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通过伏马菌素B1和B2分析以及核糖体DNA的PCR扩增内转录间隔区的随机扩增多态性DNA(RAPD)和限制性分析对藤仓赤霉菌复合体分离株进行鉴定。

Characterization of Gibberella fujikuroi complex isolates by fumonisin B1 and B2 analysis and by RAPD and restriction analysis of PCR-amplified internal transcribed spacers of ribosomal DNA.

作者信息

Jiménez M, Rodríguez S, Mateo J J, Gil J V, Mateo R

机构信息

Departamento de Microbiología, Facultad de Biología, Universitat de Valencia, Burjassot, Spain.

出版信息

Syst Appl Microbiol. 2000 Dec;23(4):546-55. doi: 10.1016/S0723-2020(00)80029-6.

Abstract

Twenty nine isolates of Fusarium spp. (twenty four of them belonging to the Gibberella fujikuroi complex) isolated from banana and corn from different geographical regions were analyzed for their ability to produce fumonisins B1 and B2 and for genetic relatedness using random amplified polymorphic DNA (RAPD) and restriction analysis of PCR amplification products of the 5.8s ribosomal DNA-intervening internal transcribed spacer regions (ITS I-5.8S-ITS II). For RAPD analysis, six of twenty oligonucleotide primers were selected after testing with five Fusarium spp. isolates and used to characterize 24 additional isolates. DNA fragments from the 29 isolates of Fusarium spp., which were approximately 560 bp, were amplified with the universal primers ITS1 and ITS4. The restriction enzymes HaeIII, MboI, HpaII and MspI were useful for distinguishing the isolates. The RAPD analysis permitted to find interspecific differences among the isolates of Fusarium spp., between isolates with low and high capacity of fumonisin production and among isolates from different hosts. The restriction fragment length polymorphism (RFLP-PCR) analysis permitted to distinguish among different species of Fusarium. In combination with morphological analysis, the results of this research may find an application for the diagnosis of unknown Fusarium spp. and, particularly, for the characterization of fumonisin-producing isolates, which may be very useful in the food technology field.

摘要

对从不同地理区域的香蕉和玉米中分离出的29株镰刀菌属菌株(其中24株属于藤仓赤霉复合体)进行了分析,检测它们产生伏马毒素B1和B2的能力,并使用随机扩增多态性DNA(RAPD)以及对5.8s核糖体DNA间隔区内转录间隔区(ITS I-5.8S-ITS II)的PCR扩增产物进行限制性分析来研究其遗传相关性。对于RAPD分析,在对5株镰刀菌属菌株进行测试后,从20个寡核苷酸引物中选择了6个,并用于鉴定另外24株菌株。用通用引物ITS1和ITS4扩增了29株镰刀菌属菌株中约560 bp的DNA片段。限制性内切酶HaeIII、MboI、HpaII和MspI可用于区分这些菌株。RAPD分析能够发现镰刀菌属菌株之间、伏马毒素产生能力高低不同的菌株之间以及来自不同宿主的菌株之间的种间差异。限制性片段长度多态性(RFLP-PCR)分析能够区分不同的镰刀菌物种。结合形态学分析,本研究结果可能在未知镰刀菌属物种的诊断中得到应用,特别是在产伏马毒素菌株的鉴定方面,这在食品技术领域可能非常有用。

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