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Mutations improving production and secretion of extracellular lipase by Burkholderia glumae PG1
Burkholderia glumae is a Gram-negative phytopathogenic bacterium known as the causative agent of rice panicle blight. Strain B. glumae PG1 is used for the production of a biotechnologically relevant lipase, which is secreted into the culture supernatant via a type II secretion pathway. We have compa...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4717159/ https://www.ncbi.nlm.nih.gov/pubmed/26476653 http://dx.doi.org/10.1007/s00253-015-7041-z |
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author | Knapp, Andreas Voget, Sonja Gao, Rong Zaburannyi, Nestor Krysciak, Dagmar Breuer, Michael Hauer, Bernhard Streit, Wolfgang R. Müller, Rolf Daniel, Rolf Jaeger, Karl-Erich |
author_facet | Knapp, Andreas Voget, Sonja Gao, Rong Zaburannyi, Nestor Krysciak, Dagmar Breuer, Michael Hauer, Bernhard Streit, Wolfgang R. Müller, Rolf Daniel, Rolf Jaeger, Karl-Erich |
author_sort | Knapp, Andreas |
collection | PubMed |
description | Burkholderia glumae is a Gram-negative phytopathogenic bacterium known as the causative agent of rice panicle blight. Strain B. glumae PG1 is used for the production of a biotechnologically relevant lipase, which is secreted into the culture supernatant via a type II secretion pathway. We have comparatively analyzed the genome sequences of B. glumae PG1 wild type and a lipase overproducing strain obtained by classical strain mutagenesis. Among a total number of 72 single nucleotide polymorphisms (SNPs) identified in the genome of the production strain, two were localized in front of the lipAB operon and were analyzed in detail. Both mutations contribute to a 100-fold overproduction of extracellular lipase in B. glumae PG1 by affecting transcription of the lipAB operon and efficiency of lipase secretion. We analyzed each of the two SNPs separately and observed a stronger influence of the promoter mutation than of the signal peptide modification but also a cumulative effect of both mutations. Furthermore, fusion of the mutated LipA signal peptide resulted in a 2-fold increase in secretion of the heterologous reporter alkaline phosphatase from Escherichia coli. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00253-015-7041-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4717159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-47171592016-01-25 Mutations improving production and secretion of extracellular lipase by Burkholderia glumae PG1 Knapp, Andreas Voget, Sonja Gao, Rong Zaburannyi, Nestor Krysciak, Dagmar Breuer, Michael Hauer, Bernhard Streit, Wolfgang R. Müller, Rolf Daniel, Rolf Jaeger, Karl-Erich Appl Microbiol Biotechnol Biotechnologically Relevant Enzymes and Proteins Burkholderia glumae is a Gram-negative phytopathogenic bacterium known as the causative agent of rice panicle blight. Strain B. glumae PG1 is used for the production of a biotechnologically relevant lipase, which is secreted into the culture supernatant via a type II secretion pathway. We have comparatively analyzed the genome sequences of B. glumae PG1 wild type and a lipase overproducing strain obtained by classical strain mutagenesis. Among a total number of 72 single nucleotide polymorphisms (SNPs) identified in the genome of the production strain, two were localized in front of the lipAB operon and were analyzed in detail. Both mutations contribute to a 100-fold overproduction of extracellular lipase in B. glumae PG1 by affecting transcription of the lipAB operon and efficiency of lipase secretion. We analyzed each of the two SNPs separately and observed a stronger influence of the promoter mutation than of the signal peptide modification but also a cumulative effect of both mutations. Furthermore, fusion of the mutated LipA signal peptide resulted in a 2-fold increase in secretion of the heterologous reporter alkaline phosphatase from Escherichia coli. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00253-015-7041-z) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2015-10-17 2016 /pmc/articles/PMC4717159/ /pubmed/26476653 http://dx.doi.org/10.1007/s00253-015-7041-z Text en © The Author(s) 2015 Open Access This 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. |
spellingShingle | Biotechnologically Relevant Enzymes and Proteins Knapp, Andreas Voget, Sonja Gao, Rong Zaburannyi, Nestor Krysciak, Dagmar Breuer, Michael Hauer, Bernhard Streit, Wolfgang R. Müller, Rolf Daniel, Rolf Jaeger, Karl-Erich Mutations improving production and secretion of extracellular lipase by Burkholderia glumae PG1 |
title | Mutations improving production and secretion of extracellular lipase by Burkholderia glumae PG1 |
title_full | Mutations improving production and secretion of extracellular lipase by Burkholderia glumae PG1 |
title_fullStr | Mutations improving production and secretion of extracellular lipase by Burkholderia glumae PG1 |
title_full_unstemmed | Mutations improving production and secretion of extracellular lipase by Burkholderia glumae PG1 |
title_short | Mutations improving production and secretion of extracellular lipase by Burkholderia glumae PG1 |
title_sort | mutations improving production and secretion of extracellular lipase by burkholderia glumae pg1 |
topic | Biotechnologically Relevant Enzymes and Proteins |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4717159/ https://www.ncbi.nlm.nih.gov/pubmed/26476653 http://dx.doi.org/10.1007/s00253-015-7041-z |
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