Substrate-Independent High-Throughput Assay for the Quantification of Aldehydes

被引:31
作者
Ressmann, Anna K. [1 ]
Schwendenwein, Daniel [2 ]
Leonhartsberger, Simon [1 ]
Mihovilovic, Marko D. [1 ]
Bornscheuer, Uwe T. [3 ]
Winkler, Margit [2 ]
Rudroff, Florian [1 ]
机构
[1] TU Wien, Inst Appl Synthet Chem, Getreidemarkt 9-OC 163, A-1060 Vienna, Austria
[2] Acib GmbH, Petersgasse 14, A-8010 Graz, Austria
[3] Greifswald Univ, Dept Biotechnol & Enzyme Catalysis, Inst Biochem, Felix Hausdorff Str 4, D-17487 Greifswald, Germany
基金
奥地利科学基金会;
关键词
aldehyde quantification; 2-amino-benzamidoxime; dihydroquinazoline; high-throughput screening; cell compatible assay; THREONINE ALDOLASES; DIRECTED EVOLUTION; PROTEIN-PRODUCTION; IDENTIFICATION; AUTOINDUCTION; EXPRESSION; REDUCTASE; ENZYMES;
D O I
10.1002/adsc.201900154
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The selective and direct reduction of carboxylic acids into the corresponding aldehydes by chemical methods is still a challenging task in synthesis. Several reductive and oxidative chemical methods are known to produce aldehydes, but most of them require expensive reagents, special reaction conditions, are two-step procedures and often lack chemoselectivity. Nature provides an elegant tool, so called carboxylic acid reductases (CARs) for the direct reduction of carboxylic acids to aldehydes. Discovery as well as engineering of novel CAR enzymes necessitates a robust, product selective high-throughput assay (HTA). We report a simple and fast HTA that allows the substrate-independent and chemoselective quantification of aldehydes (irrespective of their chemical structure) and is sensitive to the nM range. The HTA was validated by NMR and GC analyses and in microbial cells by reexamination of the substrate scope of CAR from Nocardia iowensis (CAR(Ni)). The results were fully consistent with reported data.
引用
收藏
页码:2538 / 2543
页数:6
相关论文
共 36 条
[1]   Engineering the third wave of biocatalysis [J].
Bornscheuer, U. T. ;
Huisman, G. W. ;
Kazlauskas, R. J. ;
Lutz, S. ;
Moore, J. C. ;
Robins, K. .
NATURE, 2012, 485 (7397) :185-194
[2]   Microbial production of scent and flavor compounds [J].
Carroll, Austin L. ;
Desai, Shuchi H. ;
Atsumi, Shota .
CURRENT OPINION IN BIOTECHNOLOGY, 2016, 37 :8-15
[3]   Asymmetric Organocatalysis Combined with Metal Catalysis: Concept, Proof of Concept, and Beyond [J].
Chen, Dian-Feng ;
Han, Zhi-Yong ;
Zhou, Xiao-Le ;
Gong, Liu-Zhu .
ACCOUNTS OF CHEMICAL RESEARCH, 2014, 47 (08) :2365-2377
[4]  
Corey E.J., 1991, ANGEW CHEMIE, V103, P469
[5]   THE LOGIC OF CHEMICAL SYNTHESIS - MULTISTEP SYNTHESIS OF COMPLEX CARBOGENIC MOLECULES [J].
COREY, EJ .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1991, 30 (05) :455-465
[6]   A Retrosynthesis Approach for Biocatalysis in Organic Synthesis [J].
de Souza, Rodrigo O. M. A. ;
Miranda, Leandro S. M. ;
Bornscheuer, Uwe T. .
CHEMISTRY-A EUROPEAN JOURNAL, 2017, 23 (50) :12040-12063
[7]   13C-labeled aldopentoses:: detection and quantitation of cyclic and acyclic forms by heteronuclear 1D and 2D NMR spectroscopy [J].
Drew, KN ;
Zajicek, J ;
Bondo, G ;
Bose, B ;
Serianni, AS .
CARBOHYDRATE RESEARCH, 1998, 307 (3-4) :199-209
[8]  
Fernandez-Alvaro E., 2011, ANGEW CHEM, V123, P8742
[9]   A Combination of In Vivo Selection and Cell Sorting for the Identification of Enantioselective Biocatalysts [J].
Fernandez-Alvaro, Elena ;
Snajdrova, Radka ;
Jochens, Helge ;
Davids, Timo ;
Boettcher, Dominique ;
Bornscheuer, Uwe T. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2011, 50 (37) :8584-8587
[10]   Threonine aldolases: perspectives in engineering and screening the enzymes with enhanced substrate and stereo specificities [J].
Fesko, Kateryna .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2016, 100 (06) :2579-2590