Peptidomic Analysis and Antimicrobial Activity of Serum Peptide from Hevea brasiliensis Clone BPM24.

IF 1 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Phattara-Orn Havanapan, Supaporn Ieamkhang, Nuanwan Phungthanom, Walairat Bourchookarn, Apichai Bourchookarn, Chartchai Krittanai
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引用次数: 0

Abstract

Background: Hevea brasiliensis is severely affected by the fungal disease caused by Phytophthora spp. Significant loss of rubber yield is widespread and extensive use of chemical fungicides has resulted in health and environmental problems.

Objective: This work aims to extract and identify the latex serum peptides from a disease tolerant clone of H. brasiliensis, and study the inhibitory efficacy against pathogenic bacteria and fungi.

Methods: Serum peptides were extracted from H. brasiliensis BPM24 using mixed lysis solution. Low molecular weight peptides were screened and fractionated by solid-phase extraction and then identified by tandem mass spectrometry. Total and fractionated serum peptides were assayed for bacterial and fungal inhibition using broth microdilution and poisoned food methods. An inhibitory control study in the greenhouse was also performed using susceptible clones for pre and postinfection with Phytophthora spp.

Results: Forty-three serum peptide sequences were successfully identified. Thirty-four peptides matched with the proteins associated with plant defense response signaling, host resistance, and adverse environmental factors. The inhibitory study of total serum peptides demonstrated antibacterial and anti-fungal properties. The greenhouse study exhibited disease inhibitory efficacy of 60% for the treatment of Phytophthora spp. in post-infected plants and 80% for pre-treated samples.

Conclusion: Latex serum peptides from disease tolerant H. brasiliensis revealed several proteins and peptides associated with plant defense and disease resistance. The peptides play a vital role for defense against bacteria and fungi pathogens, including Phytophthora spp. Enhanced disease protection can be obtained when the extracted peptides were applied to the susceptible plants before exposure to the fungi. These findings provided an insight and may pave the way for the development of biocontrol peptides from natural resources.

巴西橡胶树克隆BPM24血清肽的肽组学分析及抗菌活性研究。
背景:橡胶树是巴西橡胶树(Hevea brasiliensis)受疫霉(Phytophthora spp)真菌病害的严重病害,橡胶树产量损失严重,化学杀菌剂的大量使用造成了健康和环境问题。目的:从巴西芽孢杆菌耐病克隆中提取并鉴定乳胶乳血清肽,研究其对病原菌和真菌的抑制作用。方法:采用混合裂解液提取巴西血吸虫BPM24血清多肽。采用固相萃取法对低分子量肽进行筛选和分离,并用串联质谱法进行鉴定。用微量肉汤稀释法和中毒食品法测定血清总肽和分离肽对细菌和真菌的抑制作用。结果:成功鉴定了43个血清肽序列。34个多肽与植物防御应答信号、宿主抗性和不利环境因子相关的蛋白质相匹配。对血清总肽的抑制研究显示出抗菌和抗真菌的特性。温室研究表明,对疫霉侵染后的植株和处理前的样品的抑制效果分别为60%和80%。结论:从耐病巴西螺的乳胶血清肽中发现了与植物防御和抗病相关的多种蛋白和肽。这些肽在抵抗细菌和真菌病原体(包括疫霉)中起着至关重要的作用,在暴露于真菌之前将提取的肽涂在易感植物上可以获得增强的疾病保护作用。这些发现为从自然资源中开发生物防治肽提供了新的思路和途径。
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来源期刊
Protein and Peptide Letters
Protein and Peptide Letters 生物-生化与分子生物学
CiteScore
2.90
自引率
0.00%
发文量
98
审稿时长
2 months
期刊介绍: Protein & Peptide Letters publishes letters, original research papers, mini-reviews and guest edited issues in all important aspects of protein and peptide research, including structural studies, advances in recombinant expression, function, synthesis, enzymology, immunology, molecular modeling, and drug design. Manuscripts must have a significant element of novelty, timeliness and urgency that merit rapid publication. Reports of crystallization and preliminary structure determination of biologically important proteins are considered only if they include significant new approaches or deal with proteins of immediate importance, and preliminary structure determinations of biologically important proteins. Purely theoretical/review papers should provide new insight into the principles of protein/peptide structure and function. Manuscripts describing computational work should include some experimental data to provide confirmation of the results of calculations. Protein & Peptide Letters focuses on: Structure Studies Advances in Recombinant Expression Drug Design Chemical Synthesis Function Pharmacology Enzymology Conformational Analysis Immunology Biotechnology Protein Engineering Protein Folding Sequencing Molecular Recognition Purification and Analysis
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