Dataset of the characterization of the optimum pH of reaction, optimum cofactor concentration, optimum initial enzymatic activities and ratios and the use of a sparging gas for the multi-enzymatic synthesis of acetoin from ethanol in a one-pot reactor.
METHODOLOGICAL INFORMATION
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Description of the methods used to collect and generate the data:
-Single enzymatic reaction (ZpPDC) and preliminary characterizations (ZpPDC/ScADH and ZpPDC/ScADH/SpNOX) were carried out in 50 mL using tris base buffer at different pH conditions, acetaldehyde or etanol 50 mM, at 25ºC and 500 rpm.
-Multi-enzymatic system reaction was carried out in 5 mL using tris base buffer pH 7.5 and bioetanol 50 mM, with pH control, at 25ºC, 1000 rpm and 1 vvm of air.
-Activities were obtained applying activity tests based on spectrophotometrical methods.
-GC for the analysis of ethanol, acetaldehyde and acetoin concentration.
-Protein purification was carried out in a FPLC AKTA Pure System.
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Data processing methods:
All data were processed using Excel
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Software or instruments needed to interpret the data:
Excel
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Information about instruments, calibration and standards:
- Varian Cary 50 Bio UV-visible spectrophotometer (Agilent®).
- FPLC
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GC
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Environmental or experimental conditions:
Atmospheric pressure and 25ºC.