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Lactococcus lactis provides an efficient platform for production of disulfide-rich recombinant proteins from Plasmodium falciparum
- Source :
- Microbial Cell Factories, Vol 17, Iss 1, Pp 1-13 (2018), Singh, S K, Tiendrebeogo, R W, Chourasia, B K, Kana, I H, Singh, S & Theisen, M 2018, ' Lactococcus lactis provides an efficient platform for production of disulfide-rich recombinant proteins from Plasmodium falciparum ', Microbial Cell Factories, vol. 17, 55 . https://doi.org/10.1186/s12934-018-0902-2, Microbial Cell Factories
- Publication Year :
- 2018
- Publisher :
- BMC, 2018.
-
Abstract
- Background The production of recombinant proteins with proper conformation, appropriate post-translational modifications in an easily scalable and cost-effective system is challenging. Lactococcus lactis has recently been identified as an efficient Gram positive cell factory for the production of recombinant protein. We and others have used this expression host for the production of selected malaria vaccine candidates. The safety of this production system has been confirmed in multiple clinical trials. Here we have explored L. lactis cell factories for the production of 31 representative Plasmodium falciparum antigens with varying sizes (ranging from 9 to 90 kDa) and varying degree of predicted structural complexities including eleven antigens with multiple predicted structural disulfide bonds, those which are considered difficult-to-produce proteins. Results Of the 31 recombinant constructs attempted in the L. lactis expression system, the initial expression efficiency was 55% with 17 out of 31 recombinant gene constructs producing high levels of secreted recombinant protein. The majority of the constructs which failed to produce a recombinant protein were found to consist of multiple intra-molecular disulfide-bonds. We found that these disulfide-rich constructs could be produced in high yields when genetically fused to an intrinsically disorder protein domain (GLURP-R0). By exploiting the distinct biophysical and structural properties of the intrinsically disordered protein region we developed a simple heat-based strategy for fast purification of the disulfide-rich protein domains in yields ranging from 1 to 40 mg/l. Conclusions A novel procedure for the production and purification of disulfide-rich recombinant proteins in L. lactis is described. Electronic supplementary material The online version of this article (10.1186/s12934-018-0902-2) contains supplementary material, which is available to authorized users.
- Subjects :
- 0301 basic medicine
Disulfide-rich protein
Cell
Protein domain
Plasmodium falciparum
Protozoan Proteins
lcsh:QR1-502
Gene Expression
Bioengineering
Applied Microbiology and Biotechnology
lcsh:Microbiology
law.invention
03 medical and health sciences
Antigen
law
medicine
Merozoite antigens
Disulfides
Gene
biology
Malaria vaccine
Chemistry
Research
Lactococcus lactis
biology.organism_classification
Recombinant Proteins
Malaria
030104 developmental biology
medicine.anatomical_structure
Biochemistry
Recombinant DNA
Biotechnology
Subjects
Details
- Language :
- English
- ISSN :
- 14752859
- Volume :
- 17
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Microbial Cell Factories
- Accession number :
- edsair.doi.dedup.....8b41abfd9ae555c1c761d5bb884c5e7b