Shams Marzieh Varasteh, Nazarian-Firouzabadi Farhad, Ismaili Ahmad, Shirzadian-Khorramabad Reza
Agronomy and Plant Breeding Department, Faculty of Agriculture, Lorestan University, Khorramabad, Iran.
Department of Agricultural Biotechnology, Faculty of Agricultural Sciences, University of Guilan, Rasht, 4199613776, Iran.
Mol Biotechnol. 2019 Apr;61(4):241-252. doi: 10.1007/s12033-019-00153-x.
Expression of strong antimicrobial peptides in plants is of great interest to combat a wide range of plant pathogens. To bring the Dermaseptin B1 (DrsB1) peptide to the intimate contact of the plant pathogens cell wall surface, the DrsB1 encoding sequence was fused to the C-terminal part of the two copies of the chitin-binding domain (CBD) of the Avr4 effector protein and used for Agrobacterium rhizogenes-mediated transformation. The expression of the recombinant protein in the tobacco hairy roots (HRs) was confirmed by molecular analysis. Antimicrobial activity analysis of the recombinant protein purified from the transgenic HRs showed that the (CBD)2-DrsB1 recombinant protein had a significant (p < 0.01) antimicrobial effect on the growth of different fungal and bacterial pathogens. The results of this study indicated that the recombinant protein had a higher antifungal activity against chitin-producing Alternaria alternata than Pythium spp. Scanning electron microscopy images demonstrated that the recombinant protein led to fungal hypha deformation, fragmentation, and agglutination of growing hypha, possibly by dissociating fungal cell wall components. In vitro evidences suggest that the expression of the (CBD)2-DrsB1 recombinant protein in plants by generating transgenic lines is a promising approach to produce disease-resistant plants, resistance to chitin-producing pathogenic fungi.
在植物中表达强效抗菌肽对于对抗多种植物病原体具有重要意义。为了使皮肤抗菌肽B1(DrsB1)肽与植物病原体细胞壁表面紧密接触,将DrsB1编码序列与Avr4效应蛋白的两个几丁质结合结构域(CBD)的C末端部分融合,并用于发根农杆菌介导的转化。通过分子分析证实了重组蛋白在烟草毛状根(HRs)中的表达。对从转基因HRs中纯化的重组蛋白进行的抗菌活性分析表明,(CBD)2-DrsB1重组蛋白对不同真菌和细菌病原体的生长具有显著(p <0.01)的抗菌作用。本研究结果表明,重组蛋白对产几丁质的链格孢的抗真菌活性高于腐霉菌。扫描电子显微镜图像显示,重组蛋白可能通过解离真菌细胞壁成分导致真菌菌丝变形、断裂和生长菌丝凝集。体外证据表明,通过产生转基因系在植物中表达(CBD)2-DrsB1重组蛋白是培育抗病植物(对产几丁质致病真菌具有抗性)的一种有前景的方法。