Determining transaminase activity in bacterial libraries by time-lapse imaging

Transaminase activity was determined by time-lapse imaging using a colourimetric reaction and image analysis. A correlation between the benzaldehyde conversion and relative luminance was determined, allowing the identification of the most promising biocatalysts, the determination of kinetic paramete...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2019-11, Vol.55 (9), p.13538-13541
Hauptverfasser: Rodrigues, Carlos J. C, Sanches, João M, de Carvalho, Carla C. C. R
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creator Rodrigues, Carlos J. C
Sanches, João M
de Carvalho, Carla C. C. R
description Transaminase activity was determined by time-lapse imaging using a colourimetric reaction and image analysis. A correlation between the benzaldehyde conversion and relative luminance was determined, allowing the identification of the most promising biocatalysts, the determination of kinetic parameters, and the assessment of the effect of the substrate concentration on activity. Transaminase activity was determined by time-lapse imaging using a colourimetric reaction and image analysis. The correlation between substrate concentration and luminance allows the screening of biocatalysts and determination of kinetic parameters.
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source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
subjects Benzaldehyde
Correlation analysis
Image analysis
Parameter identification
Substrates
title Determining transaminase activity in bacterial libraries by time-lapse imaging
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