Notani N, Goodgal S H
J Gen Physiol. 1966 Jul;49(6):197-209. doi: 10.1085/jgp.49.6.197.
During the process of transformation in Hemophilus influenzae integration of donor DNA, i.e. the formation of recombinant DNA, involves the incorporation of single-stranded DNA. Evidence was obtained from cesium chloride density gradient centrifugation of DNA from donor-recipient complexes that integration was accompanied by the formation of hybrid DNA with a density intermediate with respect to heavy, (2)H, (15)N, donor and light, (1)H, (4)N recipient DNA. On denaturation the position of the heavy donor DNA moved closer to, but not all the way toward, the density position of the original donor DNA. In addition to supporting the idea of single-stranded incorporation, this evidence suggested that the integrated donor DNA was covalently linked to light recipient DNA. The DNA was taken up in the double-stranded form and no detectable amounts of denatured DNA could be found during the transformation process. However, during the process of integration an amount of donor atoms, equivalent to the amount of hybrid DNA formed, appeared in recipient DNA, and indicated that while one strand of DNA was integrated the other was broken down and resynthesized. The density of the hybrid DNA, as well as rebanding of denatured hybrid, indicated that the size of the integrated piece of DNA was large, approximately 6 x 10(6) daltons.
在流感嗜血杆菌转化过程中,供体DNA的整合,即重组DNA的形成,涉及单链DNA的掺入。从供体 - 受体复合物的DNA经氯化铯密度梯度离心获得的证据表明,整合伴随着形成密度介于重的(2)H、(15)N供体DNA和轻的(1)H、(4)N受体DNA之间的杂种DNA。变性后,重的供体DNA的位置向原来供体DNA的密度位置移动,但并未完全移至该位置。除了支持单链掺入的观点外,这一证据还表明整合的供体DNA与轻的受体DNA共价相连。DNA以双链形式被摄取,在转化过程中未发现可检测到的变性DNA量。然而,在整合过程中,相当于形成的杂种DNA量的供体原子量出现在受体DNA中,这表明当一条DNA链被整合时,另一条链被分解并重新合成。杂种DNA的密度以及变性杂种的重新带型表明,整合的DNA片段大小很大,约为6×10⁶道尔顿。