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Intrinsic Levanase Activity of Bacillus subtilis 168 Levansucrase (SacB)
Levansucrase catalyzes the synthesis of fructose polymers through the transfer of fructosyl units from sucrose to a growing fructan chain. Levanase activity of Bacillus subtilis levansucrase has been described since the very first publications dealing with the mechanism of levan synthesis. However,...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4658133/ https://www.ncbi.nlm.nih.gov/pubmed/26600431 http://dx.doi.org/10.1371/journal.pone.0143394 |
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author | Méndez-Lorenzo, Luz Porras-Domínguez, Jaime R. Raga-Carbajal, Enrique Olvera, Clarita Rodríguez-Alegría, Maria Elena Carrillo-Nava, Ernesto Costas, Miguel López Munguía, Agustín |
author_facet | Méndez-Lorenzo, Luz Porras-Domínguez, Jaime R. Raga-Carbajal, Enrique Olvera, Clarita Rodríguez-Alegría, Maria Elena Carrillo-Nava, Ernesto Costas, Miguel López Munguía, Agustín |
author_sort | Méndez-Lorenzo, Luz |
collection | PubMed |
description | Levansucrase catalyzes the synthesis of fructose polymers through the transfer of fructosyl units from sucrose to a growing fructan chain. Levanase activity of Bacillus subtilis levansucrase has been described since the very first publications dealing with the mechanism of levan synthesis. However, there is a lack of qualitative and quantitative evidence regarding the importance of the intrinsic levan hydrolysis of B. subtilis levansucrase and its role in the levan synthesis process. Particularly, little attention has been paid to the long-term hydrolysis products, including its participation in the final levan molecules distribution. Here, we explored the hydrolytic and transferase activity of the B. subtilis levansucrase (SacB) when levans produced by the same enzyme are used as substrate. We found that levan is hydrolyzed through a first order exo-type mechanism, which is limited to a conversion extent of around 30% when all polymer molecules reach a structure no longer suitable to SacB hydrolysis. To characterize the reaction, Isothermal Titration Calorimetry (ITC) was employed and the evolution of the hydrolysis products profile followed by HPLC, GPC and HPAEC-PAD. The ITC measurements revealed a second step, taking place at the end of the reaction, most probably resulting from disproportionation of accumulated fructo-oligosaccharides. As levanase, levansucrase may use levan as substrate and, through a fructosyl-enzyme complex, behave as a hydrolytic enzyme or as a transferase, as demonstrated when glucose and fructose are added as acceptors. These reactions result in a wide variety of oligosaccharides that are also suitable acceptors for fructo-oligosaccharide synthesis. Moreover, we demonstrate that SacB in the presence of levan and glucose, through blastose and sucrose synthesis, results in the same fructooligosaccharides profile as that observed in sucrose reactions. We conclude that SacB has an intrinsic levanase activity that contributes to the final levan profile in reactions with sucrose as substrate. |
format | Online Article Text |
id | pubmed-4658133 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-46581332015-12-02 Intrinsic Levanase Activity of Bacillus subtilis 168 Levansucrase (SacB) Méndez-Lorenzo, Luz Porras-Domínguez, Jaime R. Raga-Carbajal, Enrique Olvera, Clarita Rodríguez-Alegría, Maria Elena Carrillo-Nava, Ernesto Costas, Miguel López Munguía, Agustín PLoS One Research Article Levansucrase catalyzes the synthesis of fructose polymers through the transfer of fructosyl units from sucrose to a growing fructan chain. Levanase activity of Bacillus subtilis levansucrase has been described since the very first publications dealing with the mechanism of levan synthesis. However, there is a lack of qualitative and quantitative evidence regarding the importance of the intrinsic levan hydrolysis of B. subtilis levansucrase and its role in the levan synthesis process. Particularly, little attention has been paid to the long-term hydrolysis products, including its participation in the final levan molecules distribution. Here, we explored the hydrolytic and transferase activity of the B. subtilis levansucrase (SacB) when levans produced by the same enzyme are used as substrate. We found that levan is hydrolyzed through a first order exo-type mechanism, which is limited to a conversion extent of around 30% when all polymer molecules reach a structure no longer suitable to SacB hydrolysis. To characterize the reaction, Isothermal Titration Calorimetry (ITC) was employed and the evolution of the hydrolysis products profile followed by HPLC, GPC and HPAEC-PAD. The ITC measurements revealed a second step, taking place at the end of the reaction, most probably resulting from disproportionation of accumulated fructo-oligosaccharides. As levanase, levansucrase may use levan as substrate and, through a fructosyl-enzyme complex, behave as a hydrolytic enzyme or as a transferase, as demonstrated when glucose and fructose are added as acceptors. These reactions result in a wide variety of oligosaccharides that are also suitable acceptors for fructo-oligosaccharide synthesis. Moreover, we demonstrate that SacB in the presence of levan and glucose, through blastose and sucrose synthesis, results in the same fructooligosaccharides profile as that observed in sucrose reactions. We conclude that SacB has an intrinsic levanase activity that contributes to the final levan profile in reactions with sucrose as substrate. Public Library of Science 2015-11-23 /pmc/articles/PMC4658133/ /pubmed/26600431 http://dx.doi.org/10.1371/journal.pone.0143394 Text en © 2015 Méndez-Lorenzo 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 Méndez-Lorenzo, Luz Porras-Domínguez, Jaime R. Raga-Carbajal, Enrique Olvera, Clarita Rodríguez-Alegría, Maria Elena Carrillo-Nava, Ernesto Costas, Miguel López Munguía, Agustín Intrinsic Levanase Activity of Bacillus subtilis 168 Levansucrase (SacB) |
title | Intrinsic Levanase Activity of Bacillus subtilis 168 Levansucrase (SacB) |
title_full | Intrinsic Levanase Activity of Bacillus subtilis 168 Levansucrase (SacB) |
title_fullStr | Intrinsic Levanase Activity of Bacillus subtilis 168 Levansucrase (SacB) |
title_full_unstemmed | Intrinsic Levanase Activity of Bacillus subtilis 168 Levansucrase (SacB) |
title_short | Intrinsic Levanase Activity of Bacillus subtilis 168 Levansucrase (SacB) |
title_sort | intrinsic levanase activity of bacillus subtilis 168 levansucrase (sacb) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4658133/ https://www.ncbi.nlm.nih.gov/pubmed/26600431 http://dx.doi.org/10.1371/journal.pone.0143394 |
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