Identification of a Novel Proline-Rich Antimicrobial Peptide from Brassica napus.

Proline-rich antimicrobial peptides (PR-AMPs) are a group of cationic host defense peptides that are characterized by a high content of proline residues. Up to now, they have been reported in some insects, vertebrate and invertebrate animals, but are not found in plants. In this study, we performed...

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Main Authors: Huihui Cao, Tao Ke, Renhu Liu, Jingyin Yu, Caihua Dong, Mingxing Cheng, Junyan Huang, Shengyi Liu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4575134?pdf=render
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spelling doaj-a016f9ea3d754a48aac75e2d72e254542020-11-25T01:24:10ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01109e013741410.1371/journal.pone.0137414Identification of a Novel Proline-Rich Antimicrobial Peptide from Brassica napus.Huihui CaoTao KeRenhu LiuJingyin YuCaihua DongMingxing ChengJunyan HuangShengyi LiuProline-rich antimicrobial peptides (PR-AMPs) are a group of cationic host defense peptides that are characterized by a high content of proline residues. Up to now, they have been reported in some insects, vertebrate and invertebrate animals, but are not found in plants. In this study, we performed an in silico screening of antimicrobial peptides, which led to discovery of a Brassica napus gene encoding a novel PR-AMP. This gene encodes a 35-amino acid peptide with 13 proline residues, designated BnPRP1. BnPRP1 has 40.5% identity with a known proline-rich antimicrobial peptide SP-B from the pig. BnPRP1 was artificially synthetized and cloned into the prokaryotic expression vector pET30a/His-EDDIE-GFP. Recombinant BnPRP1 was produced in Escherichia coli and has a predicted molecular mass of 3.8 kDa. Analysis of its activity demonstrated that BnPRP1 exhibited strong antimicrobial activity against Gram-positive bacterium, Gram-negative bacterium, yeast and also had strong antifungal activity against several pathogenic fungi, such as Sclerotinia sclerotiorum, Mucor sp., Magnaporthe oryzae and Botrytis cinerea. Circular dichroism (CD) revealed the main secondary structure of BnPRP1 was the random coil. BnPRP1 gene expression detected by qRT-PCR is responsive to pathogen inoculation. At 48 hours after S. sclerotiorum inoculation, the expression of BnPRP1 increased significantly in the susceptible lines while slight decrease occurred in resistant lines. These suggested that BnPRP1 might play a role in the plant defense response against S. sclerotiorum. BnPRP1 isolated from B. napus was the first PR-AMP member that was characterized in plants, and its homology sequences were found in some other Brassicaceae plants by the genome sequences analysis. Compared with the known PR-AMPs, BnPRP1 has the different primary sequences and antimicrobial activity. Above all, this study gives a chance to cast a new light on further understanding about the AMPs' mechanism and application.http://europepmc.org/articles/PMC4575134?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Huihui Cao
Tao Ke
Renhu Liu
Jingyin Yu
Caihua Dong
Mingxing Cheng
Junyan Huang
Shengyi Liu
spellingShingle Huihui Cao
Tao Ke
Renhu Liu
Jingyin Yu
Caihua Dong
Mingxing Cheng
Junyan Huang
Shengyi Liu
Identification of a Novel Proline-Rich Antimicrobial Peptide from Brassica napus.
PLoS ONE
author_facet Huihui Cao
Tao Ke
Renhu Liu
Jingyin Yu
Caihua Dong
Mingxing Cheng
Junyan Huang
Shengyi Liu
author_sort Huihui Cao
title Identification of a Novel Proline-Rich Antimicrobial Peptide from Brassica napus.
title_short Identification of a Novel Proline-Rich Antimicrobial Peptide from Brassica napus.
title_full Identification of a Novel Proline-Rich Antimicrobial Peptide from Brassica napus.
title_fullStr Identification of a Novel Proline-Rich Antimicrobial Peptide from Brassica napus.
title_full_unstemmed Identification of a Novel Proline-Rich Antimicrobial Peptide from Brassica napus.
title_sort identification of a novel proline-rich antimicrobial peptide from brassica napus.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Proline-rich antimicrobial peptides (PR-AMPs) are a group of cationic host defense peptides that are characterized by a high content of proline residues. Up to now, they have been reported in some insects, vertebrate and invertebrate animals, but are not found in plants. In this study, we performed an in silico screening of antimicrobial peptides, which led to discovery of a Brassica napus gene encoding a novel PR-AMP. This gene encodes a 35-amino acid peptide with 13 proline residues, designated BnPRP1. BnPRP1 has 40.5% identity with a known proline-rich antimicrobial peptide SP-B from the pig. BnPRP1 was artificially synthetized and cloned into the prokaryotic expression vector pET30a/His-EDDIE-GFP. Recombinant BnPRP1 was produced in Escherichia coli and has a predicted molecular mass of 3.8 kDa. Analysis of its activity demonstrated that BnPRP1 exhibited strong antimicrobial activity against Gram-positive bacterium, Gram-negative bacterium, yeast and also had strong antifungal activity against several pathogenic fungi, such as Sclerotinia sclerotiorum, Mucor sp., Magnaporthe oryzae and Botrytis cinerea. Circular dichroism (CD) revealed the main secondary structure of BnPRP1 was the random coil. BnPRP1 gene expression detected by qRT-PCR is responsive to pathogen inoculation. At 48 hours after S. sclerotiorum inoculation, the expression of BnPRP1 increased significantly in the susceptible lines while slight decrease occurred in resistant lines. These suggested that BnPRP1 might play a role in the plant defense response against S. sclerotiorum. BnPRP1 isolated from B. napus was the first PR-AMP member that was characterized in plants, and its homology sequences were found in some other Brassicaceae plants by the genome sequences analysis. Compared with the known PR-AMPs, BnPRP1 has the different primary sequences and antimicrobial activity. Above all, this study gives a chance to cast a new light on further understanding about the AMPs' mechanism and application.
url http://europepmc.org/articles/PMC4575134?pdf=render
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