Wolska K I, Kunicki-Goldfinger W J
Acta Microbiol Pol. 1977;26(4):325-35.
Polarity of donor DNA strand transferred into recipient during conjugation in Escherichia coli K-12 was determined by DNA-3H-RNA hybridization. Lambda prophage was used as a marker. The defective lysogen Hfr H (lambdat11) as a donor and thermosensitive F- CR34 dnaB strain as recipient were used. Two sets of hybridization experiments, with 1-strand specific lambda mRNA and lambda mRNA specific for both phage strands but with large excess of r-strand specific mRNA, were carried out. Strand 1 of lambda DNA was detected preferentially in recipient cells mated at restrictive temperature, when Hfr transferred its genophore in the order gal-lambda-bio. Thus the genophore is transferred with 5'OH at its origin.
通过DNA - 3H - RNA杂交确定了在大肠杆菌K - 12接合过程中转移到受体中的供体DNA链的极性。λ原噬菌体用作标记物。使用缺陷溶原菌Hfr H(λt11)作为供体,热敏性F - CR34 dnaB菌株作为受体。进行了两组杂交实验,一组使用单链特异性λmRNA,另一组使用对噬菌体两条链均特异但r链特异性mRNA大量过量的λmRNA。当Hfr按gal - λ - bio顺序转移其基因载体时,在限制温度下交配的受体细胞中优先检测到λDNA的1链。因此,基因载体以其起始端的5'OH进行转移。