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首页> 外文期刊>Journal of Virology >Phi W-14 DNA inhibits transfection of Bacillus subtilis by SPP1 DNA.
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Phi W-14 DNA inhibits transfection of Bacillus subtilis by SPP1 DNA.

机译:PHI W-14 DNA通过SPP1 DNA抑制枯草芽孢杆菌的转染。

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摘要

The DNA of bacteriophage phi W-14 is unusual in that half of the thymine residues are replaced with the hypermodified pyrimidine alpha-putrescinylthymine (Kropinski et al., Biochemistry 12:151-157, 1973). Bacteriophage phi W-14 DNA and Bacillus subtilis DNA exhibited comparable competing abilities for the uptake of transfecting bacteriophage SPP1 DNA by competent cells of B. subtilis. B. subtilis DNA decreased transfection and uptake to the same extent, indicating that it merely competed with SPP1 DNA for uptake. Phi W-14 DNA, however, decreased transfection up to 30 times more effectively than it inhibited uptake. Phi W-14 DNA did not alter the kinetics of transfection. The degree of inhibition of transfection was dependent upon the time of addition of Phi W-14 DNA relative to the time of addition of SPP1 DNA. If failed to inhibit when added 30 min after SPP1 DNA. It had a fourfold-greater effect when added 10 min before, rather than simultaneously with, SPP1, but this enhancement was abolished by high concentrations of SPP1 DNA. The nature of the transfection process was not altered in those cells escaping inhibition by Phi W-14 DNA: two molecules of transfecting SPP1 DNA were required to form a transfectant with or without Phi W-14 DNA. Free putrescine did not affect transfection by SPP1 DNA. It was concluded that the putrescine groups covalently attached to phi W-14 DNA allowed this DNA to interfere with the transfection process at the intracellular level.
机译:噬菌体PHI W-14的DNA在该一半的胸腺嘧啶残留物中是不寻常的,用高浆化嘧啶α-普普芳基(Kropinski等,生物化学12:151-157,1973)取代。噬菌体PHI W-14 DNA和枯草芽孢杆菌DNA表现出通过B.枯草芽孢杆菌的能量细胞转染噬菌体SPP1 DNA的相应竞争能力。 B.枯草芽孢杆菌DNA在相同程度上减少转染和摄取,表明它仅与SPP1 DNA竞争以进行摄取。然而,PHI W-14 DNA,比抑制摄取量更有效地减少了转染后30倍。 PHI W-14 DNA没有改变转染的动力学。转染的抑制程度取决于相对于加入SPP1 DNA的时间的PHI W-14 DNA的时间。如果在SPP1 DNA后30分钟加入时未能抑制。当前添加10分钟而不是SPP1时,它具有四倍更大的效果,但通过高浓度的SPP1 DNA废除了这种增强。转染过程的性质在通过PHI W-14 DNA逸出的那些细胞中未改变:需要两种转染SPP1 DNA的分子,以形成有或没有PHI W-14 DNA的转染剂。自由腐败管道没有影响SPP1 DNA的转染。得出结论是,共价连接到PHI W-14 DNA的Putrescine基团使该DNA干扰细胞内水平的转染过程。

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