Analysis of different signal peptides for the secretory production of Ama r 2 in gram-positive systems (Lactococcus lactis).


Journal

Microbial pathogenesis
ISSN: 1096-1208
Titre abrégé: Microb Pathog
Pays: England
ID NLM: 8606191

Informations de publication

Date de publication:
Jan 2020
Historique:
received: 04 09 2019
revised: 22 10 2019
accepted: 23 10 2019
pubmed: 2 11 2019
medline: 21 10 2020
entrez: 1 11 2019
Statut: ppublish

Résumé

Prokaryotic systems have been considered the most affordable and simplest hosts which are being employed to express recombinant proteins such as allergens; nevertheless, without appropriate signal peptide (SP), these systems cannot be used for secretory proteins. Recently, a lot of effort has been put into assessing the potential of gram-positive strains such as lactic acid bacteria for new applications in the production of heterologous proteins. Ama r 2 is a respiratory allergen from Amaranthus retroflexus, whose recombinant production in the probiotic host could be introduced as a specific and effective way to rapid diagnosis and immunotherapy of this allergy. Consequently, the production of this recombinant protein using the prokaryotic system, requires a suitable SP to protect disulfide bonds and to prevent misfolding. This study was designed to predict the best SPs for the expression of Ama r 2 protein in Lactococcus lactis as the host. In this study, 42 signal sequences were selected from SP databases and the most important features of them were evaluated. First, n, h and c regions of the SPs and their probabilities were investigated by signalP software version 4.1. Then, their physicochemical properties were evaluated by Portparam and SOLpro. Moreover, the secretion sorting and sub-cellular localization sites were evaluated by PRED-TAT and ProtcompB software programs. The results revealed that yjgB, entC2 (Entrotoxine type C-2), ent B (Entrotoxine type), blaZ (Beta lactamase), dex (number 21), blm (Beta lactamase 2), dex (Dextranase; number 20) and number 26 were introduced theatrically as the best SPs to express Ama r 2 in Lactococcus lactis.

Identifiants

pubmed: 31669829
pii: S0882-4010(19)31575-X
doi: 10.1016/j.micpath.2019.103819
pii:
doi:

Substances chimiques

Plant Proteins 0
Protein Sorting Signals 0
Recombinant Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

103819

Informations de copyright

Copyright © 2019. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare no conflict of interest, financial or otherwise.

Auteurs

Alireza Vasiee (A)

Department of Food Science and Technology, Faculty of Agriculture, Ferdowsi University of Mashhad, Mashhad, Iran.

Neda Norouzi (N)

University Medical Center Groningen, Antonius Deusinglaan 1, 9713, AV, the Netherlands.

Farideh Tabatabaee Yazdi (FT)

Department of Food Science and Technology, Faculty of Agriculture, Ferdowsi University of Mashhad, Mashhad, Iran.

Seyed Ali Mortazavi (SA)

Department of Food Science and Technology, Faculty of Agriculture, Ferdowsi University of Mashhad, Mashhad, Iran. Electronic address: Morteza@um.ac.ir.

Mojtaba Sankian (M)

Immunology Research Center, Bu-Ali Research Institute, School of Medicine, University of Medical Sciences, Mashhad, Iran.

Mahmoud Mahmoudi (M)

Immunology Research Center, Bu-Ali Research Institute, School of Medicine, University of Medical Sciences, Mashhad, Iran.

Fakhri Shahidi (F)

Department of Food Science and Technology, Faculty of Agriculture, Ferdowsi University of Mashhad, Mashhad, Iran.

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Classifications MeSH