Jarausch W, Saillard C, Dosba F, Bové J M
Station de Recherches Fruitières, Institut National de la Recherche Agronomique, Bordeaux, France.
Appl Environ Microbiol. 1994 Aug;60(8):2916-23. doi: 10.1128/aem.60.8.2916-2923.1994.
A 1.8-kb chromosomal DNA fragment of the mycoplasmalike organism (MLO) associated with apple proliferation was sequenced. Three putative open reading frames were observed on this fragment. The protein encoded by open reading frame 2 shows significant homologies with bacterial nitroreductases. From the nucleotide sequence four primer pairs for PCR were chosen to specifically amplify DNA from MLOs associated with European diseases of fruit trees. Primer pairs specific for (i) Malus-affecting MLOs, (ii) Malus- and Prunus-affecting MLOs, and (iii) Malus-, Prunus-, and Pyrus-affecting MLOs were obtained. Restriction enzyme analysis of the amplification products revealed restriction fragment length polymorphisms between Malus-, Prunus, and Pyrus-affecting MLOs as well as between different isolates of the apple proliferation MLO. No amplification with either primer pair could be obtained with DNA from 12 different MLOs experimentally maintained in periwinkle.
对与苹果增殖相关的类支原体生物(MLO)的一个1.8 kb染色体DNA片段进行了测序。在该片段上观察到三个推定的开放阅读框。开放阅读框2编码的蛋白质与细菌硝基还原酶具有显著同源性。根据核苷酸序列选择了四对PCR引物,以特异性扩增与欧洲果树病害相关的MLO的DNA。获得了分别针对(i)影响苹果的MLO、(ii)影响苹果和李属的MLO以及(iii)影响苹果、李属和梨属的MLO的引物对。扩增产物的限制性酶切分析揭示了影响苹果、李属和梨属的MLO之间以及苹果增殖MLO的不同分离株之间的限制性片段长度多态性。用长春花中实验保存的12种不同MLO的DNA,使用任何一对引物均未获得扩增产物。