High-Throughput Screening Method for Directed Evolution and Characterization of Aldol Activity of D-Threonine Aldolase

Author(s):  
Lei Gong ◽  
Guochao Xu ◽  
Xudong Cao ◽  
Ruizhi Han ◽  
Jinjun Dong ◽  
...  
2019 ◽  
Author(s):  
Huifang Xu ◽  
Weinan Liang ◽  
Linlin Ning ◽  
Yuanyuan Jiang ◽  
Wenxia Yang ◽  
...  

P450 fatty acid decarboxylases (FADCs) have recently been attracting considerable attention owing to their one-step direct production of industrially important 1-alkenes from biologically abundant feedstock free fatty acids under mild conditions. However, attempts to improve the catalytic activity of FADCs have met with little success. Protein engineering has been limited to selected residues and small mutant libraries due to lack of an effective high-throughput screening (HTS) method. Here, we devise a catalase-deficient <i>Escherichia coli</i> host strain and report an HTS approach based on colorimetric detection of H<sub>2</sub>O<sub>2</sub>-consumption activity of FADCs. Directed evolution enabled by this method has led to effective identification for the first time of improved FADC variants for medium-chain 1-alkene production from both DNA shuffling and random mutagenesis libraries. Advantageously, this screening method can be extended to other enzymes that stoichiometrically utilize H<sub>2</sub>O<sub>2</sub> as co-substrate.


2016 ◽  
Vol 52 (50) ◽  
pp. 7854-7857 ◽  
Author(s):  
M. L. Kelty ◽  
W. Morris ◽  
A. T. Gallagher ◽  
J. S. Anderson ◽  
K. A. Brown ◽  
...  

We describe and employ a high-throughput screening method to accelerate the synthesis and identification of pure-phase, nanocrystalline metal–organic frameworks (MOFs).


2012 ◽  
Vol 35 (22) ◽  
pp. 3149-3159 ◽  
Author(s):  
Annette Berg ◽  
Stefan A. Oelmeier ◽  
Jörg Kittelmann ◽  
Florian Dismer ◽  
Jürgen Hubbuch

2014 ◽  
Vol 21 (3) ◽  
pp. 414-421 ◽  
Author(s):  
Raluca Ostafe ◽  
Radivoje Prodanovic ◽  
Jovana Nazor ◽  
Rainer Fischer

2019 ◽  
Vol 133 (1) ◽  
pp. 123-131 ◽  
Author(s):  
Mingai Li ◽  
Luca Cappellin ◽  
Jia Xu ◽  
Franco Biasioli ◽  
Claudio Varotto

Abstract Functional characterization of plant volatile organic compound (VOC) biosynthetic genes and elucidation of the biological function of their products often involve the screening of large numbers of plants from either independent transformation events or mapping populations. The low time resolution of standard gas chromatographic methods, however, represents a major bottleneck for in planta genetic characterization of VOC biosynthetic genes. Here we present a fast and highly-sensitive method for the high-throughput characterization of VOC emission levels/patterns by coupling a Proton Transfer Reaction Time-of-Flight Mass Spectrometer to an autosampler for automation of sample measurement. With this system more than 700 samples per day can be screened, detecting for each sample hundreds of spectrometric peaks in the m/z 15–300 range. As a case study, we report the characterization of VOC emissions from 116 independent Arabidopsis thaliana lines transformed with a putative isoprene synthase gene, confirming its function also when fused to a C-terminal 3×FLAG tag. We demonstrate that the method is more reliable than conventional characterization of transgene expression for the identification of the most highly isoprene-emitting lines. The throughput of this VOC screening method exceeds that of existing alternatives, potentially allowing its application to reverse and forward genetic screenings of genes contributing to VOC emission, constituting a powerful tool for the functional characterization of VOC biosynthetic genes and elucidation of the biological functions of their products directly in planta.


2019 ◽  
Author(s):  
Huifang Xu ◽  
Weinan Liang ◽  
Linlin Ning ◽  
Yuanyuan Jiang ◽  
Wenxia Yang ◽  
...  

P450 fatty acid decarboxylases (FADCs) have recently been attracting considerable attention owing to their one-step direct production of industrially important 1-alkenes from biologically abundant feedstock free fatty acids under mild conditions. However, attempts to improve the catalytic activity of FADCs have met with little success. Protein engineering has been limited to selected residues and small mutant libraries due to lack of an effective high-throughput screening (HTS) method. Here, we devise a catalase-deficient <i>Escherichia coli</i> host strain and report an HTS approach based on colorimetric detection of H<sub>2</sub>O<sub>2</sub>-consumption activity of FADCs. Directed evolution enabled by this method has led to effective identification for the first time of improved FADC variants for medium-chain 1-alkene production from both DNA shuffling and random mutagenesis libraries. Advantageously, this screening method can be extended to other enzymes that stoichiometrically utilize H<sub>2</sub>O<sub>2</sub> as co-substrate.


2016 ◽  
Vol 101 (3) ◽  
pp. 1063-1072 ◽  
Author(s):  
Chengcheng Yang ◽  
Lidan Ye ◽  
Jiali Gu ◽  
Xiaohong Yang ◽  
Aipeng Li ◽  
...  

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