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A highly thermoactive and salt-tolerant α-amylase isolated from a pilot-plant biogas reactor
Aiming at the isolation of novel enzymes from previously uncultured thermophilic microorganisms, a metagenome library was constructed from DNA isolated from a pilot-plant biogas reactor operating at 55 °C. The library was screened for starch-degrading enzymes, and one active clone was found. An open...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602641/ https://www.ncbi.nlm.nih.gov/pubmed/22743714 http://dx.doi.org/10.1007/s00253-012-4194-x |
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author | Jabbour, Dina Sorger, Anneke Sahm, Kerstin Antranikian, Garabed |
author_facet | Jabbour, Dina Sorger, Anneke Sahm, Kerstin Antranikian, Garabed |
author_sort | Jabbour, Dina |
collection | PubMed |
description | Aiming at the isolation of novel enzymes from previously uncultured thermophilic microorganisms, a metagenome library was constructed from DNA isolated from a pilot-plant biogas reactor operating at 55 °C. The library was screened for starch-degrading enzymes, and one active clone was found. An open reading frame of 1,461 bp encoding an α-amylase from an uncultured organism was identified. The amy13A gene was cloned in Escherichia coli, resulting in high-level expression of the recombinant amylase. The novel enzyme Amy13A showed the highest sequence identity (75 %) to α-amylases from Petrotoga mobilis and Halothermothrix orenii. Amy13A is highly thermoactive, exhibiting optimal activity at 80 °C, and it is also highly salt-tolerant, being active in 25 % (w/v) NaCl. Amy13A is one of the few enzymes that tolerate high concentrations of salt and elevated temperatures, making it a potential candidate for starch processing under extreme conditions. |
format | Online Article Text |
id | pubmed-3602641 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-36026412013-03-20 A highly thermoactive and salt-tolerant α-amylase isolated from a pilot-plant biogas reactor Jabbour, Dina Sorger, Anneke Sahm, Kerstin Antranikian, Garabed Appl Microbiol Biotechnol Biotechnologically Relevant Enzymes and Proteins Aiming at the isolation of novel enzymes from previously uncultured thermophilic microorganisms, a metagenome library was constructed from DNA isolated from a pilot-plant biogas reactor operating at 55 °C. The library was screened for starch-degrading enzymes, and one active clone was found. An open reading frame of 1,461 bp encoding an α-amylase from an uncultured organism was identified. The amy13A gene was cloned in Escherichia coli, resulting in high-level expression of the recombinant amylase. The novel enzyme Amy13A showed the highest sequence identity (75 %) to α-amylases from Petrotoga mobilis and Halothermothrix orenii. Amy13A is highly thermoactive, exhibiting optimal activity at 80 °C, and it is also highly salt-tolerant, being active in 25 % (w/v) NaCl. Amy13A is one of the few enzymes that tolerate high concentrations of salt and elevated temperatures, making it a potential candidate for starch processing under extreme conditions. Springer-Verlag 2012-06-29 2013 /pmc/articles/PMC3602641/ /pubmed/22743714 http://dx.doi.org/10.1007/s00253-012-4194-x Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Biotechnologically Relevant Enzymes and Proteins Jabbour, Dina Sorger, Anneke Sahm, Kerstin Antranikian, Garabed A highly thermoactive and salt-tolerant α-amylase isolated from a pilot-plant biogas reactor |
title | A highly thermoactive and salt-tolerant α-amylase isolated from a pilot-plant biogas reactor |
title_full | A highly thermoactive and salt-tolerant α-amylase isolated from a pilot-plant biogas reactor |
title_fullStr | A highly thermoactive and salt-tolerant α-amylase isolated from a pilot-plant biogas reactor |
title_full_unstemmed | A highly thermoactive and salt-tolerant α-amylase isolated from a pilot-plant biogas reactor |
title_short | A highly thermoactive and salt-tolerant α-amylase isolated from a pilot-plant biogas reactor |
title_sort | highly thermoactive and salt-tolerant α-amylase isolated from a pilot-plant biogas reactor |
topic | Biotechnologically Relevant Enzymes and Proteins |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602641/ https://www.ncbi.nlm.nih.gov/pubmed/22743714 http://dx.doi.org/10.1007/s00253-012-4194-x |
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