Mutations improving production and secretion of extracellular lipase by Burkholderia glumae PG1

• Published in: Applied microbiology and biotechnology 2016-02, Vol.100 (3), p.1265-1273
• Main Authors: Knapp, Andreas, Voget, Sonja, Gao, Rong, Zaburannyi, Nestor, Krysciak, Dagmar, Breuer, Michael, Hauer, Bernhard, Streit, Wolfgang R, Müller, Rolf, Daniel, Rolf, Jaeger, Karl-Erich
• Format: Article
• Language: English
• Subjects: Agricultural biotechnology; alkaline phosphatase; Biomedical and Life Sciences; Biotechnologically Relevant Enzymes and Proteins; Biotechnology; blight; Burkholderia; Burkholderia glumae; E coli; Enzymes; Escherichia coli; Extracellular matrix; Gene mutation; Genetic aspects; Genomes; Health aspects; inflorescences; Life Sciences; Lipase; Lipids; Microbial Genetics and Genomics; Microbiology; Mutagenesis; Mutation; nucleotide sequences; Observations; operon; Pathogens; Peptides; Pharmaceuticals; Plant diseases; plant pathogenic bacteria; rice; secretion; signal peptide; single nucleotide polymorphism; Studies; Surfactants; transcription (genetics); type II secretion system
• ISSN: 0175-7598; 1432-0614
• DOI: 10.1007/s00253-015-7041-z

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.