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Production of trehalose with trehalose synthase expressed and displayed on the surface of Bacillus subtilis spores
BACKGROUND: Bacillus subtilis spores have been commonly used for the surface display of various food-related or human antigens or enzymes. For successful display, the target protein needs to be fused with an anchor protein. The preferred anchored proteins are the outer-coat proteins of spores; outer...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6547511/ https://www.ncbi.nlm.nih.gov/pubmed/31159804 http://dx.doi.org/10.1186/s12934-019-1152-7 |
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author | Liu, Hongling Yang, Shaojie Wang, Xihui Wang, Tengfei |
author_facet | Liu, Hongling Yang, Shaojie Wang, Xihui Wang, Tengfei |
author_sort | Liu, Hongling |
collection | PubMed |
description | BACKGROUND: Bacillus subtilis spores have been commonly used for the surface display of various food-related or human antigens or enzymes. For successful display, the target protein needs to be fused with an anchor protein. The preferred anchored proteins are the outer-coat proteins of spores; outer-coat proteins G (CotG) and C (CotC) are commonly used. In this study, mutant trehalose synthase (V407M/K490L/R680E TreS) was displayed on the surface of B. subtilis WB800n spores using CotG and CotC individually or in combination as an anchoring protein. RESULTS: Western blotting, immunofluorescence, dot blot, and enzymatic-activity assays detected TreS on the spore surface. The TreS activity with CotC and CotG together as the anchor protein was greater than the sum of the enzymatic activities with CotC or CotG alone. The TreS displayed on the spore surface with CotC and CotG together as the anchoring protein showed elevated and stable specific activity. To ensure spore stability and prevent spore germination in the trehalose preparation system, two germination-specific lytic genes, sleB and cwlJ, were deleted from the B. subtilis WB800n genome. It was demonstrated that this deletion did not affect the growth and spore formation of B. subtilis WB800n but strongly inhibited germination of the spores during transformation. The conversion rate of trehalose from 300 g/L maltose by B. subtilis strain WB800n(ΔsleB, ΔcwlJ)/cotC-treS–cotG-treS was 74.1% at 12 h (350 U/[g maltose]), and its enzymatic activity was largely retained, with a conversion rate of 73% after four cycles. CONCLUSIONS: The spore surface display system based on food-grade B. subtilis with CotC and CotG as a combined carrier appears to be a powerful technology for TreS expression, which may be used for the biotransformation of d-maltose into d-trehalose. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12934-019-1152-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6547511 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65475112019-06-06 Production of trehalose with trehalose synthase expressed and displayed on the surface of Bacillus subtilis spores Liu, Hongling Yang, Shaojie Wang, Xihui Wang, Tengfei Microb Cell Fact Research BACKGROUND: Bacillus subtilis spores have been commonly used for the surface display of various food-related or human antigens or enzymes. For successful display, the target protein needs to be fused with an anchor protein. The preferred anchored proteins are the outer-coat proteins of spores; outer-coat proteins G (CotG) and C (CotC) are commonly used. In this study, mutant trehalose synthase (V407M/K490L/R680E TreS) was displayed on the surface of B. subtilis WB800n spores using CotG and CotC individually or in combination as an anchoring protein. RESULTS: Western blotting, immunofluorescence, dot blot, and enzymatic-activity assays detected TreS on the spore surface. The TreS activity with CotC and CotG together as the anchor protein was greater than the sum of the enzymatic activities with CotC or CotG alone. The TreS displayed on the spore surface with CotC and CotG together as the anchoring protein showed elevated and stable specific activity. To ensure spore stability and prevent spore germination in the trehalose preparation system, two germination-specific lytic genes, sleB and cwlJ, were deleted from the B. subtilis WB800n genome. It was demonstrated that this deletion did not affect the growth and spore formation of B. subtilis WB800n but strongly inhibited germination of the spores during transformation. The conversion rate of trehalose from 300 g/L maltose by B. subtilis strain WB800n(ΔsleB, ΔcwlJ)/cotC-treS–cotG-treS was 74.1% at 12 h (350 U/[g maltose]), and its enzymatic activity was largely retained, with a conversion rate of 73% after four cycles. CONCLUSIONS: The spore surface display system based on food-grade B. subtilis with CotC and CotG as a combined carrier appears to be a powerful technology for TreS expression, which may be used for the biotransformation of d-maltose into d-trehalose. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12934-019-1152-7) contains supplementary material, which is available to authorized users. BioMed Central 2019-06-03 /pmc/articles/PMC6547511/ /pubmed/31159804 http://dx.doi.org/10.1186/s12934-019-1152-7 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Liu, Hongling Yang, Shaojie Wang, Xihui Wang, Tengfei Production of trehalose with trehalose synthase expressed and displayed on the surface of Bacillus subtilis spores |
title | Production of trehalose with trehalose synthase expressed and displayed on the surface of Bacillus subtilis spores |
title_full | Production of trehalose with trehalose synthase expressed and displayed on the surface of Bacillus subtilis spores |
title_fullStr | Production of trehalose with trehalose synthase expressed and displayed on the surface of Bacillus subtilis spores |
title_full_unstemmed | Production of trehalose with trehalose synthase expressed and displayed on the surface of Bacillus subtilis spores |
title_short | Production of trehalose with trehalose synthase expressed and displayed on the surface of Bacillus subtilis spores |
title_sort | production of trehalose with trehalose synthase expressed and displayed on the surface of bacillus subtilis spores |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6547511/ https://www.ncbi.nlm.nih.gov/pubmed/31159804 http://dx.doi.org/10.1186/s12934-019-1152-7 |
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