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Fe Nanoparticles Enhanced Surfactin Production in Bacillus amyloliquefaciens

[Image: see text] Surfactin, as one of the most powerful biosurfactants, can be widely applied in agriculture, food, and pharmaceutics. However, low biosynthesis efficiency is the major obstacle in its commercialization. Here, we used nanoparticles to increase the surfactin production in Bacillus am...

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Detalles Bibliográficos
Autores principales: Yang, Na, Wu, Qun, Xu, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114131/
https://www.ncbi.nlm.nih.gov/pubmed/32258866
http://dx.doi.org/10.1021/acsomega.9b03648
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author Yang, Na
Wu, Qun
Xu, Yan
author_facet Yang, Na
Wu, Qun
Xu, Yan
author_sort Yang, Na
collection PubMed
description [Image: see text] Surfactin, as one of the most powerful biosurfactants, can be widely applied in agriculture, food, and pharmaceutics. However, low biosynthesis efficiency is the major obstacle in its commercialization. Here, we used nanoparticles to increase the surfactin production in Bacillus amyloliquefaciens MT45 through enhancing the secretion (the key step of surfactin biosynthesis). The results showed that the surfactin titer increased from 4.93 to 7.15 g/L in the flask and from 5.94 to 9.18 g/L in a 7 L bioreactor by adding 5 g/L Fe nanoparticles. They were the highest titers in the reported wild-type strain. Our results indicated that Fe nanoparticles enhanced the expression of genes involved in the biosynthesis of surfactin. Moreover, Fe nanoparticles increased the permeability of cell membranes, resulting in a more efficient secretion of surfactin. This study provides an efficient strategy for increasing the biosynthesis of microbial metabolites and provides new insights into the nanoparticles’ impacts on microbes.
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spelling pubmed-71141312020-04-03 Fe Nanoparticles Enhanced Surfactin Production in Bacillus amyloliquefaciens Yang, Na Wu, Qun Xu, Yan ACS Omega [Image: see text] Surfactin, as one of the most powerful biosurfactants, can be widely applied in agriculture, food, and pharmaceutics. However, low biosynthesis efficiency is the major obstacle in its commercialization. Here, we used nanoparticles to increase the surfactin production in Bacillus amyloliquefaciens MT45 through enhancing the secretion (the key step of surfactin biosynthesis). The results showed that the surfactin titer increased from 4.93 to 7.15 g/L in the flask and from 5.94 to 9.18 g/L in a 7 L bioreactor by adding 5 g/L Fe nanoparticles. They were the highest titers in the reported wild-type strain. Our results indicated that Fe nanoparticles enhanced the expression of genes involved in the biosynthesis of surfactin. Moreover, Fe nanoparticles increased the permeability of cell membranes, resulting in a more efficient secretion of surfactin. This study provides an efficient strategy for increasing the biosynthesis of microbial metabolites and provides new insights into the nanoparticles’ impacts on microbes. American Chemical Society 2020-03-20 /pmc/articles/PMC7114131/ /pubmed/32258866 http://dx.doi.org/10.1021/acsomega.9b03648 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Yang, Na
Wu, Qun
Xu, Yan
Fe Nanoparticles Enhanced Surfactin Production in Bacillus amyloliquefaciens
title Fe Nanoparticles Enhanced Surfactin Production in Bacillus amyloliquefaciens
title_full Fe Nanoparticles Enhanced Surfactin Production in Bacillus amyloliquefaciens
title_fullStr Fe Nanoparticles Enhanced Surfactin Production in Bacillus amyloliquefaciens
title_full_unstemmed Fe Nanoparticles Enhanced Surfactin Production in Bacillus amyloliquefaciens
title_short Fe Nanoparticles Enhanced Surfactin Production in Bacillus amyloliquefaciens
title_sort fe nanoparticles enhanced surfactin production in bacillus amyloliquefaciens
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114131/
https://www.ncbi.nlm.nih.gov/pubmed/32258866
http://dx.doi.org/10.1021/acsomega.9b03648
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