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J Bacteriol. 1966 Nov;92(5):1378-82. doi: 10.1128/jb.92.5.1378-1382.1966.
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Inhibition of bacterial conjugation by ribonucleic acid and deoxyribonucleic acid male-specific bacteriophages.核糖核酸和脱氧核糖核酸雄性特异性噬菌体对细菌接合的抑制作用。
J Bacteriol. 1968 Feb;95(2):314-26. doi: 10.1128/jb.95.2.314-326.1968.

本文引用的文献

1
Replica plating and indirect selection of bacterial mutants.细菌突变体的影印培养和间接筛选
J Bacteriol. 1952 Mar;63(3):399-406. doi: 10.1128/jb.63.3.399-406.1952.
2
[Sexuality of bacteria].[细菌的性行为]
Boll Ist Sieroter Milan. 1950 Sep-Oct;29(9-10):281-9.
3
Nutritional effects on frequencies of bacterial recombination.营养对细菌重组频率的影响。
J Bacteriol. 1962 Jun;83(6):1332-5. doi: 10.1128/jb.83.6.1332-1335.1962.
4
SYNTHESIS OF BETA-D-GALACTOSIDASE AFTER F-DUCTION OF LAC+GENES INTO ESCHERICHIA COLI.将乳糖操纵子基因导入大肠杆菌后β-D-半乳糖苷酶的合成
J Mol Biol. 1965 Jan;11:23-34. doi: 10.1016/s0022-2836(65)80168-1.
5
GENE TRANSFER BY F' STRAINS OF ESCHERICHIA COLI. IV. EFFECT OF A CHROMOSOMAL DELETION ON CHROMOSOME TRANSFER.大肠杆菌F'菌株介导的基因转移。IV. 染色体缺失对染色体转移的影响。
J Bacteriol. 1964 Aug;88(2):367-73. doi: 10.1128/jb.88.2.367-373.1964.
6
Measurement of activity of single molecules of beta-D-galactosidase.β-D-半乳糖苷酶单分子活性的测量
Proc Natl Acad Sci U S A. 1961 Dec 15;47(12):1981-91. doi: 10.1073/pnas.47.12.1981.
7
Recombination studies of lactose nonfermenting mutants of Escherichia coli K-12.大肠杆菌K-12乳糖非发酵突变体的重组研究。
Genetics. 1962 Oct;47(10):1335-53. doi: 10.1093/genetics/47.10.1335.
8
Fluorogenic substrates for beta-D-galactosidases and phosphatases derived from flurescein (3,6-dihydroxyfluoran) and its monomethylether.源自荧光素(3,6-二羟基荧光黄)及其单甲醚的β-D-半乳糖苷酶和磷酸酶的荧光底物。
Proc Natl Acad Sci U S A. 1963 Jul;50(1):1-6. doi: 10.1073/pnas.50.1.1.
9
Changes during the division cycle in bacterial cell wall synthesis, volume, and ability to concentrate free amino acids.细菌细胞壁合成、体积以及游离氨基酸浓缩能力在分裂周期中的变化。
Biochim Biophys Acta. 1960 Oct 7;43:520-30. doi: 10.1016/0006-3002(60)90474-1.
10
Conjugation and genetic recombination in Escherichia coli K-12.大肠杆菌K-12中的接合与基因重组
Cold Spring Harb Symp Quant Biol. 1956;21:141-62. doi: 10.1101/sqb.1956.021.01.012.

来自大肠杆菌高频重组(Hfr)和F'供体的控制β-D-半乳糖苷酶合成基因的转移与整合

Transfer and incorporation of genes controlling beta-D-galactosidase synthesis from Hfr and F' donors of Escherichia coli.

作者信息

Ganesan A K, Rotman B

出版信息

J Bacteriol. 1966 Nov;92(5):1378-82. doi: 10.1128/jb.92.5.1378-1382.1966.

DOI:10.1128/jb.92.5.1378-1382.1966
PMID:5332400
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC276434/
Abstract

Ganesan, Ann K. (Syntex Institute of Molecular Biology, Palo Alto, Calif.), and Boris Rotman. Transfer and incorporation of genes controlling beta-d-galactosidase synthesis from Hfr and F' donors of Escherichia coli. J. Bacteriol. 92:1378-1382. 1966.-Comparisons were made between Hfr(1) and F(13) donors with respect to the frequency of transfer and incorporation of genes controlling beta-d-galactosidase synthesis. The Hfr(1) donor transfers these genes as part of the chromosome, and the F(13) donor transfers them by F-duction. The criterion used for gene transfer was the acquisition by recipient cells of the ability to synthesize the enzyme, beta-d-galactosidase, measured by fluorogenic assays at the single-cell level. The criterion for incorporation was the formation of lac(+) recombinant colonies. It was found that the two types of donor showed the same frequency of gene transfer, but the probability of incorporation was 10-fold higher in F(13) matings than in Hfr(1) matings. In the former, between 46 and 97% of the merozygotes produced recombinant colonies; in the latter, 2 to 6% did so.

摘要

甘内桑,安·K.(加利福尼亚州帕洛阿尔托市辛泰克斯分子生物学研究所),以及鲍里斯·罗特曼。来自大肠杆菌Hfr和F'供体的控制β - d - 半乳糖苷酶合成基因的转移与整合。《细菌学杂志》92:1378 - 1382。1966年。——就控制β - d - 半乳糖苷酶合成基因的转移频率和整合频率,对Hfr(1)和F(13)供体进行了比较。Hfr(1)供体将这些基因作为染色体的一部分进行转移,而F(13)供体通过F因子转导进行转移。用于基因转移的标准是受体细胞获得合成β - d - 半乳糖苷酶这种酶的能力,通过单细胞水平的荧光测定法来衡量。整合的标准是形成lac(+)重组菌落。结果发现,两种类型的供体显示出相同的基因转移频率,但在F(13)交配中整合的概率比在Hfr(1)交配中高10倍。在前者中,46%至97%的部分二倍体产生了重组菌落;在后者中,这一比例为2%至6%。