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链霉菌属中噬菌体噬菌斑形成的限制

Restriction of bacteriophage plaque formation in Streptomyces spp.

作者信息

Cox K L, Baltz R H

出版信息

J Bacteriol. 1984 Aug;159(2):499-504. doi: 10.1128/jb.159.2.499-504.1984.

DOI:10.1128/jb.159.2.499-504.1984
PMID:6086574
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC215672/
Abstract

Several Streptomyces species that produce restriction endonucleases were characterized for their ability to propagate 10 different broad host range bacteriophages. Each species displayed a different pattern of plaque formation. A restrictionless mutant of S. albus G allowed plaque formation by all 10 phages, whereas the wild-type strain showed plaques with only 2 phages. DNA isolated from three of the phages was analyzed for the presence of restriction sites for Streptomyces species-encoded enzymes, and a very strong correlation was established between the failure to form plaques on Streptomyces species that produced particular restriction enzymes and the presence of the corresponding restriction sites in the phage DNA. Also, the phages that lacked restriction sites in their DNA generally formed plaques on the corresponding restriction endonuclease-producing hosts at high efficiency. The DNAs from the three phages analyzed also generally contained either many or no restriction sites for the Streptomyces species-produced enzymes, suggesting a strong evolutionary trend to either eliminate all or tolerate many restriction sites. The data indicate that restriction plays a major role in host range determination for Streptomyces phages. Analysis of bacteriophage host ranges of many other uncharacterized Streptomyces hosts has identified four relatively nonrestricting hosts, at least two of which may be suitable hosts for gene cloning. The data also suggest that several restriction systems remain to be identified in the genus Streptomyces.

摘要

对几种产生限制性内切核酸酶的链霉菌进行了特性分析,以研究它们传播10种不同的广宿主范围噬菌体的能力。每个菌种都表现出不同的噬菌斑形成模式。白色链霉菌G的一个无限制突变体允许所有10种噬菌体形成噬菌斑,而野生型菌株仅对2种噬菌体形成噬菌斑。对从其中3种噬菌体中分离的DNA进行分析,以检测链霉菌属编码酶的限制位点的存在情况,并且在不能在产生特定限制酶的链霉菌上形成噬菌斑与噬菌体DNA中相应限制位点的存在之间建立了非常强的相关性。此外,DNA中缺乏限制位点的噬菌体通常能高效地在相应的产生限制性内切核酸酶的宿主上形成噬菌斑。所分析 的3种噬菌体的DNA通常也要么含有许多链霉菌属产生的酶的限制位点,要么不含限制位点,这表明存在一种强烈的进化趋势,即要么消除所有限制位点,要么耐受许多限制位点。数据表明,限制作用在链霉菌噬菌体的宿主范围确定中起主要作用。对许多其他未鉴定的链霉菌宿主的噬菌体宿主范围进行分析,已鉴定出4种相对非限制性的宿主,其中至少有两种可能是适合基因克隆的宿主。数据还表明,在链霉菌属中仍有几种限制系统有待鉴定。

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本文引用的文献

1
A DNA cloning system for interspecies gene transfer in antibiotic-producing Streptomyces.一种用于抗生素产生菌链霉菌种间基因转移的DNA克隆系统。
Nature. 1980 Apr 10;284(5756):526-31. doi: 10.1038/284526a0.
2
Protoplast fusion in Streptomyces: conditions for efficient genetic recombination and cell regeneration.链霉菌中的原生质体融合:高效基因重组和细胞再生的条件
J Gen Microbiol. 1981 Nov;127(1):137-46. doi: 10.1099/00221287-127-1-137.
3
Properties of S-adenosyl-L-methionine:macrocin O-methyltransferase in extracts of Streptomyces fradiae strains which produce normal or elevated levels of tylosin and in mutants blocked in specific O-methylations.弗氏链霉菌菌株提取物中S-腺苷-L-甲硫氨酸:大环菌素O-甲基转移酶的特性,这些菌株产生正常或高水平的泰乐菌素,以及在特定O-甲基化中受阻的突变体。
Antimicrob Agents Chemother. 1981 Sep;20(3):370-7. doi: 10.1128/AAC.20.3.370.
4
Physico-chemical properties of new acyl derivatives of tylosin produced by microbial transformation.
J Antibiot (Tokyo). 1980 Nov;33(11):1300-8. doi: 10.7164/antibiotics.33.1300.
5
A new temperate phage of streptomyces venezuelae: morphology, DNA molecular weight and host range of SV2.委内瑞拉链霉菌的一种新温和噬菌体:SV2的形态、DNA分子量及宿主范围
Can J Microbiol. 1981 May;27(5):496-9. doi: 10.1139/m81-073.
6
Cloning and expression in streptomyces lividans of antibiotic resistance genes derived from Escherichia coli.源自大肠杆菌的抗生素抗性基因在变铅青链霉菌中的克隆与表达。
J Bacteriol. 1981 Apr;146(1):360-8. doi: 10.1128/jb.146.1.360-368.1981.
7
Genetics and biochemistry on tylosin production: a model for genetic engineering in antibiotic-producing Streptomyces.泰乐菌素生产的遗传学与生物化学:抗生素生产链霉菌基因工程的一个模型
Basic Life Sci. 1982;19:431-44. doi: 10.1007/978-1-4684-4142-0_32.
8
Advances in protoplast fusion and transformation in Streptomyces.链霉菌原生质体融合与转化的研究进展
Experientia Suppl. 1983;46:143-8. doi: 10.1007/978-3-0348-6776-4_18.
9
Uses of recombinant DNA for analyses of Streptomyces species.
Ann N Y Acad Sci. 1983;413:31-46. doi: 10.1111/j.1749-6632.1983.tb47876.x.
10
Development of cloning vehicles from the Streptomyces plasmid pFJ103.基于链霉菌质粒pFJ103构建克隆载体
Gene. 1982 Dec;20(3):451-7. doi: 10.1016/0378-1119(82)90214-1.