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1
Mapping of prophage and mature deoxyribonucleic acid from temperate Bacillus bacteriophage phi 105 by marker rescue.通过标记拯救对温和型芽孢杆菌噬菌体phi 105的原噬菌体和成熟脱氧核糖核酸进行定位
J Virol. 1970 Dec;6(6):760-7. doi: 10.1128/JVI.6.6.760-767.1970.
2
Low-frequency rescue of a genetic marker in deoxyribonucleic acid from Bacillus bacteriophage phi 105 by superinfecting bacteriophage.通过超感染噬菌体对来自芽孢杆菌噬菌体phi 105的脱氧核糖核酸中的遗传标记进行低频拯救。
J Virol. 1970 Dec;6(6):768-71. doi: 10.1128/JVI.6.6.768-771.1970.
3
Heat induction of prophage phi 105 in Bacillus subtilis: replication of the bacterial and bacteriophage genomes.枯草芽孢杆菌中噬菌体phi 105的热诱导:细菌和噬菌体基因组的复制
J Virol. 1971 Oct;8(4):455-68. doi: 10.1128/JVI.8.4.455-468.1971.
4
Structure and biological activity of deoxyribonucleic acid from Bacillus bacteriophage phi 105: effects of Escherichia coli exonucleases.来自芽孢杆菌噬菌体φ105的脱氧核糖核酸的结构与生物活性:大肠杆菌核酸外切酶的作用
J Virol. 1971 Mar;7(3):359-71. doi: 10.1128/JVI.7.3.359-371.1971.
5
Mapping of a temperate bacteriophage active on Bacillus subtilis.一种作用于枯草芽孢杆菌的温和噬菌体的图谱绘制。
J Virol. 1969 Jan;3(1):38-44. doi: 10.1128/JVI.3.1.38-44.1969.
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Characterization of infectious deoxyribonucleic acid from temperature Bacillus subtilis bacteriophage phi105.来自嗜温性枯草芽孢杆菌噬菌体phi105的感染性脱氧核糖核酸的特性分析。
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Mechanism of transfection with deoxyribonucleic acid from the temperate Bacillus bacteriophage phi-105.来自温和型芽孢杆菌噬菌体phi-105的脱氧核糖核酸转染机制。
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Isolation and properties of suppressor-sensitive mutants of Bacillus subtilis bacteriophage SP02.枯草芽孢杆菌噬菌体SP02抑制敏感突变体的分离与特性
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Characterization of inducible bacteriophages in Bacillus licheniformis.地衣芽孢杆菌中可诱导噬菌体的特性分析
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Specific suppression of mutations in genes 46 and 47 by das, a new class of mutations in bacteriophage T4D.噬菌体T4D中的一类新突变das对基因46和47突变的特异性抑制
J Virol. 1971 Nov;8(5):603-12. doi: 10.1128/JVI.8.5.603-612.1971.

引用本文的文献

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Anti-SOS effects induced in Bacillus subtilis by a phi 105 mutant prophage.由phi 105突变前噬菌体在枯草芽孢杆菌中诱导产生的抗SOS效应。
Arch Microbiol. 1993;160(6):486-91. doi: 10.1007/BF00245310.
2
Absence of functional RNA encoded by a silent chromosome in non-complementing diploids obtained from protoplast fusion in Bacillus subtilis.在枯草芽孢杆菌原生质体融合获得的非互补二倍体中,沉默染色体编码的功能性RNA缺失。
Mol Gen Genet. 1983;191(1):81-5. doi: 10.1007/BF00330893.
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Reorienting and expanding the physical map of temperate Bacillus subtilis bacteriophage phi 105.重新定位和扩展温和型枯草芽孢杆菌噬菌体phi 105的物理图谱。
J Bacteriol. 1984 Dec;160(3):1178-80. doi: 10.1128/jb.160.3.1178-1180.1984.
4
Low-frequency rescue of a genetic marker in deoxyribonucleic acid from Bacillus bacteriophage phi 105 by superinfecting bacteriophage.通过超感染噬菌体对来自芽孢杆菌噬菌体phi 105的脱氧核糖核酸中的遗传标记进行低频拯救。
J Virol. 1970 Dec;6(6):768-71. doi: 10.1128/JVI.6.6.768-771.1970.
5
Growth of bacteriophage phi 105 and its deoxyribonucleic acid in radiation-sensitive mutants of Bacillus subtilis.噬菌体φ105及其脱氧核糖核酸在枯草芽孢杆菌辐射敏感突变体中的生长情况。
J Virol. 1971 Dec;8(6):919-21. doi: 10.1128/JVI.8.6.919-921.1971.
6
Heat induction of prophage phi 105 in Bacillus subtilis: replication of the bacterial and bacteriophage genomes.枯草芽孢杆菌中噬菌体phi 105的热诱导:细菌和噬菌体基因组的复制
J Virol. 1971 Oct;8(4):455-68. doi: 10.1128/JVI.8.4.455-468.1971.
7
Unrelatedness of temperate Bacillus subtilis bacteriophages SP02 and phi105.嗜温性枯草芽孢杆菌噬菌体SP02和phi105的非亲缘关系
J Virol. 1972 May;9(5):732-7. doi: 10.1128/JVI.9.5.732-737.1972.
8
Structure of inserted bacteriophage Mu-1 DNA and physical mapping of bacterial genes by Mu-1 DNA insertion.插入的噬菌体Mu-1 DNA的结构以及通过Mu-1 DNA插入对细菌基因进行物理图谱绘制
Proc Natl Acad Sci U S A. 1972 Oct;69(10):2823-7. doi: 10.1073/pnas.69.10.2823.
9
Structure and biological activity of deoxyribonucleic acid from Bacillus bacteriophage phi 105: effects of Escherichia coli exonucleases.来自芽孢杆菌噬菌体φ105的脱氧核糖核酸的结构与生物活性:大肠杆菌核酸外切酶的作用
J Virol. 1971 Mar;7(3):359-71. doi: 10.1128/JVI.7.3.359-371.1971.
10
Mature DNA from temperate bacillusphage phi105 requires primary recombination to be infectious in transfection.来自温和芽孢杆菌噬菌体phi105的成熟DNA在转染中具有感染性需要初级重组。
Mol Gen Genet. 1974;131(4):301-11. doi: 10.1007/BF00264861.

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Localized Negative Interference in Bacteriophage.噬菌体中的局部负干扰
Genetics. 1965 Mar;51(3):369-79. doi: 10.1093/genetics/51.3.369.
2
Characterization of Temperate Bacillus Bacteriophage phi105.温和型芽孢杆菌噬菌体phi105的特性分析
J Virol. 1969 Sep;4(3):264-70. doi: 10.1128/JVI.4.3.264-270.1969.
3
ON THE STRUCTURE OF THE ENDS OF LAMBADA DNA.关于λ噬菌体DNA末端的结构
J Mol Biol. 1965 May;12:36-49. doi: 10.1016/s0022-2836(65)80280-7.
4
Changes in molecular weight of DNA accompanying mutations in phage.噬菌体突变伴随的DNA分子量变化
Proc Natl Acad Sci U S A. 1963 Feb 15;49(2):151-5. doi: 10.1073/pnas.49.2.151.
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A mutation affecting the DNA content of bacteriophage lambda and its lysogenizing properties.一种影响λ噬菌体DNA含量及其溶原化特性的突变。
J Mol Biol. 1961 Aug;3:399-408. doi: 10.1016/s0022-2836(61)80053-3.
6
The transformation of Escherichia coli with deoxyribonucleic acid isolated from bacteriophage lambda-dg.用从噬菌体λ-dg分离的脱氧核糖核酸对大肠杆菌进行转化。
J Mol Biol. 1960 Dec;2:392-415. doi: 10.1016/s0022-2836(60)80050-2.
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A relative molecular weight series derived from the nucleic acid of bacteriophage T2.源自噬菌体T2核酸的相对分子量系列。
J Mol Biol. 1961 Aug;3:458-72. doi: 10.1016/s0022-2836(61)80058-2.
8
The circularity of the phage P22 linkage map.噬菌体P22连锁图谱的环形结构。
Genetics. 1968 Feb;58(2):161-9. doi: 10.1093/genetics/58.2.161.
9
Mutagenic treatment of double- and single-stranded DNA phages T4 ans S13 with hydroxylamine.用羟胺对双链和单链DNA噬菌体T4和S13进行诱变处理。
Virology. 1968 Jun;35(2):330-3. doi: 10.1016/0042-6822(68)90275-4.
10
Low-frequency rescue of a genetic marker in deoxyribonucleic acid from Bacillus bacteriophage phi 105 by superinfecting bacteriophage.通过超感染噬菌体对来自芽孢杆菌噬菌体phi 105的脱氧核糖核酸中的遗传标记进行低频拯救。
J Virol. 1970 Dec;6(6):768-71. doi: 10.1128/JVI.6.6.768-771.1970.

通过标记拯救对温和型芽孢杆菌噬菌体phi 105的原噬菌体和成熟脱氧核糖核酸进行定位

Mapping of prophage and mature deoxyribonucleic acid from temperate Bacillus bacteriophage phi 105 by marker rescue.

作者信息

Armentrout R W, Rutberg L

出版信息

J Virol. 1970 Dec;6(6):760-7. doi: 10.1128/JVI.6.6.760-767.1970.

DOI:10.1128/JVI.6.6.760-767.1970
PMID:5495510
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC376192/
Abstract

By using temperature-sensitive (ts) and suppressor-sensitive (sus) mutants, 11 essential genes have been identified in phage phi105. The order of the genes has been established in two- and three-factor crosses. The genes can be arranged in a linear order; this order is identical in the vegetative phage and in the prophage. One gene essential for phage deoxyribonucleic acid (DNA) synthesis has been found. Marker rescue from prophage and mature DNA, taken up by competent bacteria, was studied by superinfection with phage carrying one sus and one ts mutation. In prophage DNA, all single markers studied are rescued at similar frequencies. The frequency of co-rescue of two markers is proportional to the recombinational distance between the markers. Thus, colinearity between the genetic map and the position on the DNA molecule of those mutations used to establish the map is demonstrated. The results indicate that the recombination frequencies observed in vegetative crosses are a relative measure of the physical distance between markers. All single markers are not rescued at equal frequencies from mature DNA. The frequency of co-rescue of two markers is related to the recombinational distance only over a distance about one-fourth or less of the genetic map. Markers separated by 10% recombination, or more, are co-rescued at 5 to 10% of the frequency of rescue of single markers. Shearing of mature DNA into half-sized molecules reduces the efficiency by which single markers are rescued by a factor of 5 to 10. The results of experiments on co-rescue of two markers from half-sized mature DNA indicate a preferred break-point near the middle of the genetic map; the results are compatible with a nonpermuted sequence in mature DNA. It is pointed out and discussed that mature DNA exhibits several anomalies in marker rescue experiments.

摘要

通过使用温度敏感(ts)和抑制敏感(sus)突变体,在噬菌体phi105中已鉴定出11个必需基因。这些基因的顺序已在双因子和三因子杂交中确定。这些基因可以按线性顺序排列;该顺序在营养噬菌体和原噬菌体中是相同的。已发现一个对噬菌体脱氧核糖核酸(DNA)合成至关重要的基因。通过用携带一个sus和一个ts突变的噬菌体进行超感染,研究了从原噬菌体和成熟DNA中被感受态细菌摄取的标记拯救。在原噬菌体DNA中,所研究的所有单个标记以相似的频率被拯救。两个标记共同拯救的频率与标记之间的重组距离成正比。因此,证明了遗传图谱与用于构建图谱的那些突变在DNA分子上的位置之间的共线性。结果表明,在营养杂交中观察到的重组频率是标记之间物理距离的相对度量。并非所有单个标记从成熟DNA中被拯救的频率都相等。两个标记共同拯救的频率仅在遗传图谱约四分之一或更小的距离范围内与重组距离相关。重组率为10%或更高的标记共同拯救的频率为单个标记拯救频率的5%至10%。将成熟DNA剪切成半大小的分子会使单个标记被拯救的效率降低5至10倍。从半大小的成熟DNA中对两个标记进行共同拯救的实验结果表明,在遗传图谱中间附近有一个优先的断点;结果与成熟DNA中的非置换序列一致。文中指出并讨论了成熟DNA在标记拯救实验中表现出的几个异常现象。