Conversion of phenylglycinonitrile by recombinant Escherichia coli cells synthesizing variants of the arylacetonitrilase from Pseudomonas fluorescens EBC191-Reference-Cited by-同舟云学术

Conversion of phenylglycinonitrile by recombinant Escherichia coli cells synthesizing variants of the arylacetonitrilase from Pseudomonas fluorescens EBC191

Published:2019-06-20 Issue:16 Volume:103 Page:6737-6746
ISSN:0175-7598
Container-title:Applied Microbiology and Biotechnology
language:en
Short-container-title:Appl Microbiol Biotechnol

Author:

Eppinger Erik,Stolz Andreas^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Applied Microbiology and Biotechnology,General Medicine,Biotechnology

Link

http://link.springer.com/content/pdf/10.1007/s00253-019-09957-y.pdf

Reference45 articles.

1. Baum S, Williamson DS, Sewell T, Stolz A (2012) Conversion of sterically demanding α,α-disubstituted phenylacetonitriles by the arylacetonitrilase from Pseudomonas fluorescens EBC191. Appl Environ Microbiol 78:48–57

2. Bhalla TC, Miura A, Wakamoto A, Ohba Y, Furuhashi K (1992) Asymmetric hydrolysis of α-aminonitriles to optically active amino acids by a nitrilase of Rhodococcus rhodochrous PA-34. Appl Microbiol Biotechnol 37:184–190

3. Bhalla TC, Kumar V, Kumar V, Thakur N, Savitri (2018) Nitrile metabolizing enzymes in biocatalysis and biotransformation. Appl Biochem Biotechnol 185:925–946

4. Bhosale M, Pande S, Kumar A, Kairamkonda S, Nandi D (2010) Characterization of two M17 family members in Escherichia coli, peptidase A and peptidase B. Biochem Biophys Res Comm 395:76–81

5. Bruggink A (2001) Synthesis of β-lactam antibiotics: chemistry, biocatalysis & process integration. Kluwer Academic Publishers, Dordrecht

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Bidirectional Regulation of Nitrilase Reaction Specificity by Tuning the Characteristic Distances between Key Residues and Substrate;ACS Catalysis;2023-07-23

2. Rational identification of a catalytically promiscuous nitrilase by predicting a unique catalytic triad motif feature through an in silico strategy;Catalysis Science & Technology;2023

3. Chemoenzymatic enantioselective synthesis of phenylglycine and phenylglycine amide by direct coupling of the Strecker synthesis with a nitrilase reaction;Frontiers in Catalysis;2022-08-05

4. Emerging Technique of Enzymatic Biotransformation of Amides to Hydroxamic Acid for Pharmaceutical and Dye Waste Treatment;Innovations in Environmental Biotechnology;2022

5. Proposed mechanism for post‐translational self‐modification of Co‐NHase based on Co 2+ diffusion limitation;Biotechnology Journal;2021-08-21