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Characterisation of three novel α-L-arabinofuranosidases from a compost metagenome
BACKGROUND: The importance of the accessory enzymes such as α-L-arabinofuranosidases (AFases) in synergistic interactions within cellulolytic mixtures has introduced a paradigm shift in the search for hydrolytic enzymes. The aim of this study was to characterize novel AFase genes encoding enzymes wi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6472066/ https://www.ncbi.nlm.nih.gov/pubmed/30999885 http://dx.doi.org/10.1186/s12896-019-0510-1 |
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author | Fortune, Brent Mhlongo, Sizwe van Zyl, Leonardo Joaquim Huddy, Robert Smart, Mariette Trindade, Marla |
author_facet | Fortune, Brent Mhlongo, Sizwe van Zyl, Leonardo Joaquim Huddy, Robert Smart, Mariette Trindade, Marla |
author_sort | Fortune, Brent |
collection | PubMed |
description | BACKGROUND: The importance of the accessory enzymes such as α-L-arabinofuranosidases (AFases) in synergistic interactions within cellulolytic mixtures has introduced a paradigm shift in the search for hydrolytic enzymes. The aim of this study was to characterize novel AFase genes encoding enzymes with differing temperature optima and thermostabilities for use in hydrolytic cocktails. RESULTS: Three fosmids, pFos-H4, E3 and D3 were selected from the cloned metagenome of high temperature compost, expressed in Escherichia coli and subsequently purified to homogeneity from cell lysate. All the AFases were clustered within the GH51 AFase family and shared a homo-hexameric structure. Both AFase-E3 and H4 showed optimal activity at 60 °C while AFase-D3 had unique properties as it showed optimal activity at 25 °C as well as the ability to maintain substantial activity at temperatures as high as 90 °C. However, AFase-E3 was the most thermostable amongst the three AFases showing full activity even at 70 °C. The maximum activity was observed at a pH profile between pH 4.0–6.0 for all three AFases with optimal activity for AFase H4, D3 and E3 at pH 5.0, 4.5 and 4.0, respectively. All the AFases showed K(M) range between 0.31 mM and 0.43 mM, K(cat) range between 131 s(− 1) and 219 s(− 1) and the specific activity for AFase-H4, AFases-E3 and was 143, 228 and 175 U/mg, respectively. AFases-E3 and D3 displayed activities against pNP-β-L-arabinopyranoside and pNP-β-L-mannopyranoside respectively, and both hydrolysed pNP-β-D-glucopyranoside. CONCLUSION: All three AFases displayed different biochemical characteristics despite all showing conserved overall structural similarity with typical domains of AFases belonging to GH51 family. The hydrolysis of cellobiose by a GH51 family AFase is demonstrated for the first time in this study. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12896-019-0510-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6472066 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64720662019-04-24 Characterisation of three novel α-L-arabinofuranosidases from a compost metagenome Fortune, Brent Mhlongo, Sizwe van Zyl, Leonardo Joaquim Huddy, Robert Smart, Mariette Trindade, Marla BMC Biotechnol Research Article BACKGROUND: The importance of the accessory enzymes such as α-L-arabinofuranosidases (AFases) in synergistic interactions within cellulolytic mixtures has introduced a paradigm shift in the search for hydrolytic enzymes. The aim of this study was to characterize novel AFase genes encoding enzymes with differing temperature optima and thermostabilities for use in hydrolytic cocktails. RESULTS: Three fosmids, pFos-H4, E3 and D3 were selected from the cloned metagenome of high temperature compost, expressed in Escherichia coli and subsequently purified to homogeneity from cell lysate. All the AFases were clustered within the GH51 AFase family and shared a homo-hexameric structure. Both AFase-E3 and H4 showed optimal activity at 60 °C while AFase-D3 had unique properties as it showed optimal activity at 25 °C as well as the ability to maintain substantial activity at temperatures as high as 90 °C. However, AFase-E3 was the most thermostable amongst the three AFases showing full activity even at 70 °C. The maximum activity was observed at a pH profile between pH 4.0–6.0 for all three AFases with optimal activity for AFase H4, D3 and E3 at pH 5.0, 4.5 and 4.0, respectively. All the AFases showed K(M) range between 0.31 mM and 0.43 mM, K(cat) range between 131 s(− 1) and 219 s(− 1) and the specific activity for AFase-H4, AFases-E3 and was 143, 228 and 175 U/mg, respectively. AFases-E3 and D3 displayed activities against pNP-β-L-arabinopyranoside and pNP-β-L-mannopyranoside respectively, and both hydrolysed pNP-β-D-glucopyranoside. CONCLUSION: All three AFases displayed different biochemical characteristics despite all showing conserved overall structural similarity with typical domains of AFases belonging to GH51 family. The hydrolysis of cellobiose by a GH51 family AFase is demonstrated for the first time in this study. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12896-019-0510-1) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-18 /pmc/articles/PMC6472066/ /pubmed/30999885 http://dx.doi.org/10.1186/s12896-019-0510-1 Text en © The Author(s). 2019 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Fortune, Brent Mhlongo, Sizwe van Zyl, Leonardo Joaquim Huddy, Robert Smart, Mariette Trindade, Marla Characterisation of three novel α-L-arabinofuranosidases from a compost metagenome |
title | Characterisation of three novel α-L-arabinofuranosidases from a compost metagenome |
title_full | Characterisation of three novel α-L-arabinofuranosidases from a compost metagenome |
title_fullStr | Characterisation of three novel α-L-arabinofuranosidases from a compost metagenome |
title_full_unstemmed | Characterisation of three novel α-L-arabinofuranosidases from a compost metagenome |
title_short | Characterisation of three novel α-L-arabinofuranosidases from a compost metagenome |
title_sort | characterisation of three novel α-l-arabinofuranosidases from a compost metagenome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6472066/ https://www.ncbi.nlm.nih.gov/pubmed/30999885 http://dx.doi.org/10.1186/s12896-019-0510-1 |
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