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An assessment of the genetic diversity within Ganoderma strains with AFLP and ITS PCR-RFLP.

机译:用AFLP和ITS PCR-RFLP评估灵芝菌株内的遗传多样性。

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摘要

Ganoderma lucidum is one of the most important medicinal materials and plant pathogens. Because of its specific interhybridization, the genetic background, however, is relatively unclear. It made identification of Ganoderma strains, especially closely related strains difficulty. Amplified fragment length polymorphism (AFLP) using 14 primer combinations and internal transcribed spacer (ITS) PCR-RFLP were used in a comparative study which was designed to investigate the closely related Ganoderma strains genetic relations at molecular level. The analysis of 37 Ganoderma strains showed there were 177 polymorphic AFLP markers and 12 ITS PCR-RFLP markers, and all accessions could be uniquely identified. Among the Ganoderma accessions, similarity coefficients ranged from 0.07692 to 0.99194 in AFLP. The Ganoderma strains formed a tight cluster in nine groups in AFLP whereas seven groups in ITS PCR-RFLP. The cluster analysis revealed that the taxonomical system of subgenus Ganoderma is composed of Sect. Ganoderma and Sect. Phaeonema, and the strain 22 should be a variant form of strain 21. All methods delineated the Ganoderma strains from the different regions seeming to show a greater level of genetic diversity. It indicated that the genotype study at molecular level is a useful complement method to the current classification system of Ganoderma strains based on morphological traits. The congruency of the experiments was analyzed using the biostatistical software DPS V3.01.
机译:灵芝是最重要的药用材料和植物病原体之一。由于其特定的杂种杂交,遗传背景相对不清楚。它使灵芝菌株的鉴定,特别是与之密切相关的菌株的鉴定变得困难。使用14个引物组合和内部转录间隔区(ITS)PCR-RFLP扩增片段长度多态性(AFLP),用于在分子水平上研究密切相关的灵芝菌株遗传关系。对37株灵芝菌株的分析显示,有177个多态性AFLP标记和12个ITS PCR-RFLP标记,所有种质均可唯一鉴定。在灵芝品种中,AFLP的相似系数范围为0.07692至0.99194。 灵芝菌株在AFLP中分为9组,而在ITS PCR-RFLP中则为7组。聚类分析表明,灵芝亚属的分类系统由Sect组成。 灵芝和Sect。 Phaeonema ,菌株22应该是菌株21的变体形式。所有方法都描述了似乎显示出更高遗传多样性水平的不同地区的 Ganoderma 菌株。这表明在分子水平上进行基因型研究是对基于形态学特征的灵芝菌株当前分类系统的一种有用的补充方法。使用生物统计软件DPS V3.01分析了实验的一致性。

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