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Genome-wide analysis of signal peptide functionality in Lactobacillus plantarum WCFS1

BACKGROUND: Lactobacillus plantarum is a normal, potentially probiotic, inhabitant of the human gastrointestinal (GI) tract. The bacterium has great potential as food-grade cell factory and for in situ delivery of biomolecules. Since protein secretion is important both for probiotic activity and in...

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Autores principales: Mathiesen, Geir, Sveen, Anita, Brurberg, May Bente, Fredriksen, Lasse, Axelsson, Lars, Eijsink, Vincent GH
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2748100/
https://www.ncbi.nlm.nih.gov/pubmed/19744343
http://dx.doi.org/10.1186/1471-2164-10-425
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author Mathiesen, Geir
Sveen, Anita
Brurberg, May Bente
Fredriksen, Lasse
Axelsson, Lars
Eijsink, Vincent GH
author_facet Mathiesen, Geir
Sveen, Anita
Brurberg, May Bente
Fredriksen, Lasse
Axelsson, Lars
Eijsink, Vincent GH
author_sort Mathiesen, Geir
collection PubMed
description BACKGROUND: Lactobacillus plantarum is a normal, potentially probiotic, inhabitant of the human gastrointestinal (GI) tract. The bacterium has great potential as food-grade cell factory and for in situ delivery of biomolecules. Since protein secretion is important both for probiotic activity and in biotechnological applications, we have carried out a genome-wide experimental study of signal peptide (SP) functionality. RESULTS: We have constructed a library of 76 Sec-type signal peptides from L. plantarum WCFS1 that were predicted to be cleaved by signal peptidase I. SP functionality was studied using staphylococcal nuclease (NucA) as a reporter protein. 82% of the SPs gave significant extracellular NucA activity. Levels of secreted NucA varied by a dramatic 1800-fold and this variation was shown not to be the result of different mRNA levels. For the best-performing SPs all produced NucA was detected in the culture supernatant, but the secretion efficiency decreased for the less well performing SPs. Sequence analyses of the SPs and their cognate proteins revealed four properties that correlated positively with SP performance for NucA: high hydrophobicity, the presence of a transmembrane helix predicted by TMHMM, the absence of an anchoring motif in the cognate protein, and the length of the H+C domain. Analysis of a subset of SPs with a lactobacillal amylase (AmyA) showed large variation in production levels and secretion efficiencies. Importantly, there was no correlation between SP performance with NucA and the performance with AmyA. CONCLUSION: This is the first comprehensive experimental study showing that predicted SPs in the L. plantarum genome actually are capable of driving protein secretion. The results reveal considerable variation between the SPs that is at least in part dependent on the protein that is secreted. Several SPs stand out as promising candidates for efficient secretion of heterologous proteins in L. plantarum. The results for NucA provide some hints as to the sequence-based prediction of SP functionality, but the general conclusion is that such prediction is difficult. The vector library generated in this study is based on exchangeable cassettes and provides a powerful tool for rapid experimental screening of SPs.
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spelling pubmed-27481002009-09-22 Genome-wide analysis of signal peptide functionality in Lactobacillus plantarum WCFS1 Mathiesen, Geir Sveen, Anita Brurberg, May Bente Fredriksen, Lasse Axelsson, Lars Eijsink, Vincent GH BMC Genomics Research Article BACKGROUND: Lactobacillus plantarum is a normal, potentially probiotic, inhabitant of the human gastrointestinal (GI) tract. The bacterium has great potential as food-grade cell factory and for in situ delivery of biomolecules. Since protein secretion is important both for probiotic activity and in biotechnological applications, we have carried out a genome-wide experimental study of signal peptide (SP) functionality. RESULTS: We have constructed a library of 76 Sec-type signal peptides from L. plantarum WCFS1 that were predicted to be cleaved by signal peptidase I. SP functionality was studied using staphylococcal nuclease (NucA) as a reporter protein. 82% of the SPs gave significant extracellular NucA activity. Levels of secreted NucA varied by a dramatic 1800-fold and this variation was shown not to be the result of different mRNA levels. For the best-performing SPs all produced NucA was detected in the culture supernatant, but the secretion efficiency decreased for the less well performing SPs. Sequence analyses of the SPs and their cognate proteins revealed four properties that correlated positively with SP performance for NucA: high hydrophobicity, the presence of a transmembrane helix predicted by TMHMM, the absence of an anchoring motif in the cognate protein, and the length of the H+C domain. Analysis of a subset of SPs with a lactobacillal amylase (AmyA) showed large variation in production levels and secretion efficiencies. Importantly, there was no correlation between SP performance with NucA and the performance with AmyA. CONCLUSION: This is the first comprehensive experimental study showing that predicted SPs in the L. plantarum genome actually are capable of driving protein secretion. The results reveal considerable variation between the SPs that is at least in part dependent on the protein that is secreted. Several SPs stand out as promising candidates for efficient secretion of heterologous proteins in L. plantarum. The results for NucA provide some hints as to the sequence-based prediction of SP functionality, but the general conclusion is that such prediction is difficult. The vector library generated in this study is based on exchangeable cassettes and provides a powerful tool for rapid experimental screening of SPs. BioMed Central 2009-09-10 /pmc/articles/PMC2748100/ /pubmed/19744343 http://dx.doi.org/10.1186/1471-2164-10-425 Text en Copyright © 2009 Mathiesen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Mathiesen, Geir
Sveen, Anita
Brurberg, May Bente
Fredriksen, Lasse
Axelsson, Lars
Eijsink, Vincent GH
Genome-wide analysis of signal peptide functionality in Lactobacillus plantarum WCFS1
title Genome-wide analysis of signal peptide functionality in Lactobacillus plantarum WCFS1
title_full Genome-wide analysis of signal peptide functionality in Lactobacillus plantarum WCFS1
title_fullStr Genome-wide analysis of signal peptide functionality in Lactobacillus plantarum WCFS1
title_full_unstemmed Genome-wide analysis of signal peptide functionality in Lactobacillus plantarum WCFS1
title_short Genome-wide analysis of signal peptide functionality in Lactobacillus plantarum WCFS1
title_sort genome-wide analysis of signal peptide functionality in lactobacillus plantarum wcfs1
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2748100/
https://www.ncbi.nlm.nih.gov/pubmed/19744343
http://dx.doi.org/10.1186/1471-2164-10-425
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