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Cloning, Expression and Biochemical Characterization of Endomannanases from Thermobifida Species Isolated from Different Niches
Thermobifidas are thermotolerant, compost inhabiting actinomycetes which have complex polysaccharide hydrolyzing enzyme systems. The best characterized enzymes of these hydrolases are cellulases from T. fusca, while other important enzymes especially hemicellulases are not deeply explored. To fill t...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4880297/ https://www.ncbi.nlm.nih.gov/pubmed/27223892 http://dx.doi.org/10.1371/journal.pone.0155769 |
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author | Tóth, Ákos Barna, Terézia Szabó, Erna Elek, Rita Hubert, Ágnes Nagy, István Nagy, István Kriszt, Balázs Táncsics, András Kukolya, József |
author_facet | Tóth, Ákos Barna, Terézia Szabó, Erna Elek, Rita Hubert, Ágnes Nagy, István Nagy, István Kriszt, Balázs Táncsics, András Kukolya, József |
author_sort | Tóth, Ákos |
collection | PubMed |
description | Thermobifidas are thermotolerant, compost inhabiting actinomycetes which have complex polysaccharide hydrolyzing enzyme systems. The best characterized enzymes of these hydrolases are cellulases from T. fusca, while other important enzymes especially hemicellulases are not deeply explored. To fill this gap we cloned and investigated endomannanases from those reference strains of the Thermobifida genus, which have published data on other hydrolases (T. fusca TM51, T. alba CECT3323, T. cellulosilytica TB100(T) and T. halotolerans YIM90462(T)). Our phylogenetic analyses of 16S rDNA and endomannanase sequences revealed that T. alba CECT3323 is miss-classified; it belongs to the T. fusca species. The cloned and investigated endomannanases belong to the family of glycosyl hydrolases 5 (GH5), their size is around 50 kDa and they are modular enzymes. Their catalytic domains are extended by a C-terminal carbohydrate binding module (CBM) of type 2 with a 23–25 residues long interdomain linker region consisting of Pro, Thr and Glu/Asp rich repetitive tetrapeptide motifs. Their polypeptide chains exhibit high homology, interdomain sequence, which don’t show homology to each other, but all of them are built up from 3–6 times repeated tetrapeptide motifs) (PTDP-Tc, TEEP-Tf, DPGT-Th). All of the heterologously expressed Man5A enzymes exhibited activity only on mannan. The pH optima of Man5A enzymes from T. halotolerans, T. cellulosilytica and T. fusca are slightly different (7.0, 7.5 and 8.0, respectively) while their temperature optima span within the range of 70–75°C. The three endomannanases exhibited very similar kinetic performances on LBG-mannan substrate: 0.9–1.7mM of K(M) and 80–120 1/sec of turnover number. We detected great variability in heat stability at 70°C, which was influenced by the presence of Ca(2+). The investigated endomannanases might be important subjects for studying the structure/function relation behind the heat stability and for industrial applications to hemicellulose degradation. |
format | Online Article Text |
id | pubmed-4880297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-48802972016-06-09 Cloning, Expression and Biochemical Characterization of Endomannanases from Thermobifida Species Isolated from Different Niches Tóth, Ákos Barna, Terézia Szabó, Erna Elek, Rita Hubert, Ágnes Nagy, István Nagy, István Kriszt, Balázs Táncsics, András Kukolya, József PLoS One Research Article Thermobifidas are thermotolerant, compost inhabiting actinomycetes which have complex polysaccharide hydrolyzing enzyme systems. The best characterized enzymes of these hydrolases are cellulases from T. fusca, while other important enzymes especially hemicellulases are not deeply explored. To fill this gap we cloned and investigated endomannanases from those reference strains of the Thermobifida genus, which have published data on other hydrolases (T. fusca TM51, T. alba CECT3323, T. cellulosilytica TB100(T) and T. halotolerans YIM90462(T)). Our phylogenetic analyses of 16S rDNA and endomannanase sequences revealed that T. alba CECT3323 is miss-classified; it belongs to the T. fusca species. The cloned and investigated endomannanases belong to the family of glycosyl hydrolases 5 (GH5), their size is around 50 kDa and they are modular enzymes. Their catalytic domains are extended by a C-terminal carbohydrate binding module (CBM) of type 2 with a 23–25 residues long interdomain linker region consisting of Pro, Thr and Glu/Asp rich repetitive tetrapeptide motifs. Their polypeptide chains exhibit high homology, interdomain sequence, which don’t show homology to each other, but all of them are built up from 3–6 times repeated tetrapeptide motifs) (PTDP-Tc, TEEP-Tf, DPGT-Th). All of the heterologously expressed Man5A enzymes exhibited activity only on mannan. The pH optima of Man5A enzymes from T. halotolerans, T. cellulosilytica and T. fusca are slightly different (7.0, 7.5 and 8.0, respectively) while their temperature optima span within the range of 70–75°C. The three endomannanases exhibited very similar kinetic performances on LBG-mannan substrate: 0.9–1.7mM of K(M) and 80–120 1/sec of turnover number. We detected great variability in heat stability at 70°C, which was influenced by the presence of Ca(2+). The investigated endomannanases might be important subjects for studying the structure/function relation behind the heat stability and for industrial applications to hemicellulose degradation. Public Library of Science 2016-05-25 /pmc/articles/PMC4880297/ /pubmed/27223892 http://dx.doi.org/10.1371/journal.pone.0155769 Text en © 2016 Tóth et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Tóth, Ákos Barna, Terézia Szabó, Erna Elek, Rita Hubert, Ágnes Nagy, István Nagy, István Kriszt, Balázs Táncsics, András Kukolya, József Cloning, Expression and Biochemical Characterization of Endomannanases from Thermobifida Species Isolated from Different Niches |
title | Cloning, Expression and Biochemical Characterization of Endomannanases from Thermobifida Species Isolated from Different Niches |
title_full | Cloning, Expression and Biochemical Characterization of Endomannanases from Thermobifida Species Isolated from Different Niches |
title_fullStr | Cloning, Expression and Biochemical Characterization of Endomannanases from Thermobifida Species Isolated from Different Niches |
title_full_unstemmed | Cloning, Expression and Biochemical Characterization of Endomannanases from Thermobifida Species Isolated from Different Niches |
title_short | Cloning, Expression and Biochemical Characterization of Endomannanases from Thermobifida Species Isolated from Different Niches |
title_sort | cloning, expression and biochemical characterization of endomannanases from thermobifida species isolated from different niches |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4880297/ https://www.ncbi.nlm.nih.gov/pubmed/27223892 http://dx.doi.org/10.1371/journal.pone.0155769 |
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