High‐throughput screening for distinguishing nitrilases from nitrile hydratases in Aspergillus and application of a Box‐Behnken design for the optimization of nitrilase

Author(s):  
Edvan do Carmo Santos ◽  
Luiz Henrique Sales Menezes ◽  
Carolline Silva Santos ◽  
Paulo Vinicius Bispo Santana ◽  
Glêydison Amarante Soares ◽  
...  

2015 ◽  
Vol 46 (1) ◽  
pp. 113-116 ◽  
Author(s):  
Leticia Mara Lima Angelini ◽  
Amanda Ribeiro Martins da Silva ◽  
Lucas de Freitas Coli Rocco ◽  
Cintia Duarte de Freitas Milagre


Planta Medica ◽  
2012 ◽  
Vol 78 (11) ◽  
Author(s):  
L Hingorani ◽  
NP Seeram ◽  
B Ebersole


Planta Medica ◽  
2015 ◽  
Vol 81 (16) ◽  
Author(s):  
K Georgousaki ◽  
N DePedro ◽  
AM Chinchilla ◽  
N Aliagiannis ◽  
F Vicente ◽  
...  


Planta Medica ◽  
2016 ◽  
Vol 81 (S 01) ◽  
pp. S1-S381
Author(s):  
LS Espindola ◽  
RG Dusi ◽  
KR Gustafson ◽  
J McMahon ◽  
JA Beutler


2014 ◽  
Author(s):  
Clair Cochrane ◽  
Halil Ruso ◽  
Anthony Hope ◽  
Rosemary G Clarke ◽  
Christopher Barratt ◽  
...  


2009 ◽  
Vol 37 (3) ◽  
pp. 193-257 ◽  
Author(s):  
Sarvesh Upadhyaya ◽  
Ponnambalam R. Selvaganapathy


2020 ◽  
Author(s):  
Jia Shen Chew ◽  
Ken Chi Lik Lee ◽  
THI THANH NHA HO

<p>Lee and coworkers offers a kind of new concept to enzyme immobilization and explores its suitability in the context of miniaturisation and high-throughput screening. Here, polystyrene-immobilized ketoreductases are compared with its non-immobilized counterparts in terms of conversion and stereoselectivity (both determined by chiral HPLC), and the study indicates that the BioBeads perform similarly (sometimes slightly more selective) which may be useful whenever defined micro-scale amounts of biocatalysts were required in high-throughput experiment settings.</p>



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