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Novel archaeal thermostable cellulases from an oil reservoir metagenome

Microbial assemblages were sampled from an offshore deep sub-surface petroleum reservoir 2.5 km below the ocean floor off the coast of Norway, providing conditions of high temperature and pressure, to identify new thermostable enzymes. In this study, we used DNA sequences obtained directly from the...

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Autores principales: Lewin, Anna, Zhou, Jinglie, Pham, Vu Thuy Trang, Haugen, Tone, Zeiny, Mohamed El, Aarstad, Olav, Liebl, Wolfgang, Wentzel, Alexander, Liles, Mark R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5622026/
https://www.ncbi.nlm.nih.gov/pubmed/28963711
http://dx.doi.org/10.1186/s13568-017-0485-z
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author Lewin, Anna
Zhou, Jinglie
Pham, Vu Thuy Trang
Haugen, Tone
Zeiny, Mohamed El
Aarstad, Olav
Liebl, Wolfgang
Wentzel, Alexander
Liles, Mark R.
author_facet Lewin, Anna
Zhou, Jinglie
Pham, Vu Thuy Trang
Haugen, Tone
Zeiny, Mohamed El
Aarstad, Olav
Liebl, Wolfgang
Wentzel, Alexander
Liles, Mark R.
author_sort Lewin, Anna
collection PubMed
description Microbial assemblages were sampled from an offshore deep sub-surface petroleum reservoir 2.5 km below the ocean floor off the coast of Norway, providing conditions of high temperature and pressure, to identify new thermostable enzymes. In this study, we used DNA sequences obtained directly from the sample metagenome and from a derived fosmid library to survey the functional diversity of this extreme habitat. The metagenomic fosmid library containing 11,520 clones was screened using function- and sequence-based methods to identify recombinant clones expressing carbohydrate-degrading enzymes. Open reading frames (ORFs) encoding carbohydrate-degrading enzymes were predicted by BLAST against the CAZy database, and many fosmid clones expressing carbohydrate-degrading activities were discovered by functional screening using Escherichia coli as a heterologous host. Each complete ORF predicted to encode a cellulase identified from sequence- or function-based screening was subcloned in an expression vector. Five subclones was found to have significant activity using a fluorescent cellulose model substrate, and three of these were observed to be highly thermostable. Based on phylogenetic analyses, the thermostable cellulases were derived from thermophilic Archaea and are distinct from known cellulases. Cellulase F1, obtained from function-based screening, contains two distinct cellulase modules, perhaps resulting from fusion of two archaeal cellulases and with a novel protein structure that may result in enhanced activity and thermostability. This enzyme was found to exhibit exocellulase function and to have a remarkably high activity compared to commercially available enzymes. Results from this study highlight the complementarity of hybrid approaches for enzyme discovery, combining sequence- and function-based screening. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13568-017-0485-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-56220262017-10-13 Novel archaeal thermostable cellulases from an oil reservoir metagenome Lewin, Anna Zhou, Jinglie Pham, Vu Thuy Trang Haugen, Tone Zeiny, Mohamed El Aarstad, Olav Liebl, Wolfgang Wentzel, Alexander Liles, Mark R. AMB Express Original Article Microbial assemblages were sampled from an offshore deep sub-surface petroleum reservoir 2.5 km below the ocean floor off the coast of Norway, providing conditions of high temperature and pressure, to identify new thermostable enzymes. In this study, we used DNA sequences obtained directly from the sample metagenome and from a derived fosmid library to survey the functional diversity of this extreme habitat. The metagenomic fosmid library containing 11,520 clones was screened using function- and sequence-based methods to identify recombinant clones expressing carbohydrate-degrading enzymes. Open reading frames (ORFs) encoding carbohydrate-degrading enzymes were predicted by BLAST against the CAZy database, and many fosmid clones expressing carbohydrate-degrading activities were discovered by functional screening using Escherichia coli as a heterologous host. Each complete ORF predicted to encode a cellulase identified from sequence- or function-based screening was subcloned in an expression vector. Five subclones was found to have significant activity using a fluorescent cellulose model substrate, and three of these were observed to be highly thermostable. Based on phylogenetic analyses, the thermostable cellulases were derived from thermophilic Archaea and are distinct from known cellulases. Cellulase F1, obtained from function-based screening, contains two distinct cellulase modules, perhaps resulting from fusion of two archaeal cellulases and with a novel protein structure that may result in enhanced activity and thermostability. This enzyme was found to exhibit exocellulase function and to have a remarkably high activity compared to commercially available enzymes. Results from this study highlight the complementarity of hybrid approaches for enzyme discovery, combining sequence- and function-based screening. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13568-017-0485-z) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2017-09-29 /pmc/articles/PMC5622026/ /pubmed/28963711 http://dx.doi.org/10.1186/s13568-017-0485-z Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Lewin, Anna
Zhou, Jinglie
Pham, Vu Thuy Trang
Haugen, Tone
Zeiny, Mohamed El
Aarstad, Olav
Liebl, Wolfgang
Wentzel, Alexander
Liles, Mark R.
Novel archaeal thermostable cellulases from an oil reservoir metagenome
title Novel archaeal thermostable cellulases from an oil reservoir metagenome
title_full Novel archaeal thermostable cellulases from an oil reservoir metagenome
title_fullStr Novel archaeal thermostable cellulases from an oil reservoir metagenome
title_full_unstemmed Novel archaeal thermostable cellulases from an oil reservoir metagenome
title_short Novel archaeal thermostable cellulases from an oil reservoir metagenome
title_sort novel archaeal thermostable cellulases from an oil reservoir metagenome
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5622026/
https://www.ncbi.nlm.nih.gov/pubmed/28963711
http://dx.doi.org/10.1186/s13568-017-0485-z
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