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3,4-Dihydroxyphenylacetate 2,3-dioxygenase from Pseudomonas aeruginosa: An Fe(II)-containing enzyme with fast turnover

3,4-dihydroxyphenylacetate (DHPA) dioxygenase (DHPAO) from Pseudomonas aeruginosa (PaDHPAO) was overexpressed in Escherichia coli and purified to homogeneity. As the enzyme lost activity over time, a protocol to reactivate and conserve PaDHPAO activity has been developed. Addition of Fe(II), DTT and...

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Autores principales: Pornsuwan, Soraya, Maenpuen, Somchart, Kamutira, Philaiwarong, Watthaisong, Pratchaya, Thotsaporn, Kittisak, Tongsook, Chanakan, Juttulapa, Maneerat, Nijvipakul, Sarayut, Chaiyen, Pimchai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5291488/
https://www.ncbi.nlm.nih.gov/pubmed/28158217
http://dx.doi.org/10.1371/journal.pone.0171135
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author Pornsuwan, Soraya
Maenpuen, Somchart
Kamutira, Philaiwarong
Watthaisong, Pratchaya
Thotsaporn, Kittisak
Tongsook, Chanakan
Juttulapa, Maneerat
Nijvipakul, Sarayut
Chaiyen, Pimchai
author_facet Pornsuwan, Soraya
Maenpuen, Somchart
Kamutira, Philaiwarong
Watthaisong, Pratchaya
Thotsaporn, Kittisak
Tongsook, Chanakan
Juttulapa, Maneerat
Nijvipakul, Sarayut
Chaiyen, Pimchai
author_sort Pornsuwan, Soraya
collection PubMed
description 3,4-dihydroxyphenylacetate (DHPA) dioxygenase (DHPAO) from Pseudomonas aeruginosa (PaDHPAO) was overexpressed in Escherichia coli and purified to homogeneity. As the enzyme lost activity over time, a protocol to reactivate and conserve PaDHPAO activity has been developed. Addition of Fe(II), DTT and ascorbic acid or ROS scavenging enzymes (catalase or superoxide dismutase) was required to preserve enzyme stability. Metal content and activity analyses indicated that PaDHPAO uses Fe(II) as a metal cofactor. NMR analysis of the reaction product indicated that PaDHPAO catalyzes the 2,3-extradiol ring-cleavage of DHPA to form 5-carboxymethyl-2-hydroxymuconate semialdehyde (CHMS) which has a molar absorptivity of 32.23 mM(-1)cm(-1) at 380 nm and pH 7.5. Steady-state kinetics under air-saturated conditions at 25°C and pH 7.5 showed a K(m) for DHPA of 58 ± 8 μM and a k(cat) of 64 s(-1), indicating that the turnover of PaDHPAO is relatively fast compared to other DHPAOs. The pH-rate profile of the PaDHPAO reaction shows a bell-shaped plot that exhibits a maximum activity at pH 7.5 with two pK(a) values of 6.5 ± 0.1 and 8.9 ± 0.1. Study of the effect of temperature on PaDHPAO activity indicated that the enzyme activity increases as temperature increases up to 55°C. The Arrhenius plot of ln(k’(cat)) versus the reciprocal of the absolute temperature shows two correlations with a transition temperature at 35°C. Two activation energy values (E(a)) above and below the transition temperature were calculated as 42 and 14 kJ/mol, respectively. The data imply that the rate determining steps of the PaDHPAO reaction at temperatures above and below 35°C may be different. Sequence similarity network analysis indicated that PaDHPAO belongs to the enzyme clusters that are largely unexplored. As PaDHPAO has a high turnover number compared to most of the enzymes previously reported, understanding its biochemical and biophysical properties should be useful for future applications in biotechnology.
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spelling pubmed-52914882017-02-17 3,4-Dihydroxyphenylacetate 2,3-dioxygenase from Pseudomonas aeruginosa: An Fe(II)-containing enzyme with fast turnover Pornsuwan, Soraya Maenpuen, Somchart Kamutira, Philaiwarong Watthaisong, Pratchaya Thotsaporn, Kittisak Tongsook, Chanakan Juttulapa, Maneerat Nijvipakul, Sarayut Chaiyen, Pimchai PLoS One Research Article 3,4-dihydroxyphenylacetate (DHPA) dioxygenase (DHPAO) from Pseudomonas aeruginosa (PaDHPAO) was overexpressed in Escherichia coli and purified to homogeneity. As the enzyme lost activity over time, a protocol to reactivate and conserve PaDHPAO activity has been developed. Addition of Fe(II), DTT and ascorbic acid or ROS scavenging enzymes (catalase or superoxide dismutase) was required to preserve enzyme stability. Metal content and activity analyses indicated that PaDHPAO uses Fe(II) as a metal cofactor. NMR analysis of the reaction product indicated that PaDHPAO catalyzes the 2,3-extradiol ring-cleavage of DHPA to form 5-carboxymethyl-2-hydroxymuconate semialdehyde (CHMS) which has a molar absorptivity of 32.23 mM(-1)cm(-1) at 380 nm and pH 7.5. Steady-state kinetics under air-saturated conditions at 25°C and pH 7.5 showed a K(m) for DHPA of 58 ± 8 μM and a k(cat) of 64 s(-1), indicating that the turnover of PaDHPAO is relatively fast compared to other DHPAOs. The pH-rate profile of the PaDHPAO reaction shows a bell-shaped plot that exhibits a maximum activity at pH 7.5 with two pK(a) values of 6.5 ± 0.1 and 8.9 ± 0.1. Study of the effect of temperature on PaDHPAO activity indicated that the enzyme activity increases as temperature increases up to 55°C. The Arrhenius plot of ln(k’(cat)) versus the reciprocal of the absolute temperature shows two correlations with a transition temperature at 35°C. Two activation energy values (E(a)) above and below the transition temperature were calculated as 42 and 14 kJ/mol, respectively. The data imply that the rate determining steps of the PaDHPAO reaction at temperatures above and below 35°C may be different. Sequence similarity network analysis indicated that PaDHPAO belongs to the enzyme clusters that are largely unexplored. As PaDHPAO has a high turnover number compared to most of the enzymes previously reported, understanding its biochemical and biophysical properties should be useful for future applications in biotechnology. Public Library of Science 2017-02-03 /pmc/articles/PMC5291488/ /pubmed/28158217 http://dx.doi.org/10.1371/journal.pone.0171135 Text en © 2017 Pornsuwan et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Pornsuwan, Soraya
Maenpuen, Somchart
Kamutira, Philaiwarong
Watthaisong, Pratchaya
Thotsaporn, Kittisak
Tongsook, Chanakan
Juttulapa, Maneerat
Nijvipakul, Sarayut
Chaiyen, Pimchai
3,4-Dihydroxyphenylacetate 2,3-dioxygenase from Pseudomonas aeruginosa: An Fe(II)-containing enzyme with fast turnover
title 3,4-Dihydroxyphenylacetate 2,3-dioxygenase from Pseudomonas aeruginosa: An Fe(II)-containing enzyme with fast turnover
title_full 3,4-Dihydroxyphenylacetate 2,3-dioxygenase from Pseudomonas aeruginosa: An Fe(II)-containing enzyme with fast turnover
title_fullStr 3,4-Dihydroxyphenylacetate 2,3-dioxygenase from Pseudomonas aeruginosa: An Fe(II)-containing enzyme with fast turnover
title_full_unstemmed 3,4-Dihydroxyphenylacetate 2,3-dioxygenase from Pseudomonas aeruginosa: An Fe(II)-containing enzyme with fast turnover
title_short 3,4-Dihydroxyphenylacetate 2,3-dioxygenase from Pseudomonas aeruginosa: An Fe(II)-containing enzyme with fast turnover
title_sort 3,4-dihydroxyphenylacetate 2,3-dioxygenase from pseudomonas aeruginosa: an fe(ii)-containing enzyme with fast turnover
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5291488/
https://www.ncbi.nlm.nih.gov/pubmed/28158217
http://dx.doi.org/10.1371/journal.pone.0171135
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