Beyazova M, Lechevalier M P
Waksman Institute, Rutgers University, Piscataway, New Jersey 08855.
Int J Syst Bacteriol. 1992 Jul;42(3):422-33. doi: 10.1099/00207713-42-3-422.
Low-frequency restriction fragment analysis of more than 100 strains of the genus Frankia showed that restriction enzyme DraI (recognition site, TTT'AAA) gave rise to large DNA fragments (200 to 1,500 kb), which, when they were subjected to cluster analysis, reflected the host plants from which the strains were isolated. Our results support the conclusions of Lalonde and his colleagues (M. Lalonde, L. Simon, J. Bousquet, and A. Seguin, p. 671-680, in H. Bothe, F. J. de Bruijn, and W. E. Newton, ed., Nitrogen Fixation: Hundred Years After, 1988; P. Normand, P. Simonet, and R. Bardin, Mol. Gen. Genet. 213:238-246, 1988) and Fernandez et al. (M. P. Fernandez, H. Meugnier, P. A. D. Grimont, and R. Bardin, Int. J. Syst. Bacteriol. 39:424-429, 1989) that various biochemical and genomic analyses can give rise to groupings of Frankia strains that are consistent with the host plants from which the strains are isolated and that the resulting groups may form a basis for defining Frankia species.
对100多株弗兰克氏菌属菌株进行的低频限制性片段分析表明,限制性内切酶DraI(识别位点为TTT'AAA)产生了大片段DNA(200至1500 kb),当对这些片段进行聚类分析时,反映出了分离出这些菌株的宿主植物。我们的结果支持了拉隆德及其同事(M. 拉隆德、L. 西蒙、J. 布斯凯和A. 塞甘,载于H. 博特、F. J. 德布鲁因和W. E. 牛顿编著的《固氮:百年之后》,1988年,第671 - 680页;P. 诺曼德、P. 西蒙内和R. 巴尔丹,《分子与普通遗传学》213:238 - 246,1988年)以及费尔南德斯等人(M. P. 费尔南德斯、H. 默尼耶、P. A. D. 格里蒙和R. 巴尔丹,《国际系统细菌学杂志》39:424 - 429,1989年)的结论,即各种生化和基因组分析能够产生与分离出这些菌株的宿主植物一致的弗兰克氏菌菌株分组,并且所得到的分组可能构成定义弗兰克氏菌物种的基础。