The Reductive Amination of Carbonyl Compounds Using Native Amine Dehydrogenase from Laribacter hongkongensis

2021 ◽  
Vol 26 (3) ◽  
pp. 384-391
Author(s):  
Somin Lee ◽  
Hyunwoo Jeon ◽  
Pritam Giri ◽  
Uk-Jae Lee ◽  
Hyunsang Jung ◽  
...  
2010 ◽  
Vol 40 (7) ◽  
pp. 951-956 ◽  
Author(s):  
Heshmatollah Alinezhad ◽  
Mahmood Tajbakhsh ◽  
Nastaran Mahdavi

ACS Catalysis ◽  
2020 ◽  
Vol 10 (14) ◽  
pp. 7763-7772 ◽  
Author(s):  
Chao Xie ◽  
Jinliang Song ◽  
Manli Hua ◽  
Yue Hu ◽  
Xin Huang ◽  
...  

Catalysts ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1451
Author(s):  
Heyu Huo ◽  
Guangxiao Yao ◽  
Shizhen Wang

Chiral amines are key building blocks for pharmaceuticals. Economic assessment of commercial potential of bioprocesses is needed for guiding research. Biosynthesis of (S)-α-methylbenzylamine (MBA) was selected as case study. For transamination route, transaminase coupled with glucose dehydrogenase and lactate dehydrogenase catalyzed the reaction with NADH (Nicotinamide adenine dinucleotide) regeneration. Amine dehydrogenase coupled with NADH oxidase, which catalyzed the reductive amination process. Comparison of biosynthesis cost by reductive amination and transamination routes was carried out. Economic assessment based on the framework of cost analysis and preliminary process information revealed that cost is greatly dependent on enzyme price. The results indicated that enhancing the activity of amine dehydrogenase by 4–5 folds can drop the unit price of reductive amination to $0.5–0.6/g, which make it competitive with transamination route.


2020 ◽  
Vol 8 (46) ◽  
pp. 17054-17061
Author(s):  
Rui-Feng Cai ◽  
Lei Liu ◽  
Fei-Fei Chen ◽  
Aitao Li ◽  
Jian-He Xu ◽  
...  

Tetrahedron ◽  
2005 ◽  
Vol 61 (8) ◽  
pp. 2105-2109 ◽  
Author(s):  
Tomoaki Ikenaga ◽  
Kumiko Matsushita ◽  
Junichi Shinozawa ◽  
Satoru Yada ◽  
Yuzuru Takagi

2020 ◽  
Vol 56 (61) ◽  
pp. 8691-8694
Author(s):  
Mohanad A. Hussein ◽  
An H. Dinh ◽  
Vien T. Huynh ◽  
Thanh Vinh Nguyen

Triflic acid efficiently promotes the reductive amination reactions of carbonyl compounds on a broad range of substrates.


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