首页> 美国卫生研究院文献>Journal of Virology >Transfection of Escherichia coli spheroplasts. VI. Transfection of nonpermissive spheroplasts by T5 and BF23 bacteriophage DNA carrying amber mutations in DNA transfer genes.
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Transfection of Escherichia coli spheroplasts. VI. Transfection of nonpermissive spheroplasts by T5 and BF23 bacteriophage DNA carrying amber mutations in DNA transfer genes.

机译:大肠杆菌原生质球的转染。 VI。 T5和BF23噬菌体DNA在DNA转移基因中携带琥珀色突变从而转染非允许性原生质球。

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摘要

DNA was extracted from T5 and BF23 phage carrying amber mutations in genes A2, A1, or D9 and tested for its ability to transfect su minus spheroplasts. DNA from T5 am231, defective in gene A2, transfects Escherichia coli su minus recB minus spheroplasts with an efficiency of 16% of that of wild-type T5 DNA, whereas DNA from T5 am16d or BF23 am57, both defective in gene A1 or its equivalent, transfects E. coli su minus recB minus spheroplasts with an efficiency of 1.4% of that of wild-type T5 DNA, provided E. coli su+ bacteria is used as the indicator in all cases. More than 95% of the progeny from the am231, am16d, and am57 DNA that transfects su minus recB minus spheroplasts is still amber mutant. From these efficiencies of transfection we conclude that the product of gene A2 functions mainly in the mechanism of transfer of phage DNA to intact host cells, and that this function is not essential for transfection of spheroplasts. We also conclude that gene A1 controls functions in addition to DNA transfer, in agreement with previous studies which show that mutations in gene A1 have a pleiotropic effect. Apparently, the absence of these additional functions controlled by gene A1 leads to a high frequency of abortive infection. DNA from amber mutants defective in either gene A1 or A2 does not appreciably transfect su minus rec+ spheroplasts, indicating that the products of these two genes may both be needed to protect T5 DNA from the very active rec BC nuclease in spheroplasts.
机译:从带有基因A2,A1或D9中琥珀色突变的T5和BF23噬菌体中提取DNA,并测试其转染负原生质球的能力。来自T5 am231的基因A2有缺陷的DNA,以野生型T5 DNA的效率的16%转染了大肠杆菌su recB recB减去原生质球,而来自T5 am16d或BF23 am57的DNA都缺陷了基因A1或同等基因,只要在所有情况下都使用大肠杆菌su +细菌作为指示剂,就可以以野生型T5 DNA的1.4%的效率转染大肠杆菌su recus recB阴性原生质球。来自am231,am16d和am57 DNA的转染Su minus recB minus原生质球的子代中,超过95%的后代仍然是琥珀色突变体。从这些转染效率中,我们得出结论,基因A2的产物主要在噬菌体DNA转移至完整宿主细胞的机制中起作用,并且该功能对于原生质球的转染不是必需的。我们还得出结论,除DNA转移外,基因A1还控制功能,这与先前的研究一致,后者表明基因A1中的突变具有多效作用。显然,基因A1控制的这些附加功能的缺失会导致流产感染的发生率很高。来自基因A1或A2缺陷的琥珀色突变体的DNA不会明显转染负rec +原生质球,表明可能需要这两个基因的产物来保护T5 DNA免受原生质球中非常活跃的rec BC核酸酶的侵害。

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