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Deciphering Ligand Specificity of a Clostridium thermocellum Family 35 Carbohydrate Binding Module (CtCBM35) for Gluco- and Galacto- Substituted Mannans and Its Calcium Induced Stability
This study investigated the role of CBM35 from Clostridium thermocellum (CtCBM35) in polysaccharide recognition. CtCBM35 was cloned into pET28a (+) vector with an engineered His(6) tag and expressed in Escherichia coli BL21 (DE3) cells. A homogenous 15 kDa protein was purified by immobilized metal i...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3855759/ https://www.ncbi.nlm.nih.gov/pubmed/24324599 http://dx.doi.org/10.1371/journal.pone.0080415 |
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author | Ghosh, Arabinda Luís, Ana Sofia Brás, Joana L. A. Pathaw, Neeta Chrungoo, Nikhil K. Fontes, Carlos M. G. A. Goyal, Arun |
author_facet | Ghosh, Arabinda Luís, Ana Sofia Brás, Joana L. A. Pathaw, Neeta Chrungoo, Nikhil K. Fontes, Carlos M. G. A. Goyal, Arun |
author_sort | Ghosh, Arabinda |
collection | PubMed |
description | This study investigated the role of CBM35 from Clostridium thermocellum (CtCBM35) in polysaccharide recognition. CtCBM35 was cloned into pET28a (+) vector with an engineered His(6) tag and expressed in Escherichia coli BL21 (DE3) cells. A homogenous 15 kDa protein was purified by immobilized metal ion chromatography (IMAC). Ligand binding analysis of CtCBM35 was carried out by affinity electrophoresis using various soluble ligands. CtCBM35 showed a manno-configured ligand specific binding displaying significant association with konjac glucomannan (K (a) = 14.3×10(4) M(−1)), carob galactomannan (K (a) = 12.4×10(4) M(−1)) and negligible association (K (a) = 12 µM(−1)) with insoluble mannan. Binding of CtCBM35 with polysaccharides which was calcium dependent exhibited two fold higher association in presence of 10 mM Ca(2+) ion with konjac glucomannan (K (a) = 41×10(4) M(−1)) and carob galactomannan (K (a) = 30×10(4) M(−1)). The polysaccharide binding was further investigated by fluorescence spectrophotometric studies. On binding with carob galactomannan and konjac glucomannan the conformation of CtCBM35 changed significantly with regular 21 nm peak shifts towards lower quantum yield. The degree of association (K (a)) with konjac glucomannan and carob galactomannan, 14.3×10(4) M(−1) and 11.4×10(4) M(−1), respectively, corroborated the findings from affinity electrophoresis. The association of CtCBM35with konjac glucomannan led to higher free energy of binding (ΔG) −25 kJ mole(−1) as compared to carob galactomannan (ΔG) −22 kJ mole(−1). On binding CtCBM35 with konjac glucomannan and carob galactomannan the hydrodynamic radius (R(H)) as analysed by dynamic light scattering (DLS) study, increased to 8 nm and 6 nm, respectively, from 4.25 nm in absence of ligand. The presence of 10 mM Ca(2+) ions imparted stiffer orientation of CtCBM35 particles with increased R(H) of 4.52 nm. Due to such stiffer orientation CtCBM35 became more thermostable and its melting temperature was shifted to 70°C from initial 50°C. |
format | Online Article Text |
id | pubmed-3855759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38557592013-12-09 Deciphering Ligand Specificity of a Clostridium thermocellum Family 35 Carbohydrate Binding Module (CtCBM35) for Gluco- and Galacto- Substituted Mannans and Its Calcium Induced Stability Ghosh, Arabinda Luís, Ana Sofia Brás, Joana L. A. Pathaw, Neeta Chrungoo, Nikhil K. Fontes, Carlos M. G. A. Goyal, Arun PLoS One Research Article This study investigated the role of CBM35 from Clostridium thermocellum (CtCBM35) in polysaccharide recognition. CtCBM35 was cloned into pET28a (+) vector with an engineered His(6) tag and expressed in Escherichia coli BL21 (DE3) cells. A homogenous 15 kDa protein was purified by immobilized metal ion chromatography (IMAC). Ligand binding analysis of CtCBM35 was carried out by affinity electrophoresis using various soluble ligands. CtCBM35 showed a manno-configured ligand specific binding displaying significant association with konjac glucomannan (K (a) = 14.3×10(4) M(−1)), carob galactomannan (K (a) = 12.4×10(4) M(−1)) and negligible association (K (a) = 12 µM(−1)) with insoluble mannan. Binding of CtCBM35 with polysaccharides which was calcium dependent exhibited two fold higher association in presence of 10 mM Ca(2+) ion with konjac glucomannan (K (a) = 41×10(4) M(−1)) and carob galactomannan (K (a) = 30×10(4) M(−1)). The polysaccharide binding was further investigated by fluorescence spectrophotometric studies. On binding with carob galactomannan and konjac glucomannan the conformation of CtCBM35 changed significantly with regular 21 nm peak shifts towards lower quantum yield. The degree of association (K (a)) with konjac glucomannan and carob galactomannan, 14.3×10(4) M(−1) and 11.4×10(4) M(−1), respectively, corroborated the findings from affinity electrophoresis. The association of CtCBM35with konjac glucomannan led to higher free energy of binding (ΔG) −25 kJ mole(−1) as compared to carob galactomannan (ΔG) −22 kJ mole(−1). On binding CtCBM35 with konjac glucomannan and carob galactomannan the hydrodynamic radius (R(H)) as analysed by dynamic light scattering (DLS) study, increased to 8 nm and 6 nm, respectively, from 4.25 nm in absence of ligand. The presence of 10 mM Ca(2+) ions imparted stiffer orientation of CtCBM35 particles with increased R(H) of 4.52 nm. Due to such stiffer orientation CtCBM35 became more thermostable and its melting temperature was shifted to 70°C from initial 50°C. Public Library of Science 2013-12-06 /pmc/articles/PMC3855759/ /pubmed/24324599 http://dx.doi.org/10.1371/journal.pone.0080415 Text en © 2013 Ghosh 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Ghosh, Arabinda Luís, Ana Sofia Brás, Joana L. A. Pathaw, Neeta Chrungoo, Nikhil K. Fontes, Carlos M. G. A. Goyal, Arun Deciphering Ligand Specificity of a Clostridium thermocellum Family 35 Carbohydrate Binding Module (CtCBM35) for Gluco- and Galacto- Substituted Mannans and Its Calcium Induced Stability |
title | Deciphering Ligand Specificity of a Clostridium thermocellum Family 35 Carbohydrate Binding Module (CtCBM35) for Gluco- and Galacto- Substituted Mannans and Its Calcium Induced Stability |
title_full | Deciphering Ligand Specificity of a Clostridium thermocellum Family 35 Carbohydrate Binding Module (CtCBM35) for Gluco- and Galacto- Substituted Mannans and Its Calcium Induced Stability |
title_fullStr | Deciphering Ligand Specificity of a Clostridium thermocellum Family 35 Carbohydrate Binding Module (CtCBM35) for Gluco- and Galacto- Substituted Mannans and Its Calcium Induced Stability |
title_full_unstemmed | Deciphering Ligand Specificity of a Clostridium thermocellum Family 35 Carbohydrate Binding Module (CtCBM35) for Gluco- and Galacto- Substituted Mannans and Its Calcium Induced Stability |
title_short | Deciphering Ligand Specificity of a Clostridium thermocellum Family 35 Carbohydrate Binding Module (CtCBM35) for Gluco- and Galacto- Substituted Mannans and Its Calcium Induced Stability |
title_sort | deciphering ligand specificity of a clostridium thermocellum family 35 carbohydrate binding module (ctcbm35) for gluco- and galacto- substituted mannans and its calcium induced stability |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3855759/ https://www.ncbi.nlm.nih.gov/pubmed/24324599 http://dx.doi.org/10.1371/journal.pone.0080415 |
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