Ream L W, Margossian L, Clark A J, Hansen F G, von Meyenburg K
Mol Gen Genet. 1980;180(1):115-21. doi: 10.1007/BF00267359.
Two factor transductional crosses place recF at approximately 82 min on the E. coli chromosome; recF is highly cotransducible with dnaA and gyrB (cou). Transductional analysis with a series of lambda tna specialized transducing phages carrying chromosomal DNA from the tnaA region place recF between dnaA and gyrB. This analysis also indicates that a gene lying in the same region and producing an easily detectable protein (estimated MW of 45 kD) is dnaN and not recF.
两因子转导杂交实验将recF定位在大肠杆菌染色体上约82分钟处;recF与dnaA和gyrB(cou)高度共转导。利用一系列携带来自tnaA区域染色体DNA的λtna特异性转导噬菌体进行转导分析,结果表明recF位于dnaA和gyrB之间。该分析还表明,位于同一区域且产生一种易于检测的蛋白质(估计分子量为45 kD)的基因是dnaN而非recF。