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High-efficiency expression and secretion of human FGF21 in Bacillus subtilis by intercalation of a mini-cistron cassette and combinatorial optimization of cell regulatory components
- Source :
- Microbial Cell Factories, Microbial Cell Factories, Vol 18, Iss 1, Pp 1-15 (2019)
- Publication Year :
- 2019
- Publisher :
- Springer Science and Business Media LLC, 2019.
-
Abstract
- Background Recombinant human Fibroblast growth factor 21 (rhFGF21) is an endocrine hormone that has profound effects on treatment of metabolic diseases. However, rhFGF21 is prone to form inclusion body when expressed in bacteria, which results in, the downstream process of purification of bioactive rhFGF21 is time-consuming and labor intensive. The aim of this work is to explore a new method for improving the soluble expression and secretion level of rhFGF21 in B. subtilis. Results A codon optimized rhFGF21 gene was expressed under the control of a strong inducible promoter PmalA in B. subtilis. A mini-cistron cassette (from gsiB) was located upstream of rhFGF21 in expression vector (pMATEFc5), which could reduce the locally stabilized mRNA secondary structure of transcripts and enhance the efficiency of translation initiation. Then various chaperones were further overexpressed to improve the expression efficiency of rhFGF21. Results showed that overexpression of the chaperone DnaK contributed to the increase of solubility of rhFGF21. Moreover, an extracellular proteases deficient strain B. subtilis Kno6cf was used to accumulate the secreted rhFGF21 solidly. In addition, eleven signal peptides from B. subtilis were evaluated and the SPdacB appeared the highest secretion yield of rhFGF21 in B. subtilis. Finally, the combinatorial optimized strain achieved an about ninefold increase of the soluble rhFGF21 production after 24 h of flask fermentation in comparison with the initial production strain. Conclusion This work provided a comprehensive strategy for secretory expressing the heterologous protein rhFGF21 in B. subtilis. To our knowledge, this is the first report of the highly efficient production of rhFGF21 in B. subtilis and this approach may provide some suggestions for heterologous proteins production in B. subtilis. Electronic supplementary material The online version of this article (10.1186/s12934-019-1066-4) contains supplementary material, which is available to authorized users.
- Subjects :
- Signal peptide
0106 biological sciences
Proteases
lcsh:QR1-502
Heterologous
Bioengineering
Chaperone
Bacillus subtilis
Protein Sorting Signals
01 natural sciences
Applied Microbiology and Biotechnology
lcsh:Microbiology
Heterologous protein expression
03 medical and health sciences
FGF21
Cistron
010608 biotechnology
Humans
Mini-cistron
Secretion
Codon
Promoter Regions, Genetic
0303 health sciences
Expression vector
biology
030306 microbiology
Chemistry
Research
biology.organism_classification
Recombinant Proteins
Fibroblast Growth Factors
Biochemistry
Chaperone (protein)
Fermentation
biology.protein
Molecular Chaperones
Biotechnology
Subjects
Details
- ISSN :
- 14752859
- Volume :
- 18
- Database :
- OpenAIRE
- Journal :
- Microbial Cell Factories
- Accession number :
- edsair.doi.dedup.....8316db7ebc6f7e3a6edf3f8b436ec87e