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Purification and characterization of α-Amylase from Miswak Salvadora persica

BACKGROUND: The miswak (Salvadora persica) is a natural toothbrush. It is well known that very little information has been reported on enzymes in miswak as medicinal plant. Recently, we study peroxidase in miswak. In the present study, the main goal of this work is to purify and characterize α-amyla...

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Autores principales: Mohamed, Saleh A, Almulaiky, Yaaser Q, Ahmed, Youssri M, Al-Bar, Omar AM, Ibrahim, Ibrahim H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974154/
https://www.ncbi.nlm.nih.gov/pubmed/24690287
http://dx.doi.org/10.1186/1472-6882-14-119
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author Mohamed, Saleh A
Almulaiky, Yaaser Q
Ahmed, Youssri M
Al-Bar, Omar AM
Ibrahim, Ibrahim H
author_facet Mohamed, Saleh A
Almulaiky, Yaaser Q
Ahmed, Youssri M
Al-Bar, Omar AM
Ibrahim, Ibrahim H
author_sort Mohamed, Saleh A
collection PubMed
description BACKGROUND: The miswak (Salvadora persica) is a natural toothbrush. It is well known that very little information has been reported on enzymes in miswak as medicinal plant. Recently, we study peroxidase in miswak. In the present study, the main goal of this work is to purify and characterize α-amylase from miswak. The second goal is to study the storage stability of α-amylase in toothpaste. METHOD: The purification method included chromatographaphy of miswak α-amylase on DEAE-Sepharose column and Sephacryl S-200 column. Molecular weight was determined by gel filtration and SDS-PAGE. RESULTS: Five α-amylases A1, A4a, A4b, A5a and A5b from miswak were purified and they had molecular weights of 14, 74, 16, 30 and 20 kDa, respectively. α-Amylases had optimum pH from 6 to 8. Affinity of the substrates toward all enzymes was studied. Miswak α-amylases A1, A4a, A4b, A5a and A5b had Km values for starch and glycogen of 3.7, 3.7, 7.1, 0.52, 4.3 mg/ml and 5.95, 5.9 4.16, 6.3, 6.49 mg/ml, respectively. The optimum temperature for five enzymes ranged 40°C- 60°C. Miswak α-amylases were stable up to 40°C- 60°C after incubation for 30 min. Ca(+2) activated all the miswak α-amylases, while Ni(2+), Co(+2) and Zn(+2) activated or inhibited some of these enzymes. The metal chelators, EDTA, sodium citrate and sodium oxalate had inhibitory effects on miswak α-amylases. PMSF, p-HMB, DTNB and 1,10 phenanthroline caused inhibitory effect on α-amylases. The analysis of hydrolytic products after starch hydrolysis by miswak α-amylases on paper chromatography revealed that glucose, maltose, maltotriose and oligosaccharide were the major products. Crude miswak α-amylase in the toothpaste retained 55% of its original activity after 10 months of storage at room temperature. CONCLUSIONS: From these findings, α-amylases from miswak can be considered as beneficial enzymes for pharmaceuticals. Therefore, we study the storage stability of the crude α-amylase of miswak, which contained the five α-amylases, in toothpaste. The enzyme in the toothpaste retained 55% of its original activity after 10 months of storage at room temperature.
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spelling pubmed-39741542014-04-04 Purification and characterization of α-Amylase from Miswak Salvadora persica Mohamed, Saleh A Almulaiky, Yaaser Q Ahmed, Youssri M Al-Bar, Omar AM Ibrahim, Ibrahim H BMC Complement Altern Med Research Article BACKGROUND: The miswak (Salvadora persica) is a natural toothbrush. It is well known that very little information has been reported on enzymes in miswak as medicinal plant. Recently, we study peroxidase in miswak. In the present study, the main goal of this work is to purify and characterize α-amylase from miswak. The second goal is to study the storage stability of α-amylase in toothpaste. METHOD: The purification method included chromatographaphy of miswak α-amylase on DEAE-Sepharose column and Sephacryl S-200 column. Molecular weight was determined by gel filtration and SDS-PAGE. RESULTS: Five α-amylases A1, A4a, A4b, A5a and A5b from miswak were purified and they had molecular weights of 14, 74, 16, 30 and 20 kDa, respectively. α-Amylases had optimum pH from 6 to 8. Affinity of the substrates toward all enzymes was studied. Miswak α-amylases A1, A4a, A4b, A5a and A5b had Km values for starch and glycogen of 3.7, 3.7, 7.1, 0.52, 4.3 mg/ml and 5.95, 5.9 4.16, 6.3, 6.49 mg/ml, respectively. The optimum temperature for five enzymes ranged 40°C- 60°C. Miswak α-amylases were stable up to 40°C- 60°C after incubation for 30 min. Ca(+2) activated all the miswak α-amylases, while Ni(2+), Co(+2) and Zn(+2) activated or inhibited some of these enzymes. The metal chelators, EDTA, sodium citrate and sodium oxalate had inhibitory effects on miswak α-amylases. PMSF, p-HMB, DTNB and 1,10 phenanthroline caused inhibitory effect on α-amylases. The analysis of hydrolytic products after starch hydrolysis by miswak α-amylases on paper chromatography revealed that glucose, maltose, maltotriose and oligosaccharide were the major products. Crude miswak α-amylase in the toothpaste retained 55% of its original activity after 10 months of storage at room temperature. CONCLUSIONS: From these findings, α-amylases from miswak can be considered as beneficial enzymes for pharmaceuticals. Therefore, we study the storage stability of the crude α-amylase of miswak, which contained the five α-amylases, in toothpaste. The enzyme in the toothpaste retained 55% of its original activity after 10 months of storage at room temperature. BioMed Central 2014-04-01 /pmc/articles/PMC3974154/ /pubmed/24690287 http://dx.doi.org/10.1186/1472-6882-14-119 Text en Copyright © 2014 Mohamed et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Mohamed, Saleh A
Almulaiky, Yaaser Q
Ahmed, Youssri M
Al-Bar, Omar AM
Ibrahim, Ibrahim H
Purification and characterization of α-Amylase from Miswak Salvadora persica
title Purification and characterization of α-Amylase from Miswak Salvadora persica
title_full Purification and characterization of α-Amylase from Miswak Salvadora persica
title_fullStr Purification and characterization of α-Amylase from Miswak Salvadora persica
title_full_unstemmed Purification and characterization of α-Amylase from Miswak Salvadora persica
title_short Purification and characterization of α-Amylase from Miswak Salvadora persica
title_sort purification and characterization of α-amylase from miswak salvadora persica
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974154/
https://www.ncbi.nlm.nih.gov/pubmed/24690287
http://dx.doi.org/10.1186/1472-6882-14-119
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