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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...

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Autores principales: Knapp, Andreas, Voget, Sonja, Gao, Rong, Zaburannyi, Nestor, Krysciak, Dagmar, Breuer, Michael, Hauer, Bernhard, Streit, Wolfgang R., Müller, Rolf, Daniel, Rolf, Jaeger, Karl-Erich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2015
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.
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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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