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A Novel Hyaluronidase Produced by Bacillus sp. A50
Hyaluronidases are a family of enzymes that degrade hyaluronic acid (hyaluronan, HA) and widely used in many fields. A hyaluronidase producing bacteria strain was screened from the air. 16S ribosomal DNA (16S rDNA) analysis indicated that the strain belonged to the genus Bacillus, and the strain was...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3988017/ https://www.ncbi.nlm.nih.gov/pubmed/24736576 http://dx.doi.org/10.1371/journal.pone.0094156 |
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author | Guo, Xueping Shi, Yanli Sheng, Juzheng Wang, Fengshan |
author_facet | Guo, Xueping Shi, Yanli Sheng, Juzheng Wang, Fengshan |
author_sort | Guo, Xueping |
collection | PubMed |
description | Hyaluronidases are a family of enzymes that degrade hyaluronic acid (hyaluronan, HA) and widely used in many fields. A hyaluronidase producing bacteria strain was screened from the air. 16S ribosomal DNA (16S rDNA) analysis indicated that the strain belonged to the genus Bacillus, and the strain was named as Bacillus sp. A50. This is the first report of a hyaluronidase from Bacillus, which yields unsaturated oligosaccharides as product like other microbial hyaluronate lyases. Under optimized conditions, the yield of hyaluronidase from Bacillus sp. A50 could reach up to 1.5×10(4 )U/mL, suggesting that strain A50 is a good producer of hyaluronidase. The hyaluronidase (HAase-B) was isolated and purified from the bacterial culture, with a specific activity of 1.02×10(6) U/mg protein and a yield of 25.38%. The optimal temperature and pH of HAase-B were 44°C and pH 6.5, respectively. It was stable at pH 5–6 and at a temperature lower than 45°C. The enzymatic activity could be enhanced by Ca(2+), Mg(2+), or Ni(2+), and inhibited by Zn(2+), Cu(2+), EDTA, ethylene glycol tetraacetic acid (EGTA), deferoxamine mesylate salt (DFO), triton X-100, Tween 80, or SDS at different levels. Kinetic measurements of HAase-B towards HA gave a Michaelis constant (K (m)) of 0.02 mg/mL, and a maximum velocity (V (max)) of 0.27 A (232)/min. HAase-B also showed activity towards chondroitin sulfate A (CSA) with the kinetic parameters, K (m) and V (max), 12.30 mg/mL and 0.20 A (232)/min respectively. Meanwhile, according to the sequences of genomic DNA and HAase-B’s part peptides, a 3,324-bp gene encoding HAase-B was obtained. |
format | Online Article Text |
id | pubmed-3988017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39880172014-04-21 A Novel Hyaluronidase Produced by Bacillus sp. A50 Guo, Xueping Shi, Yanli Sheng, Juzheng Wang, Fengshan PLoS One Research Article Hyaluronidases are a family of enzymes that degrade hyaluronic acid (hyaluronan, HA) and widely used in many fields. A hyaluronidase producing bacteria strain was screened from the air. 16S ribosomal DNA (16S rDNA) analysis indicated that the strain belonged to the genus Bacillus, and the strain was named as Bacillus sp. A50. This is the first report of a hyaluronidase from Bacillus, which yields unsaturated oligosaccharides as product like other microbial hyaluronate lyases. Under optimized conditions, the yield of hyaluronidase from Bacillus sp. A50 could reach up to 1.5×10(4 )U/mL, suggesting that strain A50 is a good producer of hyaluronidase. The hyaluronidase (HAase-B) was isolated and purified from the bacterial culture, with a specific activity of 1.02×10(6) U/mg protein and a yield of 25.38%. The optimal temperature and pH of HAase-B were 44°C and pH 6.5, respectively. It was stable at pH 5–6 and at a temperature lower than 45°C. The enzymatic activity could be enhanced by Ca(2+), Mg(2+), or Ni(2+), and inhibited by Zn(2+), Cu(2+), EDTA, ethylene glycol tetraacetic acid (EGTA), deferoxamine mesylate salt (DFO), triton X-100, Tween 80, or SDS at different levels. Kinetic measurements of HAase-B towards HA gave a Michaelis constant (K (m)) of 0.02 mg/mL, and a maximum velocity (V (max)) of 0.27 A (232)/min. HAase-B also showed activity towards chondroitin sulfate A (CSA) with the kinetic parameters, K (m) and V (max), 12.30 mg/mL and 0.20 A (232)/min respectively. Meanwhile, according to the sequences of genomic DNA and HAase-B’s part peptides, a 3,324-bp gene encoding HAase-B was obtained. Public Library of Science 2014-04-15 /pmc/articles/PMC3988017/ /pubmed/24736576 http://dx.doi.org/10.1371/journal.pone.0094156 Text en © 2014 Guo 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 Guo, Xueping Shi, Yanli Sheng, Juzheng Wang, Fengshan A Novel Hyaluronidase Produced by Bacillus sp. A50 |
title | A Novel Hyaluronidase Produced by Bacillus sp. A50 |
title_full | A Novel Hyaluronidase Produced by Bacillus sp. A50 |
title_fullStr | A Novel Hyaluronidase Produced by Bacillus sp. A50 |
title_full_unstemmed | A Novel Hyaluronidase Produced by Bacillus sp. A50 |
title_short | A Novel Hyaluronidase Produced by Bacillus sp. A50 |
title_sort | novel hyaluronidase produced by bacillus sp. a50 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3988017/ https://www.ncbi.nlm.nih.gov/pubmed/24736576 http://dx.doi.org/10.1371/journal.pone.0094156 |
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