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Purification and Characterization of a Bifunctional Alginate Lyase from Pseudoalteromonas sp. SM0524
An alginate lyase-producing bacterial strain, Pseudoalteromonas sp. SM0524, was screened from marine rotten kelp. In an optimized condition, the production of alginate lyase from Pseudoalteromonas sp. SM0524 reached 62.6 U/mL, suggesting that strain SM0524 is a good producer of alginate lyases. The...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Molecular Diversity Preservation International
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3039154/ https://www.ncbi.nlm.nih.gov/pubmed/21339950 http://dx.doi.org/10.3390/md9010109 |
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author | Li, Jian-Wei Dong, Sheng Song, Jie Li, Chun-Bo Chen, Xiu-Lan Xie, Bin-Bin Zhang, Yu-Zhong |
author_facet | Li, Jian-Wei Dong, Sheng Song, Jie Li, Chun-Bo Chen, Xiu-Lan Xie, Bin-Bin Zhang, Yu-Zhong |
author_sort | Li, Jian-Wei |
collection | PubMed |
description | An alginate lyase-producing bacterial strain, Pseudoalteromonas sp. SM0524, was screened from marine rotten kelp. In an optimized condition, the production of alginate lyase from Pseudoalteromonas sp. SM0524 reached 62.6 U/mL, suggesting that strain SM0524 is a good producer of alginate lyases. The bifunctional alginate lyase aly-SJ02 secreted by strain SM0524 was purified. Aly-SJ02 had an apparent molecular mass of 32 kDa. The optimal temperature and pH of aly-SJ02 toward sodium alginate was 50 °C and 8.5, respectively. The half life period of aly-SJ02 was 41 min at 40 °C and 20 min at 50 °C. Aly-SJ02 was most stable at pH 8.0. N-terminal sequence analysis suggested that aly-SJ02 may be an alginate lyase of polysaccharide lyase family 18. Aly-SJ02 showed activities toward both polyG (α-l-guluronic acid) and polyM (β-d-mannuronic acid), indicating that it is a bifunctional alginate lyase. Aly-SJ02 had lower K(m) toward polyG than toward polyM and sodium alginate. Thin layer chromatography and ESI-MS analyses showed that aly-SJ02 mainly released dimers and trimers from polyM and alginate, and trimers and tetramers from polyG, which suggests that aly-SJ02 may be a good tool to produce dimers and trimers from alginate. |
format | Text |
id | pubmed-3039154 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Molecular Diversity Preservation International |
record_format | MEDLINE/PubMed |
spelling | pubmed-30391542011-02-18 Purification and Characterization of a Bifunctional Alginate Lyase from Pseudoalteromonas sp. SM0524 Li, Jian-Wei Dong, Sheng Song, Jie Li, Chun-Bo Chen, Xiu-Lan Xie, Bin-Bin Zhang, Yu-Zhong Mar Drugs Article An alginate lyase-producing bacterial strain, Pseudoalteromonas sp. SM0524, was screened from marine rotten kelp. In an optimized condition, the production of alginate lyase from Pseudoalteromonas sp. SM0524 reached 62.6 U/mL, suggesting that strain SM0524 is a good producer of alginate lyases. The bifunctional alginate lyase aly-SJ02 secreted by strain SM0524 was purified. Aly-SJ02 had an apparent molecular mass of 32 kDa. The optimal temperature and pH of aly-SJ02 toward sodium alginate was 50 °C and 8.5, respectively. The half life period of aly-SJ02 was 41 min at 40 °C and 20 min at 50 °C. Aly-SJ02 was most stable at pH 8.0. N-terminal sequence analysis suggested that aly-SJ02 may be an alginate lyase of polysaccharide lyase family 18. Aly-SJ02 showed activities toward both polyG (α-l-guluronic acid) and polyM (β-d-mannuronic acid), indicating that it is a bifunctional alginate lyase. Aly-SJ02 had lower K(m) toward polyG than toward polyM and sodium alginate. Thin layer chromatography and ESI-MS analyses showed that aly-SJ02 mainly released dimers and trimers from polyM and alginate, and trimers and tetramers from polyG, which suggests that aly-SJ02 may be a good tool to produce dimers and trimers from alginate. Molecular Diversity Preservation International 2011-01-21 /pmc/articles/PMC3039154/ /pubmed/21339950 http://dx.doi.org/10.3390/md9010109 Text en © 2011 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Li, Jian-Wei Dong, Sheng Song, Jie Li, Chun-Bo Chen, Xiu-Lan Xie, Bin-Bin Zhang, Yu-Zhong Purification and Characterization of a Bifunctional Alginate Lyase from Pseudoalteromonas sp. SM0524 |
title | Purification and Characterization of a Bifunctional Alginate Lyase from Pseudoalteromonas sp. SM0524 |
title_full | Purification and Characterization of a Bifunctional Alginate Lyase from Pseudoalteromonas sp. SM0524 |
title_fullStr | Purification and Characterization of a Bifunctional Alginate Lyase from Pseudoalteromonas sp. SM0524 |
title_full_unstemmed | Purification and Characterization of a Bifunctional Alginate Lyase from Pseudoalteromonas sp. SM0524 |
title_short | Purification and Characterization of a Bifunctional Alginate Lyase from Pseudoalteromonas sp. SM0524 |
title_sort | purification and characterization of a bifunctional alginate lyase from pseudoalteromonas sp. sm0524 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3039154/ https://www.ncbi.nlm.nih.gov/pubmed/21339950 http://dx.doi.org/10.3390/md9010109 |
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