Das Gupta C K, Vrancic A, Guha A
Gene. 1977 Jul;1(5-6):331-45. doi: 10.1016/0378-1119(77)90038-5.
DNA containing the biotin gene cluster, bioABFCD, of E. coli K-12 has been isolated from the EcoRI cleavage products of lambdabiot124-10 phage DNA and subsequently characterized by electron microscopic studies. The biotin-DNA fragment obtained after EcoRI cleavage of the lambdabiot124-10 DNA measures 18.7% lambda DNA length (approx. 9000 base pairs). In addition to the biotin genes, it contains 4.75% and 3.08% lambda phage DNA at the left and right end-points of the bioABFCD cluster, respectively. The two bio promoter sites of the divergently transcribed biotin genes have been visualized under the electron microscope by binding RNA polymerase holoenzyme to the biotin DNA fragment. The two promoters are located at 41% and 43% length of the DNA fragment from its left endpoint. In vitro transcription of RNA from the bio-tin-DNA fragment has been visualized with the electron microscope, but so far no simultaneously transcribing "RNA:DNA" loops of the divergently oriented genes have been observed.
含有大肠杆菌K - 12生物素基因簇bioABFCD的DNA已从λbiot124 - 10噬菌体DNA的EcoRI切割产物中分离出来,随后通过电子显微镜研究进行了表征。λbiot124 - 10 DNA经EcoRI切割后获得的生物素 - DNA片段长度为λDNA长度的18.7%(约9000个碱基对)。除了生物素基因外,它在bioABFCD簇的左端和右端分别包含4.75%和3.08%的λ噬菌体DNA。通过将RNA聚合酶全酶与生物素DNA片段结合,在电子显微镜下观察到了双向转录的生物素基因的两个生物启动子位点。这两个启动子位于DNA片段从其左端起长度的41%和43%处。已通过电子显微镜观察到从生物素 - DNA片段体外转录RNA的情况,但到目前为止尚未观察到双向定向基因同时转录的“RNA:DNA”环。