Wehlmann H, Eichenlaub R
Mol Gen Genet. 1980;180(1):205-11. doi: 10.1007/BF00267371.
Proteins specified by the mini-F plasmid (EcoRI restriction fragment f5) were labeled in Escherichia coli minicells and analyzed by SDS-PAGE. Four mini-F encoded proteins could be identified, having molecular weights of 44,000 (A), 36,000 (B), 34,000 (C), and 25,300 (D) daltons. The absence of certain proteins in deleted derivatives of mini-F, generated by treatment with various restriction endonucleases, allowed mapping of the proteins. The A protein maps between F-coordinates 45.7 and 47.9 kb. The gene locus for the B protein is located between 47.2 and 49.3 kb. The C protein maps on a BamHI fragment bordered by F-coordinates 41.5 and 42.8 kb, and finally the D protein maps between 42.8 and 43.8 kb. In addition our data confirm that there are two incompatibility loci on the mini-F genome, located between 45.7 and 47.2 kb (incA) and 44.0 and 45.7 kb (incB). We suggest that (i) the C and D proteins are positive control elements, interacting with origin I and origin II, respectively, (ii) that the incB locus is involved in plasmid partitioning, and (iii) that the A protein encoded by the incA locus is a negative control element.
由微小F质粒(EcoRI限制性片段f5)指定的蛋白质在大肠杆菌微小细胞中进行标记,并通过SDS - PAGE进行分析。可以鉴定出四种由微小F编码的蛋白质,其分子量分别为44,000(A)、36,000(B)、34,000(C)和25,300(D)道尔顿。用各种限制性内切酶处理产生的微小F缺失衍生物中某些蛋白质的缺失,使得能够对这些蛋白质进行定位。A蛋白定位于F坐标45.7至47.9 kb之间。B蛋白的基因座位于47.2至49.3 kb之间。C蛋白定位于一个由F坐标41.5和42.8 kb界定的BamHI片段上,最后D蛋白定位于42.8至43.8 kb之间。此外,我们的数据证实微小F基因组上有两个不相容性位点,分别位于45.7至47.2 kb(incA)和44.0至45.7 kb(incB)之间。我们认为:(i)C和D蛋白是正调控元件,分别与原点I和原点II相互作用;(ii)incB位点参与质粒分配;(iii)由incA位点编码的A蛋白是负调控元件。