Cargando…
A novel trehalosamine isolated from Bacillus amyloliquefaciens and its antibacterial activities
Bacillus amyloliquefaciens has been widely used as a probiotic in the field of biological control,and its antibacterial compounds plays an important role in the prevention and control of plant, livestock and poultry diseases. It has the advantages of green, safe and efficiency. This study aims to se...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6960277/ https://www.ncbi.nlm.nih.gov/pubmed/31938970 http://dx.doi.org/10.1186/s13568-019-0943-x |
_version_ | 1783487759282864128 |
---|---|
author | Wang, Ying Zhao, Bo Liu, Yaping Mao, Linjing Zhang, Xuanming Meng, Wu Liu, Kechun Chu, Jie |
author_facet | Wang, Ying Zhao, Bo Liu, Yaping Mao, Linjing Zhang, Xuanming Meng, Wu Liu, Kechun Chu, Jie |
author_sort | Wang, Ying |
collection | PubMed |
description | Bacillus amyloliquefaciens has been widely used as a probiotic in the field of biological control,and its antibacterial compounds plays an important role in the prevention and control of plant, livestock and poultry diseases. It has the advantages of green, safe and efficiency. This study aims to separate and purify active ingredient from Bacillus amyloliquefaciens GN59 and study its antibacterial activity. A novel compound was isolated from GN59 by column chromatography on silica gel and HPLC purification. The chemical structure was identified as α-d-glucopyranosyl-(1 → 1′)-3′-amino-3′-deoxy-β-d-glucopyranoside (a,β-3-trehalosamine) on the basis of spectroscopic analysis. This is the first report about a,β-3-trehalosamine isolated from biological resources on an antibiotic activity against pathogenic bacterium. The 3′-neotrehalosamine displayed antibacterial activity across a broad spectrum of microorganisms, including different gram-positive and gram-negative bacteria, with minimal inhibitory concentration (MIC) values ranging from 0.5 to 0.7 mg/mL. The results indicated that the 3′-neotrehalosamine from GN59 might be a potential candidate for bactericide. |
format | Online Article Text |
id | pubmed-6960277 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-69602772020-01-30 A novel trehalosamine isolated from Bacillus amyloliquefaciens and its antibacterial activities Wang, Ying Zhao, Bo Liu, Yaping Mao, Linjing Zhang, Xuanming Meng, Wu Liu, Kechun Chu, Jie AMB Express Original Article Bacillus amyloliquefaciens has been widely used as a probiotic in the field of biological control,and its antibacterial compounds plays an important role in the prevention and control of plant, livestock and poultry diseases. It has the advantages of green, safe and efficiency. This study aims to separate and purify active ingredient from Bacillus amyloliquefaciens GN59 and study its antibacterial activity. A novel compound was isolated from GN59 by column chromatography on silica gel and HPLC purification. The chemical structure was identified as α-d-glucopyranosyl-(1 → 1′)-3′-amino-3′-deoxy-β-d-glucopyranoside (a,β-3-trehalosamine) on the basis of spectroscopic analysis. This is the first report about a,β-3-trehalosamine isolated from biological resources on an antibiotic activity against pathogenic bacterium. The 3′-neotrehalosamine displayed antibacterial activity across a broad spectrum of microorganisms, including different gram-positive and gram-negative bacteria, with minimal inhibitory concentration (MIC) values ranging from 0.5 to 0.7 mg/mL. The results indicated that the 3′-neotrehalosamine from GN59 might be a potential candidate for bactericide. Springer Berlin Heidelberg 2020-01-14 /pmc/articles/PMC6960277/ /pubmed/31938970 http://dx.doi.org/10.1186/s13568-019-0943-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Original Article Wang, Ying Zhao, Bo Liu, Yaping Mao, Linjing Zhang, Xuanming Meng, Wu Liu, Kechun Chu, Jie A novel trehalosamine isolated from Bacillus amyloliquefaciens and its antibacterial activities |
title | A novel trehalosamine isolated from Bacillus amyloliquefaciens and its antibacterial activities |
title_full | A novel trehalosamine isolated from Bacillus amyloliquefaciens and its antibacterial activities |
title_fullStr | A novel trehalosamine isolated from Bacillus amyloliquefaciens and its antibacterial activities |
title_full_unstemmed | A novel trehalosamine isolated from Bacillus amyloliquefaciens and its antibacterial activities |
title_short | A novel trehalosamine isolated from Bacillus amyloliquefaciens and its antibacterial activities |
title_sort | novel trehalosamine isolated from bacillus amyloliquefaciens and its antibacterial activities |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6960277/ https://www.ncbi.nlm.nih.gov/pubmed/31938970 http://dx.doi.org/10.1186/s13568-019-0943-x |
work_keys_str_mv | AT wangying anoveltrehalosamineisolatedfrombacillusamyloliquefaciensanditsantibacterialactivities AT zhaobo anoveltrehalosamineisolatedfrombacillusamyloliquefaciensanditsantibacterialactivities AT liuyaping anoveltrehalosamineisolatedfrombacillusamyloliquefaciensanditsantibacterialactivities AT maolinjing anoveltrehalosamineisolatedfrombacillusamyloliquefaciensanditsantibacterialactivities AT zhangxuanming anoveltrehalosamineisolatedfrombacillusamyloliquefaciensanditsantibacterialactivities AT mengwu anoveltrehalosamineisolatedfrombacillusamyloliquefaciensanditsantibacterialactivities AT liukechun anoveltrehalosamineisolatedfrombacillusamyloliquefaciensanditsantibacterialactivities AT chujie anoveltrehalosamineisolatedfrombacillusamyloliquefaciensanditsantibacterialactivities AT wangying noveltrehalosamineisolatedfrombacillusamyloliquefaciensanditsantibacterialactivities AT zhaobo noveltrehalosamineisolatedfrombacillusamyloliquefaciensanditsantibacterialactivities AT liuyaping noveltrehalosamineisolatedfrombacillusamyloliquefaciensanditsantibacterialactivities AT maolinjing noveltrehalosamineisolatedfrombacillusamyloliquefaciensanditsantibacterialactivities AT zhangxuanming noveltrehalosamineisolatedfrombacillusamyloliquefaciensanditsantibacterialactivities AT mengwu noveltrehalosamineisolatedfrombacillusamyloliquefaciensanditsantibacterialactivities AT liukechun noveltrehalosamineisolatedfrombacillusamyloliquefaciensanditsantibacterialactivities AT chujie noveltrehalosamineisolatedfrombacillusamyloliquefaciensanditsantibacterialactivities |