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1
Relationship of Bacillus subtilis DNA polymerase III to bacteriophage PBS2-induced DNA polymerase and to the replication of uracil-containing DNA.枯草芽孢杆菌DNA聚合酶III与噬菌体PBS2诱导的DNA聚合酶的关系以及与含尿嘧啶DNA复制的关系。
J Virol. 1978 Dec;28(3):697-709. doi: 10.1128/JVI.28.3.697-709.1978.
2
Bacillus subtilis DNA polymerase III is required for the replication of DNA of bacteriophages SPP-1 and phi 105.枯草芽孢杆菌DNA聚合酶III是噬菌体SPP - 1和phi 105的DNA复制所必需的。
J Virol. 1977 Feb;21(2):493-6. doi: 10.1128/JVI.21.2.493-496.1977.
3
Resistance of bacteriophage PBS2 infection to 6-(p-hydroxyphenylazo)-uracil, an inhibitor of Bacillus subtilis deoxyribonucleic acid synthesis.噬菌体PBS2感染对6-(对羟基苯偶氮)尿嘧啶(一种枯草芽孢杆菌脱氧核糖核酸合成抑制剂)的抗性。
J Virol. 1973 Feb;11(2):338-40. doi: 10.1128/JVI.11.2.338-340.1973.
4
New deoxyribonucleic acid polymerase induced by Bacillus subtilis bacteriophage PBS2.枯草芽孢杆菌噬菌体PBS2诱导产生的新型脱氧核糖核酸聚合酶。
J Virol. 1972 Apr;9(4):602-10. doi: 10.1128/JVI.9.4.602-610.1972.
5
Selective replication of bacteriophage phi29 deoxyribonucleic acid in 6-(p-hydroxyphenylazo)-uracil-treated Bacillus subtilis.噬菌体phi29脱氧核糖核酸在6-(对羟基苯偶氮)-尿嘧啶处理的枯草芽孢杆菌中的选择性复制。
J Virol. 1973 Jan;11(1):153-5. doi: 10.1128/JVI.11.1.153-155.1973.
6
Bacillus subtilis bacteriophage PBS2-induced DNA polymerase. Its purification and assay characteristics.枯草芽孢杆菌噬菌体PBS2诱导的DNA聚合酶。其纯化及测定特性。
J Biol Chem. 1978 Dec 10;253(23):8518-25.
7
Involvement of deoxyribonucleic acid polymerase III in W-reactivation in Bacillus subtilis.脱氧核糖核酸聚合酶III参与枯草芽孢杆菌中的W复活作用。
J Bacteriol. 1980 Oct;144(1):473-5. doi: 10.1128/jb.144.1.473-475.1980.
8
Cloning and characterization of the polC region of Bacillus subtilis.枯草芽孢杆菌polC区域的克隆与特性分析
J Bacteriol. 1986 Mar;165(3):951-7. doi: 10.1128/jb.165.3.951-957.1986.
9
Effect of deoxyribonucleic acid replication inhibitors on bacterial recombination.脱氧核糖核酸复制抑制剂对细菌重组的影响。
J Bacteriol. 1976 Apr;126(1):108-21. doi: 10.1128/jb.126.1.108-121.1976.
10
Induction of mutations in B. subtilis phage SPP1 by growth on host cells carrying a mutator DNA polymerase III.通过在携带突变型DNA聚合酶III的宿主细胞上生长诱导枯草芽孢杆菌噬菌体SPP1发生突变。
Mol Gen Genet. 1976 Dec 8;149(2):131-4. doi: 10.1007/BF00332880.

引用本文的文献

1
Diverse functions of restriction-modification systems in addition to cellular defense.限制修饰系统除了具有细胞防御功能外,还有多种功能。
Microbiol Mol Biol Rev. 2013 Mar;77(1):53-72. doi: 10.1128/MMBR.00044-12.
2
Phage phi29 protein p56 prevents viral DNA replication impairment caused by uracil excision activity of uracil-DNA glycosylase.噬菌体φ29蛋白p56可防止由尿嘧啶-DNA糖基化酶的尿嘧啶切除活性导致的病毒DNA复制损伤。
Proc Natl Acad Sci U S A. 2008 Dec 9;105(49):19044-9. doi: 10.1073/pnas.0808797105. Epub 2008 Oct 9.
3
Influence of bacteriophage PBS1 and phi W-14 deoxyribonucleic acids on homologous deoxyribonucleic acid uptake and transformation in competent Bacillus subtilis.噬菌体PBS1和phi W-14脱氧核糖核酸对感受态枯草芽孢杆菌中同源脱氧核糖核酸摄取及转化的影响
J Bacteriol. 1980 Jul;143(1):50-8. doi: 10.1128/jb.143.1.50-58.1980.

本文引用的文献

1
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
2
ENZYMATIC SYNTHESIS OF DEOXYRIBONUCLEIC ACID. XV. PURIFICATION AND PROPERTIES OF A POLYMERASE FROM BACILLUS SUBTILIS.脱氧核糖核酸的酶促合成。十五。枯草芽孢杆菌中一种聚合酶的纯化及性质
J Biol Chem. 1964 Jan;239:259-68.
3
Transducing phages for Bacillus subtilis.用于枯草芽孢杆菌的转导噬菌体。
J Gen Microbiol. 1963 May;31:211-7. doi: 10.1099/00221287-31-2-211.
4
Replacement of thymidylic acid by deoxyuridylic acid in the deoxyribonucleic acid of a transducing phage for Bacillus subtilis.在枯草芽孢杆菌转导噬菌体的脱氧核糖核酸中,胸苷酸被脱氧尿苷酸取代。
Nature. 1963 Feb 23;197:794-5. doi: 10.1038/197794a0.
5
Rifampicin-resistant bacteriophage PBS2 infection and RNA polymerase in Bacillus subtilis.耐利福平噬菌体PBS2感染与枯草芽孢杆菌中的RNA聚合酶
Nucleic Acids Res. 1974 Nov;1(11):1497-502. doi: 10.1093/nar/1.11.1497.
6
Control of DNA synthesis in Bacillus subtilis by phage phi e.噬菌体φe对枯草芽孢杆菌DNA合成的控制
Virology. 1971 Apr;44(1):83-93. doi: 10.1016/0042-6822(71)90155-3.
7
Inhibition of bacterial DNA replication by 6-(p-hydroxyphenylazo)-uracil: differential effect on repair and semi-conservative synthesis in Bacillus subtilis.6-(对羟基苯偶氮)尿嘧啶对细菌DNA复制的抑制作用:对枯草芽孢杆菌修复和半保留合成的不同影响
J Mol Biol. 1971 Jul 14;59(1):1-16. doi: 10.1016/0022-2836(71)90409-8.
8
6-(p-hydroxyphenylazo)-uracil: a selective inhibitor of host DNA replication in phage-infected Bacillus subtilis.6-(对羟基苯偶氮)尿嘧啶:噬菌体感染的枯草芽孢杆菌中宿主DNA复制的选择性抑制剂。
Proc Natl Acad Sci U S A. 1970 Nov;67(3):1454-61. doi: 10.1073/pnas.67.3.1454.
9
Temperature-sensitive mutants of B. subtilis defective in DNA synthesis.枯草芽孢杆菌中DNA合成缺陷的温度敏感突变体。
Cold Spring Harb Symp Quant Biol. 1968;33:307-12. doi: 10.1101/sqb.1968.033.01.034.
10
A novel enzyme, dCTP deaminase, found in Bacillus subtilis infected with phage PBS I.在被噬菌体PBS I感染的枯草芽孢杆菌中发现的一种新型酶——脱氧胞苷三磷酸脱氨酶。
Biochim Biophys Acta. 1969 Mar 18;179(1):18-27. doi: 10.1016/0005-2787(69)90117-8.

枯草芽孢杆菌DNA聚合酶III与噬菌体PBS2诱导的DNA聚合酶的关系以及与含尿嘧啶DNA复制的关系。

Relationship of Bacillus subtilis DNA polymerase III to bacteriophage PBS2-induced DNA polymerase and to the replication of uracil-containing DNA.

作者信息

Hitzeman R A, Price A R

出版信息

J Virol. 1978 Dec;28(3):697-709. doi: 10.1128/JVI.28.3.697-709.1978.

DOI:10.1128/JVI.28.3.697-709.1978
PMID:104052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC525793/
Abstract

In vivo studies of PBS2 phage replication in a temperature-sensitive Bacillus subtilis DNA polymerase III (Pol III) mutant and a temperature-resistant revertant of this mutant have suggested the possible involvement of Pol III in PBS2 DNA synthesis. Previous results with 6-(p-hydroxyphenylazo)-uracil (HPUra), a specific inhibitor of Pol III and DNA replication in uninfected cells, suggest that Pol III is not involved in phage DNA replication, due to its resistance to this drug. Experiments were designed to examine possible explanations for this apparent contradiction. First, assays of the host Pol III and the phage-induced DNA polymerase activities in extracts indicated that a labile Pol III did not result in a labile phage-induced enzyme, suggesting that this new polymerase is not a modified HPUra-resistant form of Pol III. Indeed the purified phage-induced enzyme was resistant to the active, reduced form of HPUra under all assay conditions tested. Since in vitro Pol III was capable of replicating the uracil-containing DNA found in this phage, the sensitivity of the purified enzyme to reduced HPUra was examined using phage DNA as template-primer and dUTP as substrate; these new substrates did not affect the sensitivity of the host enzyme to the drug.

摘要

在对温度敏感的枯草芽孢杆菌DNA聚合酶III(Pol III)突变体及其温度抗性回复突变体中PBS2噬菌体复制的体内研究表明,Pol III可能参与PBS2 DNA合成。先前使用6-(对羟基苯偶氮)尿嘧啶(HPUra)(一种Pol III和未感染细胞中DNA复制的特异性抑制剂)的研究结果表明,由于其对该药物具有抗性,Pol III不参与噬菌体DNA复制。设计实验以检验对这一明显矛盾的可能解释。首先,对提取物中宿主Pol III和噬菌体诱导的DNA聚合酶活性的测定表明,不稳定的Pol III不会导致不稳定的噬菌体诱导酶,这表明这种新的聚合酶不是修饰的抗HPUra形式的Pol III。实际上,在所有测试的测定条件下,纯化的噬菌体诱导酶对活性还原形式的HPUra具有抗性。由于体外Pol III能够复制该噬菌体中含尿嘧啶的DNA,因此使用噬菌体DNA作为模板引物和dUTP作为底物,检测了纯化酶对还原型HPUra的敏感性;这些新底物不影响宿主酶对该药物的敏感性。