Abou-Sabé M, Pilla J, Hazuda D, Ninfa A
J Bacteriol. 1982 May;150(2):762-9. doi: 10.1128/jb.150.2.762-769.1982.
The D-ribose operon (rbs) of Escherichia coli K-12 maps at 83 min and is inducible. The rbs operon of E. coli B/r maps at 2 min and is constitutive. Evidence is presented showing that a second inducible copy of the rbs operons is present in E. coli B/r mapping at 83 min. The data indicated that the duplication of the rbs operon represented a transposition of the 83-min region to 2 min. The identification of a second copy of the rbs operon in B/r and the determination of its inducibility were based on the reactivation, through mutagenesis, of inducible rbs expression, mapping by P1 transduction of the mutation site to 83 min, and merodiploid complementation analysis of the D-ribokinase expression in E. coli B/r. We also show that the rbs transposition to 2-min continued to generate transposable elements coding for the 1- to 2-min region of the chromosome and transposing onto extrachromosomal DNA target molecules such as pBR322.
大肠杆菌K-12的D-核糖操纵子(rbs)定位在83分钟处,是可诱导的。大肠杆菌B/r的rbs操纵子定位在2分钟处,是组成型的。本文提供的证据表明,在大肠杆菌B/r中,83分钟处存在rbs操纵子的第二个可诱导拷贝。数据表明,rbs操纵子的重复代表了83分钟区域向2分钟区域的转座。在B/r中鉴定出rbs操纵子的第二个拷贝并确定其可诱导性,是基于通过诱变重新激活可诱导的rbs表达、通过P1转导将突变位点定位到83分钟以及对大肠杆菌B/r中D-核糖激酶表达进行部分二倍体互补分析。我们还表明,rbs向2分钟区域的转座继续产生编码染色体1至2分钟区域的转座元件,并转座到诸如pBR322等染色体外DNA靶分子上。