Simon L, Lalonde M, Bruns T D
Faculté de Foresterie et de Géomatique, Université Laval, Sainte-Foy, Québec, Canada.
Appl Environ Microbiol. 1992 Jan;58(1):291-5. doi: 10.1128/aem.58.1.291-295.1992.
The first DNA sequences obtained from arbuscular endomycorrhizal fungi are reported. They were obtained by directly sequencing overlapping amplified fragments of the nuclear genes coding for the small subunit rRNA. These sequences were used to develop a polymerase chain reaction primer (VANS1) that enables the specific amplification of a portion of the vesicular-arbuscular endomycorrhizal fungus small subunit rRNA directly from a mixture of plant and fungal tissues. The specificity of this primer for arbuscular endomycorrhizal fungi was demonstrated by testing it on a number of organisms and by sequencing the fragment amplified from colonized leek (Allium porum) roots. This approach, coupled with other molecular techniques, will facilitate rapid detection, identification, and possibly quantitation of arbuscular endomycorrhizal fungi.
首次报道了从丛枝内生菌根真菌中获得的DNA序列。这些序列是通过对编码小亚基rRNA的核基因的重叠扩增片段进行直接测序而获得的。这些序列被用于开发一种聚合酶链反应引物(VANS1),该引物能够直接从植物和真菌组织的混合物中特异性扩增丛枝内生菌根真菌小亚基rRNA的一部分。通过在多种生物体上进行测试,并对从定殖的韭菜(葱属)根中扩增的片段进行测序,证明了该引物对丛枝内生菌根真菌的特异性。这种方法与其他分子技术相结合,将有助于快速检测、鉴定以及可能对丛枝内生菌根真菌进行定量分析。