A Liquid-Based Colorimetric Assay of Lysine Decarboxylase and Its Application to Enzymatic Assay
0
조회
0
다운로드
2
인용
0
참고문헌
키워드
초록
A liquid-based colorimetric assay using a pH indicator was introduced for high-throughput monitoring of lysine decarboxylase activity. The assay is based on the color change of bromocresol purple, measured at 595 nm in liquid reaction mixture, due to an increase of pH by the production of cadaverine. Bromocresol purple was selected as the indicator because it has higher sensitivity than bromothymol blue and pheonol red within a broad range and shows good linearity within the applied pH. We applied this for simple determination of lysine decarboxylase reusability using 96-well plates, and optimization of conditions for enzyme overexpression with different concentrations of IPTG on lysine decarboxylase. This assay is expected to be applied for monitoring and quantifying the liquid-based enzyme reaction in biotransformation of decarboxylase in a high-throughput way.
Abstract
A liquid-based colorimetric assay using a pH indicator was introduced for high-throughput monitoring of lysine decarboxylase activity. The assay is based on the color change of bromocresol purple, measured at 595 nm in liquid reaction mixture, due to an increase of pH by the production of cadaverine. Bromocresol purple was selected as the indicator because it has higher sensitivity than bromothymol blue and pheonol red within a broad range and shows good linearity within the applied pH. We applied this for simple determination of lysine decarboxylase reusability using 96-well plates, and optimization of conditions for enzyme overexpression with different concentrations of IPTG on lysine decarboxylase. This assay is expected to be applied for monitoring and quantifying the liquid-based enzyme reaction in biotransformation of decarboxylase in a high-throughput way.
참고문헌 (14)
- Banerjee A, "A highthroughput amenable colorimetric assay for enantioselective screening of nitrilase-producing microorganisms using pH sensitive indicators", J. Biomol. Screen, 8, pp.559~565 (2003)
- Bhatia SK, "Starch-based polyhydroxybutyrate production in engineered Escherichia coli", Bioprocess Biosyst Eng, 38, pp.1479~1484 (2015)
- Bover-Cid S, "Improved screening procedure for biogenic amine production by lactic acid bacteria", Int. J. Food Microbiol, 53, pp.33~41 (1999)
- Brooker DC, "Rapid test for lysine decarboxylase activity in Enterobacteriaceae", Appl. Microbiol, 26, pp.622~623 (1973)
- Flores HE, "Analysis of polyamines in higher plants by high performance liquid chromatography", Plant Physiol, 69, pp.701~706 (1982)
- Goldschmidt MC, "Rapid methods for determining decarboxylase activity: ornithine and lysine decarboxylases", Appl. Microbiol, 22, pp.344~349 (1971)
- Janne J, "Dissociation of putrescineactivated decarboxylation of S-adenosyl-L-methionine from the enzymic synthesis of spermidine and spermine by purified prostatic enzyme preparations", Biochem. Biophys. Res. Commun, 42, pp.222~229 (1971)
- 김현중, "Optimization of Direct Lysine Decarboxylase Biotransformation for Cadaverine Production with Whole-Cell Biocatalysts at High Lysine Concentration", Journal of Microbiology and Biotechnology, 25(7), pp.1108~1113 (2015), 한국미생물·생명공학회[DOI]
- Kim YH, "Application of diethyl ethoxymethylenemalonate (DEEMM) derivatization for monitoring of lysine decarboxylase activity", J. Mol. Catal. B Enzym, 115, pp.151~154 (2015)
- Kind S, "Bio-based production of the platform chemical 1,5-diaminopentane", Appl. Microbiol. Biotechnol, 91, pp.1287~1296 (2011)
- Knapp DR, "Handbook of Analytical of Derivatization Reactions", pp.6~ (1979), John Wiley & Sons
- Kvannes J, "Rapid and sensitive assay of ornithine decarboxylase activity by high-performance liquid chromatography of the o-phthalaldehyde derivative of putrescine", J. Chromatogr, 419, pp.291~295 (1987)
- Phan AP, "Spectrophotometric assay for lysine decarboxylase", Anal. Biochem, 120, pp.193~197 (1982)
- Yang YH, "Biosynthesis of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) containing a predominant amount of 3-hydroxyvalerate by engineered Escherichia coli expressing propionate-CoA transferase", J. Appl. Microbiol, 113, pp.815~823 (2012)
