Evans M, Kaczmarek F S, Stutzman-Engwall K, Dyson P
Molecular Biology Research Group, School of Biological Sciences, University College of Swansea, Singleton Park, UK.
Microbiology (Reading). 1994 Jun;140 ( Pt 6):1367-71. doi: 10.1099/00221287-140-6-1367.
The degradation of Streptomyces avermitilis DNA samples analysed by conventional pulsed-field gel electrophoresis was shown to be due to Tris-dependent, double-strand cleavage. Using alternative electrophoretic conditions, separation of intact DNA molecules was achieved, permitting the identification of two novel giant linear plasmids: the 100 kb pSA1 and 250 kb pSA2. Use of pSA2 DNA as a probe showed that pSA1 does not cross-hybridize, indicating that the plasmids are not closely related. The site-specificity of the DNA modifications, which render the DNA susceptible to Tris-dependent cleavage, was found to be essentially identical to that of similar modifications found in the DNA of S. lividans.
通过常规脉冲场凝胶电泳分析发现,阿维链霉菌DNA样品的降解是由Tris依赖性双链切割所致。采用替代电泳条件,实现了完整DNA分子的分离,从而鉴定出两个新的巨大线性质粒:100 kb的pSA1和250 kb的pSA2。以pSA2 DNA为探针表明,pSA1不会交叉杂交,这表明这些质粒没有密切关系。发现使DNA易受Tris依赖性切割影响的DNA修饰的位点特异性与在淡紫链霉菌DNA中发现的类似修饰基本相同。