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DNA 回旋酶抑制剂对大肠杆菌多胺营养缺陷型菌株的影响。

Effects of DNA gyrase inhibitors in a polyamine-auxotrophic strain of Escherichia coli.

作者信息

Duschak V G, Goldemberg S H

机构信息

Instituto de Investigaciones Bioquimicas Fundacion Campomar, Buenos Aires, Argentina.

出版信息

Biochim Biophys Acta. 1987 Oct 9;910(1):21-6. doi: 10.1016/0167-4781(87)90090-x.

DOI:10.1016/0167-4781(87)90090-x
PMID:2820496
Abstract

The polyamine content of the Escherichia coli polyamine-auxotrophic strain BGA 8 seemed to influence the effects of nalidixic acid, an antibiotic acting on subunit A of DNA gyrase. The growth rate was more affected under conditions of putrescine depletion and the inhibition could be partially relieved if the polycation was added back to the culture. DNA synthesis was likewise more sensitive to nalidixic acid in cultures grown without polyamine. The expression of some proteins characteristic of the heat-shock response, evoked by the antibiotic, showed a different persistence according to the presence or absence of polyamines. Novobiocin, acting on subunit B of gyrase, also promoted a differential effect depending on the polyamine content, but in this case putrescine-supplemented cells were more sensitive. The described findings suggest a role of polyamines in all the reactions carried out by gyrase, perhaps due to the influence of the polycations on the state of DNA aggregation.

摘要

大肠杆菌多胺营养缺陷型菌株BGA 8的多胺含量似乎会影响萘啶酸的作用效果,萘啶酸是一种作用于DNA促旋酶A亚基的抗生素。在腐胺耗尽的条件下,生长速率受到的影响更大,如果将这种聚阳离子重新添加到培养物中,抑制作用可部分缓解。在没有多胺的情况下培养的细菌中,DNA合成对萘啶酸同样更敏感。由抗生素引发的一些热休克反应特征性蛋白质的表达,根据多胺的存在与否表现出不同的持续性。新霉素作用于促旋酶的B亚基,也会根据多胺含量产生不同的影响,但在这种情况下,补充腐胺的细胞更敏感。上述研究结果表明,多胺在促旋酶进行的所有反应中都发挥作用,这可能是由于聚阳离子对DNA聚集状态的影响。

相似文献

1
Effects of DNA gyrase inhibitors in a polyamine-auxotrophic strain of Escherichia coli.DNA 回旋酶抑制剂对大肠杆菌多胺营养缺陷型菌株的影响。
Biochim Biophys Acta. 1987 Oct 9;910(1):21-6. doi: 10.1016/0167-4781(87)90090-x.
2
Increase in synthesis and stability of sigma 32 on treatment with inhibitors of DNA gyrase in Escherichia coli.在大肠杆菌中用DNA回旋酶抑制剂处理后,σ32的合成和稳定性增加。
Mol Gen Genet. 1996 Dec 13;253(3):297-302. doi: 10.1007/pl00008596.
3
Transient DNA relaxation in Escherichia coli induced by nalidixic acid.萘啶酸诱导大肠杆菌中的瞬时DNA松弛
Biol Pharm Bull. 1997 May;20(5):467-70. doi: 10.1248/bpb.20.467.
4
Effect of the bacterial DNA gyrase inhibitors, novobiocin, nalidixic acid, and oxolinic acid, on oxidative phosphorylation.细菌DNA促旋酶抑制剂新生霉素、萘啶酸和恶喹酸对氧化磷酸化的影响。
J Biol Chem. 1986 Jul 5;261(19):8604-7.
5
Nalidixic acid resistance: a second genetic character involved in DNA gyrase activity.萘啶酸抗性:参与DNA回旋酶活性的第二个遗传特征。
Proc Natl Acad Sci U S A. 1977 Nov;74(11):4772-6. doi: 10.1073/pnas.74.11.4772.
6
Mechanism of action of nalidixic acid: purification of Escherichia coli nalA gene product and its relationship to DNA gyrase and a novel nicking-closing enzyme.萘啶酸的作用机制:大肠杆菌nalA基因产物的纯化及其与DNA回旋酶和一种新型切口封闭酶的关系。
Proc Natl Acad Sci U S A. 1977 Nov;74(11):4767-71. doi: 10.1073/pnas.74.11.4767.
7
Novobiocin inhibits Xenopus transcription factor IIIA-DNA interactions.新生霉素抑制非洲爪蟾转录因子IIIA与DNA的相互作用。
J Biol Chem. 1987 Sep 5;262(25):11916-9.
8
Identification of DNA topoisomerases involved in immediate and transient DNA relaxation induced by heat shock in Escherichia coli.大肠杆菌中参与热休克诱导的即时和短暂DNA松弛的DNA拓扑异构酶的鉴定。
Mol Gen Genet. 1994 Sep 1;244(5):451-5. doi: 10.1007/BF00583895.
9
Positively supercoiled plasmid DNA is produced by treatment of Escherichia coli with DNA gyrase inhibitors.通过用DNA回旋酶抑制剂处理大肠杆菌可产生正超螺旋质粒DNA。
Nucleic Acids Res. 1983 May 25;11(10):2999-3017. doi: 10.1093/nar/11.10.2999.
10
The effect of bacterial DNA gyrase inhibitors on DNA synthesis in mammalian mitochondria.细菌DNA促旋酶抑制剂对哺乳动物线粒体中DNA合成的影响。
Biochim Biophys Acta. 1983 Sep 9;740(4):417-27. doi: 10.1016/0167-4781(83)90090-8.

引用本文的文献

1
Polyamine--DNA nexus: structural ramifications and biological implications.多胺 - DNA 关系:结构影响及生物学意义
Mol Cell Biochem. 1991 Feb 2;100(2):129-40. doi: 10.1007/BF00234162.
2
Possible prebiotic significance of polyamines in the condensation, protection, encapsulation, and biological properties of DNA.多胺在DNA的缩合、保护、封装及生物学特性方面可能具有的益生元意义。
Orig Life Evol Biosph. 1991;21(4):225-42. doi: 10.1007/BF01809858.