Extracellular Polyhydroxyalkanoate Depolymerase by Acidovorax sp. DP5

Bacteria capable of degrading polyhydroxyalkanoates (PHA) by secreting extracellular depolymerase enzymes were isolated from water and soil samples collected fromvarious environments in Malaysia. A total of 8 potential degraders exhibited clear zones on poly(3-hydroxybutyrate) [P(3HB)] based agar,...

Full description

Saved in:
Bibliographic Details
Main Authors: Vigneswari, S., Lee, T. S., Bhubalan, Kesaven, Amirul, A. A.
Format: Article
Language:English
Published: Hindawi Publishing Corporation 2015
Subjects:
Online Access:http://eprints.usm.my/39096/1/Extracellular_Polyhydroxyalkanoate_Depolymerase_by_Acidovorax_sp._DP5.pdf
http://eprints.usm.my/39096/
http://dx.doi.org/10.1155/2015/212159
Tags: Add Tag
No Tags, Be the first to tag this record!
id my.usm.eprints.39096
record_format eprints
spelling my.usm.eprints.39096 http://eprints.usm.my/39096/ Extracellular Polyhydroxyalkanoate Depolymerase by Acidovorax sp. DP5 Vigneswari, S. Lee, T. S. Bhubalan, Kesaven Amirul, A. A. QH1 Natural history (General - Including nature conservation, geographical distribution) Bacteria capable of degrading polyhydroxyalkanoates (PHA) by secreting extracellular depolymerase enzymes were isolated from water and soil samples collected fromvarious environments in Malaysia. A total of 8 potential degraders exhibited clear zones on poly(3-hydroxybutyrate) [P(3HB)] based agar, indicating the presence of extracellular PHAdepolymerase.Among the isolates,DP5 exhibited the largest clearing zone with a degradation index of 6.0. The highest degradation activity of P(3HB) was also observed with depolymerase enzyme of DP5 in mineral salt medium containing P(3HB). Based on biochemical characterization and 16S rRNA cloning and sequencing, isolate DP5 was found to belong to the genus Acidovorax and subsequently named as Acidovorax sp. DP5.The highest extracellular depolymerase enzyme activity was achieved when 0.25% (w/v) of P(3HB) and 1 g/L of urea were used as carbon and nitrogen source, respectively, in the culture media. The most suitable assay condition of the depolymerase enzyme in response to pH and temperature was tested. The depolymerase produced by strain Acidovorax sp. DP5 showed high percentage of degradation with P(3HB) films in an alkaline condition with pH 9 and at a temperature of 40∘C. Hindawi Publishing Corporation 2015 Article PeerReviewed application/pdf en http://eprints.usm.my/39096/1/Extracellular_Polyhydroxyalkanoate_Depolymerase_by_Acidovorax_sp._DP5.pdf Vigneswari, S. and Lee, T. S. and Bhubalan, Kesaven and Amirul, A. A. (2015) Extracellular Polyhydroxyalkanoate Depolymerase by Acidovorax sp. DP5. Enzyme Research, 2015 (212159). pp. 1-8. ISSN 2090-0406 http://dx.doi.org/10.1155/2015/212159
institution Universiti Sains Malaysia
building Hamzah Sendut Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Sains Malaysia
content_source USM Institutional Repository
url_provider http://eprints.usm.my/
language English
topic QH1 Natural history (General - Including nature conservation, geographical distribution)
spellingShingle QH1 Natural history (General - Including nature conservation, geographical distribution)
Vigneswari, S.
Lee, T. S.
Bhubalan, Kesaven
Amirul, A. A.
Extracellular Polyhydroxyalkanoate Depolymerase by Acidovorax sp. DP5
description Bacteria capable of degrading polyhydroxyalkanoates (PHA) by secreting extracellular depolymerase enzymes were isolated from water and soil samples collected fromvarious environments in Malaysia. A total of 8 potential degraders exhibited clear zones on poly(3-hydroxybutyrate) [P(3HB)] based agar, indicating the presence of extracellular PHAdepolymerase.Among the isolates,DP5 exhibited the largest clearing zone with a degradation index of 6.0. The highest degradation activity of P(3HB) was also observed with depolymerase enzyme of DP5 in mineral salt medium containing P(3HB). Based on biochemical characterization and 16S rRNA cloning and sequencing, isolate DP5 was found to belong to the genus Acidovorax and subsequently named as Acidovorax sp. DP5.The highest extracellular depolymerase enzyme activity was achieved when 0.25% (w/v) of P(3HB) and 1 g/L of urea were used as carbon and nitrogen source, respectively, in the culture media. The most suitable assay condition of the depolymerase enzyme in response to pH and temperature was tested. The depolymerase produced by strain Acidovorax sp. DP5 showed high percentage of degradation with P(3HB) films in an alkaline condition with pH 9 and at a temperature of 40∘C.
format Article
author Vigneswari, S.
Lee, T. S.
Bhubalan, Kesaven
Amirul, A. A.
author_facet Vigneswari, S.
Lee, T. S.
Bhubalan, Kesaven
Amirul, A. A.
author_sort Vigneswari, S.
title Extracellular Polyhydroxyalkanoate Depolymerase by Acidovorax sp. DP5
title_short Extracellular Polyhydroxyalkanoate Depolymerase by Acidovorax sp. DP5
title_full Extracellular Polyhydroxyalkanoate Depolymerase by Acidovorax sp. DP5
title_fullStr Extracellular Polyhydroxyalkanoate Depolymerase by Acidovorax sp. DP5
title_full_unstemmed Extracellular Polyhydroxyalkanoate Depolymerase by Acidovorax sp. DP5
title_sort extracellular polyhydroxyalkanoate depolymerase by acidovorax sp. dp5
publisher Hindawi Publishing Corporation
publishDate 2015
url http://eprints.usm.my/39096/1/Extracellular_Polyhydroxyalkanoate_Depolymerase_by_Acidovorax_sp._DP5.pdf
http://eprints.usm.my/39096/
http://dx.doi.org/10.1155/2015/212159
_version_ 1643709551360344064
score 13.211869