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Anchoring of heterologous proteins in multiple Lactobacillus species using anchors derived from Lactobacillus plantarum

Members of the genus Lactobacillus have a long history in food applications and are considered as promising and safe hosts for delivery of medically interesting proteins. We have assessed multiple surface anchors derived from Lactobacillus plantarum for protein surface display in multiple Lactobacil...

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Autores principales: Mathiesen, Geir, Øverland, Lise, Kuczkowska, Katarzyna, Eijsink, Vincent G. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7295990/
https://www.ncbi.nlm.nih.gov/pubmed/32541679
http://dx.doi.org/10.1038/s41598-020-66531-7
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author Mathiesen, Geir
Øverland, Lise
Kuczkowska, Katarzyna
Eijsink, Vincent G. H.
author_facet Mathiesen, Geir
Øverland, Lise
Kuczkowska, Katarzyna
Eijsink, Vincent G. H.
author_sort Mathiesen, Geir
collection PubMed
description Members of the genus Lactobacillus have a long history in food applications and are considered as promising and safe hosts for delivery of medically interesting proteins. We have assessed multiple surface anchors derived from Lactobacillus plantarum for protein surface display in multiple Lactobacillus species, using a Mycobacterium tuberculosis hybrid antigen as test protein. The anchors tested were a lipoprotein anchor and two cell wall anchors, one non-covalent (LysM domain) and one covalent (sortase-based anchoring using the LPXTG motif). Thus, three different expression vectors for surface-anchoring were tested in eight Lactobacillus species. When using the LPXTG and LysM cell wall anchors, surface display, as assessed by flow cytometry and fluorescence microscopy, was observed in all species except Lactobacillus acidophilus. Use of the cell membrane anchor revealed more variation in the apparent degree of surface-exposure among the various lactobacilli. Overproduction of the secreted and anchored antigen impaired bacterial growth rate to extents that varied among the lactobacilli and were dependent on the type of anchor. Overall, these results show that surface anchors derived from L. plantarum are promising candidates for efficient anchoring of medically interesting proteins in other food grade Lactobacillus species.
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spelling pubmed-72959902020-06-17 Anchoring of heterologous proteins in multiple Lactobacillus species using anchors derived from Lactobacillus plantarum Mathiesen, Geir Øverland, Lise Kuczkowska, Katarzyna Eijsink, Vincent G. H. Sci Rep Article Members of the genus Lactobacillus have a long history in food applications and are considered as promising and safe hosts for delivery of medically interesting proteins. We have assessed multiple surface anchors derived from Lactobacillus plantarum for protein surface display in multiple Lactobacillus species, using a Mycobacterium tuberculosis hybrid antigen as test protein. The anchors tested were a lipoprotein anchor and two cell wall anchors, one non-covalent (LysM domain) and one covalent (sortase-based anchoring using the LPXTG motif). Thus, three different expression vectors for surface-anchoring were tested in eight Lactobacillus species. When using the LPXTG and LysM cell wall anchors, surface display, as assessed by flow cytometry and fluorescence microscopy, was observed in all species except Lactobacillus acidophilus. Use of the cell membrane anchor revealed more variation in the apparent degree of surface-exposure among the various lactobacilli. Overproduction of the secreted and anchored antigen impaired bacterial growth rate to extents that varied among the lactobacilli and were dependent on the type of anchor. Overall, these results show that surface anchors derived from L. plantarum are promising candidates for efficient anchoring of medically interesting proteins in other food grade Lactobacillus species. Nature Publishing Group UK 2020-06-15 /pmc/articles/PMC7295990/ /pubmed/32541679 http://dx.doi.org/10.1038/s41598-020-66531-7 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Mathiesen, Geir
Øverland, Lise
Kuczkowska, Katarzyna
Eijsink, Vincent G. H.
Anchoring of heterologous proteins in multiple Lactobacillus species using anchors derived from Lactobacillus plantarum
title Anchoring of heterologous proteins in multiple Lactobacillus species using anchors derived from Lactobacillus plantarum
title_full Anchoring of heterologous proteins in multiple Lactobacillus species using anchors derived from Lactobacillus plantarum
title_fullStr Anchoring of heterologous proteins in multiple Lactobacillus species using anchors derived from Lactobacillus plantarum
title_full_unstemmed Anchoring of heterologous proteins in multiple Lactobacillus species using anchors derived from Lactobacillus plantarum
title_short Anchoring of heterologous proteins in multiple Lactobacillus species using anchors derived from Lactobacillus plantarum
title_sort anchoring of heterologous proteins in multiple lactobacillus species using anchors derived from lactobacillus plantarum
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7295990/
https://www.ncbi.nlm.nih.gov/pubmed/32541679
http://dx.doi.org/10.1038/s41598-020-66531-7
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