 12 (18) ◽  
pp. 4664-4671 ◽  
Author(s):  
Christian Willrodt ◽  
Janosch A. D. Gröning ◽  
Philipp Nerke ◽  
Rainhard Koch ◽  
Anika Scholtissek ◽  
...  
Keyword(s):  
Whole Cell ◽  
Highly Efficient ◽  
Efficient Access ◽  
Whole Cell Biocatalyst

scholarly journals Highly Efficient Synthesis of Optically Pure (S )-1-phenyl-1,2-ethanediol by a Self-Sufficient Whole Cell Biocatalyst

ChemistryOpen ◽  
2015 ◽  
Vol 4 (4) ◽  
pp. 483-488 ◽  
Author(s):  
Xi Chen ◽  
Ting Mei ◽  
Yunfeng Cui ◽  
Qijia Chen ◽  
Xiangtao Liu ◽  
...  
Keyword(s):  
Efficient Synthesis ◽  
Whole Cell ◽  
Highly Efficient ◽  
Whole Cell Biocatalyst ◽  
Optically Pure

Visible light-driven, external mediator-free H2 production by a combination of a photosensitizer and a whole-cell biocatalyst: Escherichia coli expressing [FeFe]-hydrogenase and maturase genes

2020 ◽  
Vol 10 (17) ◽  
pp. 6006-6012 ◽  
Author(s):  
Yuki Honda ◽  
Yuka Shinohara ◽  
Hiroshi Fujii
Keyword(s):  
Escherichia Coli ◽  
Visible Light ◽  
Production System ◽  
H2 Production ◽  
Genetically Engineered ◽  
Whole Cell ◽  
Highly Efficient ◽  
Whole Cell Biocatalyst ◽  
Visible Light Driven

A new visible light-driven, external mediator-free, and highly efficient H2 production system is developed based on the combination of a photosensitizer and a living whole-cell biocatalyst: genetically engineered Escherichia coli.

Highly efficient biodiesel production by a whole-cell biocatalyst employing a system with high lipase expression in Aspergillus oryzae

2011 ◽  
Vol 90 (3) ◽  
pp. 1171-1177 ◽  
Author(s):  
Tomohiro Takaya ◽  
Risa Koda ◽  
Daisuke Adachi ◽  
Kazunori Nakashima ◽  
Junpei Wada ◽  
...  
Keyword(s):  
Aspergillus Oryzae ◽  
Biodiesel Production ◽  
Whole Cell ◽  
Highly Efficient ◽  
Whole Cell Biocatalyst ◽  
Lipase Expression

scholarly journals Tuning a bi-enzymatic cascade reaction in Escherichia coli to facilitate NADPH regeneration for ε-caprolactone production

2021 ◽  
Vol 8 (1) ◽  
Author(s):  
Jinghui Xiong ◽  
Hefeng Chen ◽  
Ran Liu ◽  
Hao Yu ◽  
Min Zhuo ◽  
...  
Keyword(s):  
Escherichia Coli ◽  
Binding Sites ◽  
Regeneration System ◽  
Nadph Regeneration ◽  
Whole Cell ◽  
Cyclohexanone Monooxygenase ◽  
Ribosome Binding ◽  
Ribosome Binding Sites ◽  
Whole Cell Biocatalyst ◽  
Substrate Tolerance

Abstractε-Caprolactone is a monomer of poly(ε-caprolactone) which has been widely used in tissue engineering due to its biodegradability and biocompatibility. To meet the massive demand for this monomer, an efficient whole-cell biocatalytic approach was constructed to boost the ε-caprolactone production using cyclohexanol as substrate. Combining an alcohol dehydrogenase (ADH) with a cyclohexanone monooxygenase (CHMO) in Escherichia coli, a self-sufficient NADPH-cofactor regeneration system was obtained. Furthermore, some improved variants with the better substrate tolerance and higher catalytic ability to ε-caprolactone production were designed by regulating the ribosome binding sites. The best mutant strain exhibited an ε-caprolactone yield of 0.80 mol/mol using 60 mM cyclohexanol as substrate, while the starting strain only got a conversion of 0.38 mol/mol when 20 mM cyclohexanol was supplemented. The engineered whole-cell biocatalyst was used in four sequential batches to achieve a production of 126 mM ε-caprolactone with a high molar yield of 0.78 mol/mol.

Antityrosinase Mechanism and Antimelanogenic Effect of Arbutin Esters Synthesis Catalyzed by Whole-Cell Biocatalyst

2021 ◽  
Vol 69 (14) ◽  
pp. 4243-4252
Author(s):  
Haixia Xu ◽  
Xiaofeng Li ◽  
Xuan Xin ◽  
Lan Mo ◽  
Yucong Zou ◽  
...  
Keyword(s):  
Whole Cell ◽  
Whole Cell Biocatalyst

Enantioselective synthesis of tetrahydroisoquinolines via catalytic intramolecular asymmetric reductive amination

2021 ◽  
Author(s):  
Ruixia Liu ◽  
Jingkuo Han ◽  
Bin Li ◽  
Xian Liu ◽  
Zhao Wei ◽  
...  
Keyword(s):  
Reductive Amination ◽  
Enantioselective Synthesis ◽  
Iridium Complex ◽  
Highly Efficient ◽  
Efficient Access

A highly efficient intramolecular asymmetric reductive amination transformation catalyzed by an iridium complex of tBu-ax-Josiphos has been realized, providing an efficient access to various THIQ alkaloids.

Engineered whole-cell biocatalyst-based detoxification and detection of neurotoxic organophosphate compounds

2014 ◽  
Vol 32 (3) ◽  
pp. 652-662 ◽  
Author(s):  
Chang Sup Kim ◽  
Jeong Hyun Seo ◽  
Dong Gyun Kang ◽  
Hyung Joon Cha
Keyword(s):  
Whole Cell ◽  
Organophosphate Compounds ◽  
Whole Cell Biocatalyst
Sign in / Sign up

Export Citation Format

Share Document