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温度和宿主细胞遗传特性对含脂质噬菌体PR4在大肠杆菌中复制的影响。

Effects of temperature and host cell genetic characteristics on the replication of the lipid-containing bacteriophage PR4 in Escherichia coli.

作者信息

Sands J A, Auperin D

出版信息

J Virol. 1977 May;22(2):315-20. doi: 10.1128/JVI.22.2.315-320.1977.

DOI:10.1128/JVI.22.2.315-320.1977
PMID:325229
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC515721/
Abstract

The lipid-containing bacteriophage PR4 is of special intest because it can replicate in various gram-negative bacteria, including Escherichia coli, that carry one of a group of drug resistance plasmids. PR4 grown in E. coli strain PS2R contains about 10% lipid by weight, with the negatively charged phospholipid phosphatidylglycerol being the most abundant lipid in the virion. We now report the following. (i) PR4 attaches to E. coli with an attachment rate constant of Ka approximately 6.2 X 10(-10) ml/min, which is about twice that of the enveloped phage phi6 (to Pseudomonas phaseolicola), but a factor of 5 less than that of phage PM2 (to Pseudomonas BAL-31). (ii) Use of an E. coli glycerol auxotroph indicated that a normal amount of PR4 replication occurs only if glycerol starvation (inhibition of all phospholipid synthesis) begins no earlier than about halfway through the lytic cycle. (iii) Use of an E. coli fatty acid synthesis temperature-sensitive mutant and an E. coli phosphatidylethanolamine synthesis temperature-sensitive mutant indicate that PR4 replication can occur in the absence of either normal fatty acid synthesis or normal phospholipid synthesis if the infection takes place prior to the termination of overall cell growth and the onset of cell death, (iv) Whereas PR4 burst size in nutrient media at 30 degrees C to 42%C is about 40, the burst size at 20 degrees C is less than 3, Temperature-shift experiments show that the temperature late in infection determines the burst size.

摘要

含脂质的噬菌体PR4特别有趣,因为它能在各种革兰氏阴性细菌中复制,包括携带一组耐药质粒之一的大肠杆菌。在大肠杆菌菌株PS2R中生长的PR4按重量计含有约10%的脂质,带负电荷的磷脂磷脂酰甘油是病毒体中最丰富的脂质。我们现在报告以下内容。(i)PR4以约Ka为6.2×10(-10)ml/分钟的附着速率常数附着于大肠杆菌,这约为包膜噬菌体phi6(对菜豆假单胞菌)的两倍,但比噬菌体PM2(对假单胞菌BAL-31)低5倍。(ii)使用大肠杆菌甘油营养缺陷型表明,只有当甘油饥饿(所有磷脂合成的抑制)不早于裂解周期大约一半时开始,PR4才会发生正常量的复制。(iii)使用大肠杆菌脂肪酸合成温度敏感突变体和大肠杆菌磷脂酰乙醇胺合成温度敏感突变体表明,如果感染发生在细胞总体生长终止和细胞死亡开始之前,PR4可以在没有正常脂肪酸合成或正常磷脂合成的情况下发生复制,(iv)虽然PR4在30℃至42℃的营养培养基中的裂解量约为40,但在20℃时的裂解量小于3。温度转换实验表明,感染后期的温度决定了裂解量。

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1
Effects of temperature and host cell genetic characteristics on the replication of the lipid-containing bacteriophage PR4 in Escherichia coli.温度和宿主细胞遗传特性对含脂质噬菌体PR4在大肠杆菌中复制的影响。
J Virol. 1977 May;22(2):315-20. doi: 10.1128/JVI.22.2.315-320.1977.
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J Virol. 1976 Aug;19(2):296-301. doi: 10.1128/JVI.19.2.296-301.1976.
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Inhibitory effect of fatty acids on the entry of the lipid-containing bacteriophage PR4 into Escherichia coli.脂肪酸对含脂噬菌体PR4进入大肠杆菌的抑制作用。
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Enrichment of the bacteriophage PR4 membrane in phosphatidylglycerol is not essential for phage assembly and infectivity.噬菌体PR4膜中磷脂酰甘油的富集对于噬菌体组装和感染性并非必不可少。
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Lipid-containing bacteriophage PR4: structure and life cycle.含脂质噬菌体PR4:结构与生命周期
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引用本文的文献

1
Inhibition of entry of the lipid-containing bacteriophage PR4 by fatty acid derivatives.脂肪酸衍生物对含脂质噬菌体PR4进入的抑制作用。
J Virol. 1979 Jan;29(1):413-6. doi: 10.1128/JVI.29.1.413-416.1979.
2
Enzymology, genetics, and regulation of membrane phospholipid synthesis in Escherichia coli.大肠杆菌中膜磷脂合成的酶学、遗传学及调控
Microbiol Rev. 1978 Sep;42(3):614-59. doi: 10.1128/mr.42.3.614-659.1978.
3
Inhibitory effect of fatty acids on the entry of the lipid-containing bacteriophage PR4 into Escherichia coli.脂肪酸对含脂噬菌体PR4进入大肠杆菌的抑制作用。
J Virol. 1978 Feb;25(2):479-85. doi: 10.1128/JVI.25.2.479-485.1978.

本文引用的文献

1
Bacteriophage phi6: a Lipid-Containing Virus of Pseudomonas phaseolicola.噬菌体phi6:一种含脂质的菜豆假单胞菌病毒。
J Virol. 1973 May;11(5):799-805. doi: 10.1128/JVI.11.5.799-805.1973.
2
Calcium requirement for assemby of the lipid-containing bacteriophage PM2.含脂质噬菌体PM2组装所需的钙
Biochim Biophys Acta. 1974 Mar 29;339(3):311-22. doi: 10.1016/0005-2736(74)90158-8.
3
Structure and synthesis of a lipid-containing bacteriophage. 13. Studies on the origin of the viral phospholipids.一种含脂质噬菌体的结构与合成。13. 病毒磷脂起源的研究。
Virology. 1974 Jun;59(2):408-17.
4
Temperature-sensitive mutants of Escherichia coli requiring saturated and unsaturated fatty acids for growth: isolation and properties.大肠杆菌的温度敏感突变体,生长需要饱和脂肪酸和不饱和脂肪酸:分离与特性
Proc Natl Acad Sci U S A. 1972 Nov;69(11):3105-9. doi: 10.1073/pnas.69.11.3105.
5
Control of phospholipid synthesis and viral assembly by bacteriophage PM2.噬菌体PM2对磷脂合成和病毒组装的控制
Biochim Biophys Acta. 1974 Sep 23;363(3):340-50. doi: 10.1016/0005-2736(74)90073-x.
6
Temperature sensitivity of the assembly process of the enveloped bacteriophage phi6.包膜噬菌体phi6组装过程的温度敏感性
Biochim Biophys Acta. 1974 Dec 10;373(2):277-85. doi: 10.1016/0005-2736(74)90151-5.
7
Lateral phase separations in Escherichia coli membranes.大肠杆菌膜中的侧向相分离。
Biochim Biophys Acta. 1974 Apr 29;345(2):220-30. doi: 10.1016/0005-2736(74)90260-0.
8
Temporal origin of viral phospholipids of the enveloped bacteriophage phi 6.包膜噬菌体phi 6病毒磷脂的时间起源
Can J Microbiol. 1976 Feb;22(2):154-8. doi: 10.1139/m76-021.
9
Host membrane lipid synthesis is not required for successful phage T4 infection.噬菌体T4成功感染并不需要宿主细胞膜脂质合成。
Virology. 1976 Jan;69(1):332-5. doi: 10.1016/0042-6822(76)90221-x.
10
Thermal regulation of the membrane lipid composition of Escherichia coli. Evidence for the direct control of fatty acid synthesis.大肠杆菌膜脂质组成的热调节。脂肪酸合成直接调控的证据。
J Biol Chem. 1975 Sep 10;250(17):7074-7.