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Summary Three types of minicircular DNA isolated from Vicia faba mitochondria were cloned in pBR322 plasmids. The correspondence of cloned sequences to the original molecules was verified by coelectrophoresis and by DNA-DNA hybridization with total mitochondrial DNA preparations. It was found that the cloned sequences hybridized not only with the minicirclar DNAs and their derivates, but also with some discrete classes of higher molecular weight DNA and with the major DNA. The data obtained from restriction enzyme analysis of complementary sequences suggested that the majority of them were represented by the minicircular DNAs and by the oligomers. The physical maps of cloned sequences were also prepared. These maps differed significantly. However, reciprocal DNA-DNA hybridization showed the existence of sequence homology between minicircular DNAs.  相似文献   
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In a culture of filamentous cyanobacteriumMicrocoleus chthonoplastes under high phosphorus content and the presence of NaF, formation of aggregated microtubes of 0.8–1.0 m in diameter was obtained. Microtubes contain calcium and phosphorus. These filamentous structures do not represent fossilized bacteria.  相似文献   
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In cells of L1210 ascite leukemia cells, methotrexate inhibited H3-thymidine incorporation, blocked shortly (during 4 hours) the G1 leads to S transition, and did not affect cells in G2-phase or in the late S phase. Almost half a cell population was degenerated and cells in S- and G1-phases were affected in equal proportion. This may suggest that methotrexate is not S-phase specific for cells of leukemia L1210. A simultaneous administration of vinblastine increases the antitumour effect of methotrexate. Cells in G2-phase constitute, presumably, a significant proportion of cells recovered after methotrexate administration. A comparison of the data obtained with literature evidence shows that in the sensitive (leukemia L1210) and resistant (acute mieloid leukemia of man) forms of leukemia, methotrexate affects cells that are in S-phase, whereas cells being in G1-phase are affected only when the sensitive tumours are treated.  相似文献   
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The difference in the growth on fructose between differentiated and adifferentiated variants of Streptomyces roseoflavus var. roseofungini should be attributed to their different capacity in forming the enzyme system for fructose uptake whose action is induced by this carbohydrate. In the cells of the two variants grown on glucose and mannitol, the process of induction occurs in the presence of chloramphenicol. In the cells grown on glycerol, chloramphenicol inhibits the induction. The growth of the differentiated variant on fructose stops apparently due to the exhaustion of endogenous reserves which are necessary for maintaining the system of fructose uptake in the active state.  相似文献   
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