Heterologous protein secretion by bacillus species from the cradle to the grave
- PMID: 20800757
- DOI: 10.1016/S0065-2164(10)73001-X
Heterologous protein secretion by bacillus species from the cradle to the grave
Abstract
The Gram-positive bacterium Bacillus subtilis and some of its close relatives are widely used for the industrial production of enzymes for the detergents, food, and beverage industries. The choice of these organisms is based almost exclusively on the high capacity of their secretion systems that are, under the right conditions, able to secrete proteins at grams per liter concentrations. In contrast, there are relatively few examples of Bacillus species being used for the cytoplasmic production of proteins. The range of proteins that are capable of high-level production and secretion is limited by a combination of characteristics of both the target protein and the host bacterium. The secretion pathway includes checkpoints that are designed to validate the authenticity of pathway substrates. Although many of these checkpoints are known, only some can be overcome by reengineering the host. As a result, the yield of heterologous protein production is extremely variable. In this review, we consider the Bacillus protein secretion pathway from the synthesis of the target protein (cradle) to its emergence at the outer surface of the complex cell wall (grave), and discuss the roles of the various checkpoints both with respect to the target protein and their role on cell homeostasis.
Copyright © 2010 Elsevier Inc. All rights reserved.
Similar articles
-
Exploitation of Bacillus subtilis as a robust workhorse for production of heterologous proteins and beyond.World J Microbiol Biotechnol. 2018 Sep 10;34(10):145. doi: 10.1007/s11274-018-2531-7. World J Microbiol Biotechnol. 2018. PMID: 30203131 Review.
-
Recombinant production of the antibody fragment D1.3 scFv with different Bacillus strains.Microb Cell Fact. 2017 Jan 23;16(1):14. doi: 10.1186/s12934-017-0625-9. Microb Cell Fact. 2017. PMID: 28115011 Free PMC article.
-
Relative contributions of non-essential Sec pathway components and cell envelope-associated proteases to high-level enzyme secretion by Bacillus subtilis.Microb Cell Fact. 2020 Feb 28;19(1):52. doi: 10.1186/s12934-020-01315-2. Microb Cell Fact. 2020. PMID: 32111210 Free PMC article.
-
Comparative analysis of twin-arginine (Tat)-dependent protein secretion of a heterologous model protein (GFP) in three different Gram-positive bacteria.Appl Microbiol Biotechnol. 2007 Sep;76(3):633-42. doi: 10.1007/s00253-007-0934-8. Epub 2007 Apr 24. Appl Microbiol Biotechnol. 2007. PMID: 17453196
-
Bacillus subtilis as cell factory for pharmaceutical proteins: a biotechnological approach to optimize the host organism.Biochim Biophys Acta. 2004 Nov 11;1694(1-3):299-310. doi: 10.1016/j.bbamcr.2004.02.011. Biochim Biophys Acta. 2004. PMID: 15546673 Review.
Cited by
-
Stable expression plasmids for Streptomyces based on a toxin-antitoxin system.Microb Cell Fact. 2013 Apr 25;12:39. doi: 10.1186/1475-2859-12-39. Microb Cell Fact. 2013. PMID: 23617558 Free PMC article.
-
Genome engineering using a synthetic gene circuit in Bacillus subtilis.Nucleic Acids Res. 2015 Mar 31;43(6):e42. doi: 10.1093/nar/gku1380. Epub 2014 Dec 30. Nucleic Acids Res. 2015. PMID: 25552415 Free PMC article.
-
Growth of Bacillus amyloliquefaciens as influence by Si nutrition.Arch Microbiol. 2021 Sep;203(7):4329-4336. doi: 10.1007/s00203-021-02421-4. Epub 2021 Jun 10. Arch Microbiol. 2021. PMID: 34114085
-
Optimization of Signal Peptide via Site-Directed Mutagenesis for Enhanced Secretion of Heterologous Proteins in Lactococcus lactis.Int J Mol Sci. 2022 Sep 2;23(17):10044. doi: 10.3390/ijms231710044. Int J Mol Sci. 2022. PMID: 36077441 Free PMC article.
-
The ins and outs of Bacillus proteases: activities, functions and commercial significance.FEMS Microbiol Rev. 2022 Jan 18;46(1):fuab046. doi: 10.1093/femsre/fuab046. FEMS Microbiol Rev. 2022. PMID: 34410368 Free PMC article. Review.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials