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首页> 外文期刊>Postharvest Biology and Technology >Isolation and characterization of Bacillus amyloliquefaciens PG12 for the biological control of apple ring rot
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Isolation and characterization of Bacillus amyloliquefaciens PG12 for the biological control of apple ring rot

机译:解淀粉芽孢杆菌PG12的分离及鉴定苹果环腐病的生物防治

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摘要

Bacillus spp. are promising candidates for biological control of postharvest diseases. Bacillus amyloliquefaciens PG12 was isolated from apple fruit and exhibited broad-spectrum antifungal activity. Botryosphaeria dothidea was significantly suppressed by PG12 in in vitro and in vivo. Lumpy appearance and abnormal structure of the mycelia from the edge of inhibition zone were observed using scanning electron microscopy (SEM) in in vitro assays. Furthermore, the lipopeptide crude extracts from cell-free supernatant of PG12 had remarkable antifungal activity against B. dothidea, indicating that lipopeptides played a major role in the biological control ability of PG12. PCR detection revealed that PG12 harbored the gene clusters required for the biosynthesis of the two main families of lipopeptide, including iturin and fengycin. One iturin-like compound (R-f 0.4) showed inhibitory activity against B. dothidea using thin layer chromatography (TLC)-bioautography analysis and were further fractionated by semipreparative high performance liquid chromatography (HPLC). The fraction with a molecular weight of 1043.55 m/z was identified as iturin A by electrospray ionization quadrupole-time-of-flight mass spectrometry/mass spectrometry (ESI-Q-TOF MS). Taken together, B. amyloliquefaciens PG12 was an effective biocontrol agent against apple ring rot caused by B. dothidea and iturin A was an important factor in its activity. (C) 2015 Elsevier B.V. All rights reserved.
机译:芽孢杆菌是收获后疾病生物防治的有前途的候选人。从苹果果实中分离出解淀粉芽孢杆菌PG12,并表现出广谱抗真菌活性。 PG12在体外和体内均显着抑制了灰葡萄孢。在体外测定中使用扫描电子显微镜(SEM)观察到了来自抑制区边缘的菌丝体的块状外观和异常结构。此外,从无细胞的PG12上清液中提取的脂肽粗提物对双歧杆菌具有显着的抗真菌活性,这表明脂肽在PG12的生物学控制能力中起着重要作用。 PCR检测显示PG12含有生物合成两个主要脂肽家族(包括伊图林和丰霉素)所需的基因簇。使用薄层色谱(TLC)-生物自显影分析法,一种类尿嘧啶样化合物(R-f 0.4)显示出对双歧杆菌的抑制活性,并通过半制备高效液相色谱(HPLC)进一步分离。通过电喷雾电离四极杆飞行时间质谱/质谱(ESI-Q-TOF MS)将分子量为1043.55 m / z的馏分鉴定为iturinA。总的来说,解淀粉芽孢杆菌PG12是一种有效的生物防治剂,可抵抗由多头芽孢杆菌引起的苹果环腐病,而木兰素A是其活性的重要因素。 (C)2015 Elsevier B.V.保留所有权利。

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