Steinhart W L, Herriott R M
J Bacteriol. 1968 Nov;96(5):1718-24. doi: 10.1128/jb.96.5.1718-1724.1968.
During genetic transformation of Haemophilus influenzae, segments of the host deoxyribonucleic acid (DNA) corresponding to the integrating donor DNA were degraded and liberated into the medium. This degradation was detected by the release of the radioactive label from host DNA during a time period matching the time of development of maximal linkage between donor and host markers. The host label released above that released from nontransformed, control cultures was equivalent to about 2% of the host genome or 16 x 10(6) daltons of DNA. The released, labeled material was acid-soluble and dialyzable. The label release from control cultures was unaffected at 30 C; at this temperature, the recombination-specific release from transformed cells was suppressed. High molecular weight fragments of host DNA corresponding in size to the donor fragments could not be found free within the cell, weakly bound to other host DNA, or bound to non-integrated donor DNA by a reciprocal cross mechanism.
在流感嗜血杆菌的基因转化过程中,与整合的供体DNA相对应的宿主脱氧核糖核酸(DNA)片段被降解并释放到培养基中。这种降解是通过在与供体和宿主标记之间最大连锁发展时间相匹配的时间段内,宿主DNA中放射性标记的释放来检测的。从转化细胞中释放的宿主标记物超过未转化的对照培养物中释放的量,相当于宿主基因组的约2%或16×10⁶道尔顿的DNA。释放的标记物质可溶于酸且可透析。在30℃时,对照培养物中的标记物释放不受影响;在此温度下,转化细胞中重组特异性释放受到抑制。在细胞内未发现与供体片段大小相对应的宿主DNA高分子量片段游离存在,也未发现其与其他宿主DNA弱结合或通过相互交叉机制与未整合的供体DNA结合。