Recombinant expression and coexpression of oyster defensin and proline-rich peptide in Komagataella phaffii

Proline-rich peptide (CgPrp) and defensin (CgDef), oyster (Crassostrea gigas)-originated antimicrobial peptides (AMPs), were produced by the recombinant technique in Komagataella phaffii GS115 cells. For this purpose, the nucleotide sequences encoding the CgPrp and CgDef peptides were synthesized by...

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Published in:Biotechnology and Applied Biochemistry
Main Authors: Buyukkiraz, Mine Erdem, Kesmen, Zülal
Format: Article in Journal/Newspaper
Language:English
Published: 2021
Subjects:
Online Access:https://doi.org/10.1002/bab.2262
https://avesis.erciyes.edu.tr/publication/details/76c19c16-dfe8-4001-8e82-80ebbcec46ee/oai
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spelling fterciyesuniv:76c19c16-dfe8-4001-8e82-80ebbcec46ee 2023-05-15T15:58:47+02:00 Recombinant expression and coexpression of oyster defensin and proline-rich peptide in Komagataella phaffii Buyukkiraz, Mine Erdem Kesmen, Zülal 2021-10-01T00:00:00Z https://doi.org/10.1002/bab.2262 https://avesis.erciyes.edu.tr/publication/details/76c19c16-dfe8-4001-8e82-80ebbcec46ee/oai eng eng 76c19c16-dfe8-4001-8e82-80ebbcec46ee doi:10.1002/bab.2262 https://avesis.erciyes.edu.tr/publication/details/76c19c16-dfe8-4001-8e82-80ebbcec46ee/oai info:eu-repo/semantics/closedAccess info:eu-repo/semantics/article 2021 fterciyesuniv https://doi.org/10.1002/bab.2262 2022-02-13T14:29:08Z Proline-rich peptide (CgPrp) and defensin (CgDef), oyster (Crassostrea gigas)-originated antimicrobial peptides (AMPs), were produced by the recombinant technique in Komagataella phaffii GS115 cells. For this purpose, the nucleotide sequences encoding the CgPrp and CgDef peptides were synthesized by the recursive PCR technique, and ligated in pPICZaA expression vector. Additionally, the expression cassettes of pPICZ alpha A-CgDef and pPICZ alpha A-CgPrp were combined using in vitro multimer ligation strategy to construct the coexpression vector pPICZaA-CgPrp-CgDef. The expression and coexpression vectors transformed into K. phaffii GS115 cells by electroporation. At the end of the 0.5% methanol-induced expression stage for 96 h, the recombinant peptides were purified from the culture medium. The concentrations of purified peptides were changed between 1.05 and 1.21 mg/L. The recombinant peptides successfully inhibited the growth of tested Gram-positive bacterial strains belonging to Staphylococcus aureus, methicillin-resistant S. aureus (MRSA), Listeria monocytogenes, and Bacillus cereus. The minimum inhibitory concentrations (MIC) of recombinant CgPrp, CgDef, and CgPrp-CgDef peptides against tested bacteria were in the range of 12.50-25.00, 18.75-75.00, and 5.80-11.60 pg/mu l, respectively. The results of the study proved that the recombinant CgPrp, CgDef, and CgPrp-CgDef peptides expressed in K. phaffii might have good potential for the inhibition of common Gram-positive pathogenic bacteria, including drug-resistant MRSA. Article in Journal/Newspaper Crassostrea gigas Erciyes University Research Information System Biotechnology and Applied Biochemistry
institution Open Polar
collection Erciyes University Research Information System
op_collection_id fterciyesuniv
language English
description Proline-rich peptide (CgPrp) and defensin (CgDef), oyster (Crassostrea gigas)-originated antimicrobial peptides (AMPs), were produced by the recombinant technique in Komagataella phaffii GS115 cells. For this purpose, the nucleotide sequences encoding the CgPrp and CgDef peptides were synthesized by the recursive PCR technique, and ligated in pPICZaA expression vector. Additionally, the expression cassettes of pPICZ alpha A-CgDef and pPICZ alpha A-CgPrp were combined using in vitro multimer ligation strategy to construct the coexpression vector pPICZaA-CgPrp-CgDef. The expression and coexpression vectors transformed into K. phaffii GS115 cells by electroporation. At the end of the 0.5% methanol-induced expression stage for 96 h, the recombinant peptides were purified from the culture medium. The concentrations of purified peptides were changed between 1.05 and 1.21 mg/L. The recombinant peptides successfully inhibited the growth of tested Gram-positive bacterial strains belonging to Staphylococcus aureus, methicillin-resistant S. aureus (MRSA), Listeria monocytogenes, and Bacillus cereus. The minimum inhibitory concentrations (MIC) of recombinant CgPrp, CgDef, and CgPrp-CgDef peptides against tested bacteria were in the range of 12.50-25.00, 18.75-75.00, and 5.80-11.60 pg/mu l, respectively. The results of the study proved that the recombinant CgPrp, CgDef, and CgPrp-CgDef peptides expressed in K. phaffii might have good potential for the inhibition of common Gram-positive pathogenic bacteria, including drug-resistant MRSA.
format Article in Journal/Newspaper
author Buyukkiraz, Mine Erdem
Kesmen, Zülal
spellingShingle Buyukkiraz, Mine Erdem
Kesmen, Zülal
Recombinant expression and coexpression of oyster defensin and proline-rich peptide in Komagataella phaffii
author_facet Buyukkiraz, Mine Erdem
Kesmen, Zülal
author_sort Buyukkiraz, Mine Erdem
title Recombinant expression and coexpression of oyster defensin and proline-rich peptide in Komagataella phaffii
title_short Recombinant expression and coexpression of oyster defensin and proline-rich peptide in Komagataella phaffii
title_full Recombinant expression and coexpression of oyster defensin and proline-rich peptide in Komagataella phaffii
title_fullStr Recombinant expression and coexpression of oyster defensin and proline-rich peptide in Komagataella phaffii
title_full_unstemmed Recombinant expression and coexpression of oyster defensin and proline-rich peptide in Komagataella phaffii
title_sort recombinant expression and coexpression of oyster defensin and proline-rich peptide in komagataella phaffii
publishDate 2021
url https://doi.org/10.1002/bab.2262
https://avesis.erciyes.edu.tr/publication/details/76c19c16-dfe8-4001-8e82-80ebbcec46ee/oai
genre Crassostrea gigas
genre_facet Crassostrea gigas
op_relation 76c19c16-dfe8-4001-8e82-80ebbcec46ee
doi:10.1002/bab.2262
https://avesis.erciyes.edu.tr/publication/details/76c19c16-dfe8-4001-8e82-80ebbcec46ee/oai
op_rights info:eu-repo/semantics/closedAccess
op_doi https://doi.org/10.1002/bab.2262
container_title Biotechnology and Applied Biochemistry
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