Journal
JOURNAL OF BIOTECHNOLOGY
Volume 147, Issue 3-4, Pages 164-168Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.jbiotec.2010.04.002
Keywords
Calorimetric assay; pH indicator; Microplate format; Halohydrin dehalogenase; High throughput screening
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Funding
- National Natural Science Foundation of China [20872014]
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Here we have reported a high throughput pH indicator-based assay to measure the activity of halohydrin dehalogenases (HheC). The assay relies upon the absorbance change at 560 nm and the visual color change of phenol red in a weakly buffered system, due to the release of protons from the enzyme-catalyzed ring-closure reactions. The assay can be performed in a microplate format using whole cells, making the assay simple and robust. Thus, it is suitable for library screening. The assay has been further validated using two previously studied HheC variants, D8ON and W249F, which exhibit 200-fold lower and 2-fold higher k(cat) values, respectively, toward 1,3-dichloro-2-propanol than the wild-type HheC. In addition, a saturation mutagenesis library of HheC was screened using the developed assay for its ability to efficiently catalyze the conversion of 1,3-dichloro-2-propanol. After screening of 500 colonies, one mutant W139C was identified and was further purified and characterized. Kinetic analysis indicates that the resulting mutant shows 2- and 5-fold improvement in k(cat) value toward 1,3-DCP and (R,S)-p-nitro-2bromo-1-phenylethanol, respectively, although it exhibits higher K(m), values than the wild-type enzyme. The method described herein represents a useful tool given the need for the high throughput screening of halohydrin dehalogenase mutants. (C) 2010 Elsevier B.V. All rights reserved.
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