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Homogeneity and heterogeneity in amylase production by Bacillus subtilis under different growth conditions

BACKGROUND: Bacillus subtilis is an important cell factory for the biotechnological industry due to its ability to secrete commercially relevant proteins in large amounts directly into the growth medium. However, hyper-secretion of proteins, such as α-amylases, leads to induction of the secretion st...

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Autores principales: Ploss, Tina N., Reilman, Ewoud, Monteferrante, Carmine G., Denham, Emma L., Piersma, Sjouke, Lingner, Anja, Vehmaanperä, Jari, Lorenz, Patrick, van Dijl, Jan Maarten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4812647/
https://www.ncbi.nlm.nih.gov/pubmed/27026185
http://dx.doi.org/10.1186/s12934-016-0455-1
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author Ploss, Tina N.
Reilman, Ewoud
Monteferrante, Carmine G.
Denham, Emma L.
Piersma, Sjouke
Lingner, Anja
Vehmaanperä, Jari
Lorenz, Patrick
van Dijl, Jan Maarten
author_facet Ploss, Tina N.
Reilman, Ewoud
Monteferrante, Carmine G.
Denham, Emma L.
Piersma, Sjouke
Lingner, Anja
Vehmaanperä, Jari
Lorenz, Patrick
van Dijl, Jan Maarten
author_sort Ploss, Tina N.
collection PubMed
description BACKGROUND: Bacillus subtilis is an important cell factory for the biotechnological industry due to its ability to secrete commercially relevant proteins in large amounts directly into the growth medium. However, hyper-secretion of proteins, such as α-amylases, leads to induction of the secretion stress-responsive CssR-CssS regulatory system, resulting in up-regulation of the HtrA and HtrB proteases. These proteases degrade misfolded proteins secreted via the Sec pathway, resulting in a loss of product. The aim of this study was to investigate the secretion stress response in B. subtilis 168 cells overproducing the industrially relevant α-amylase AmyM from Geobacillus stearothermophilus, which was expressed from the strong promoter P(amyQ)-M. RESULTS: Here we show that activity of the htrB promoter as induced by overproduction of AmyM was “noisy”, which is indicative for heterogeneous activation of the secretion stress pathway. Plasmids were constructed to allow real-time analysis of P(amyQ)-M promoter activity and AmyM production by, respectively, transcriptional and out-of-frame translationally coupled fusions with gfpmut3. Our results show the emergence of distinct sub-populations of high- and low-level AmyM-producing cells, reflecting heterogeneity in the activity of P(amyQ)-M. This most likely explains the heterogeneous secretion stress response. Importantly, more homogenous cell populations with regard to P(amyQ)-M activity were observed for the B. subtilis mutant strain 168degUhy32, and the wild-type strain 168 under optimized growth conditions. CONCLUSION: Expression heterogeneity of secretory proteins in B. subtilis can be suppressed by degU mutation and optimized growth conditions. Further, the out-of-frame translational fusion of a gene for a secreted target protein and gfp represents a versatile tool for real-time monitoring of protein production and opens novel avenues for Bacillus production strain improvement.
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spelling pubmed-48126472016-03-31 Homogeneity and heterogeneity in amylase production by Bacillus subtilis under different growth conditions Ploss, Tina N. Reilman, Ewoud Monteferrante, Carmine G. Denham, Emma L. Piersma, Sjouke Lingner, Anja Vehmaanperä, Jari Lorenz, Patrick van Dijl, Jan Maarten Microb Cell Fact Research BACKGROUND: Bacillus subtilis is an important cell factory for the biotechnological industry due to its ability to secrete commercially relevant proteins in large amounts directly into the growth medium. However, hyper-secretion of proteins, such as α-amylases, leads to induction of the secretion stress-responsive CssR-CssS regulatory system, resulting in up-regulation of the HtrA and HtrB proteases. These proteases degrade misfolded proteins secreted via the Sec pathway, resulting in a loss of product. The aim of this study was to investigate the secretion stress response in B. subtilis 168 cells overproducing the industrially relevant α-amylase AmyM from Geobacillus stearothermophilus, which was expressed from the strong promoter P(amyQ)-M. RESULTS: Here we show that activity of the htrB promoter as induced by overproduction of AmyM was “noisy”, which is indicative for heterogeneous activation of the secretion stress pathway. Plasmids were constructed to allow real-time analysis of P(amyQ)-M promoter activity and AmyM production by, respectively, transcriptional and out-of-frame translationally coupled fusions with gfpmut3. Our results show the emergence of distinct sub-populations of high- and low-level AmyM-producing cells, reflecting heterogeneity in the activity of P(amyQ)-M. This most likely explains the heterogeneous secretion stress response. Importantly, more homogenous cell populations with regard to P(amyQ)-M activity were observed for the B. subtilis mutant strain 168degUhy32, and the wild-type strain 168 under optimized growth conditions. CONCLUSION: Expression heterogeneity of secretory proteins in B. subtilis can be suppressed by degU mutation and optimized growth conditions. Further, the out-of-frame translational fusion of a gene for a secreted target protein and gfp represents a versatile tool for real-time monitoring of protein production and opens novel avenues for Bacillus production strain improvement. BioMed Central 2016-03-29 /pmc/articles/PMC4812647/ /pubmed/27026185 http://dx.doi.org/10.1186/s12934-016-0455-1 Text en © Ploss et al. 2016 Open AccessThis 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Ploss, Tina N.
Reilman, Ewoud
Monteferrante, Carmine G.
Denham, Emma L.
Piersma, Sjouke
Lingner, Anja
Vehmaanperä, Jari
Lorenz, Patrick
van Dijl, Jan Maarten
Homogeneity and heterogeneity in amylase production by Bacillus subtilis under different growth conditions
title Homogeneity and heterogeneity in amylase production by Bacillus subtilis under different growth conditions
title_full Homogeneity and heterogeneity in amylase production by Bacillus subtilis under different growth conditions
title_fullStr Homogeneity and heterogeneity in amylase production by Bacillus subtilis under different growth conditions
title_full_unstemmed Homogeneity and heterogeneity in amylase production by Bacillus subtilis under different growth conditions
title_short Homogeneity and heterogeneity in amylase production by Bacillus subtilis under different growth conditions
title_sort homogeneity and heterogeneity in amylase production by bacillus subtilis under different growth conditions
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4812647/
https://www.ncbi.nlm.nih.gov/pubmed/27026185
http://dx.doi.org/10.1186/s12934-016-0455-1
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