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本文引用的文献

1
Chromosome transfer and R-prime plasmid formation mediated by plasmid pULB113 (RP4::mini-Mu) in Alcaligenes eutrophus CH34 and Pseudomonas fluorescens 6.2.由质粒pULB113(RP4::mini-Mu)介导的嗜碱假单胞菌CH34和荧光假单胞菌6.2中的染色体转移和R-prime质粒形成
J Bacteriol. 1983 Sep;155(3):1015-26. doi: 10.1128/jb.155.3.1015-1026.1983.
2
Genetic mapping in Methylophilus methylotrophus AS1.嗜甲基甲基ophilus AS1中的基因图谱
J Gen Microbiol. 1983 Mar;129(3):785-99. doi: 10.1099/00221287-129-3-785.
3
Isolation of an Hfr donor of Pseudomonas aeruginosa PAO by insertion of the plasmid RP1 into the tryptophan synthase gene.通过将质粒RP1插入色氨酸合成酶基因来分离铜绿假单胞菌PAO的高频重组(Hfr)供体。
Mol Gen Genet. 1981;182(2):240-4. doi: 10.1007/BF00269664.
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Physical characterization of mini-mu and mini-D108.微型μ和微型D108的物理特性
Gene. 1981 Jun-Jul;14(1-2):103-13. doi: 10.1016/0378-1119(81)90152-9.
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Genes that control DNA repair and genetic recombination in Escherichia coli.控制大肠杆菌中DNA修复和基因重组的基因。
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Genome organization in Pseudomonas.
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Recalibration of the Pseudomonas aeruginosa strain PAO chromosome map in time units using high-frequency-of-recombination donors.利用高频重组供体对铜绿假单胞菌PAO菌株染色体图谱进行时间单位的重新校准。
Genetics. 1987 Apr;115(4):611-8. doi: 10.1093/genetics/115.4.611.
9
Construction of Hfr-like donors of the obligate methanol-oxidizing bacterium Methylobacillus flagellatum KT.专性甲醇氧化细菌鞭毛甲基杆菌KT的类高频重组(Hfr)供体的构建
FEMS Microbiol Lett. 1989 May;50(1-2):203-6. doi: 10.1016/0378-1097(89)90486-2.
10
Chromosomal genetics of Pseudomonas.假单胞菌的染色体遗传学
Microbiol Rev. 1979 Mar;43(1):73-102. doi: 10.1128/mr.43.1.73-102.1979.

专性甲基营养菌鞭毛甲基杆菌的基因图谱:原质粒的特征及按进入时间单位绘制的染色体图谱

Genetic mapping of the obligate methylotroph Methylobacillus flagellatum: characteristics of prime plasmids and mapping of the chromosome in time-of-entry units.

作者信息

Tsygankov Y D, Kazakova S M, Serebrijski I G

机构信息

Institute of Genetics and Selection of Industrial Microorganisms, Moscow, USSR.

出版信息

J Bacteriol. 1990 May;172(5):2747-54. doi: 10.1128/jb.172.5.2747-2754.1990.

DOI:10.1128/jb.172.5.2747-2754.1990
PMID:2110149
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC208920/
Abstract

A pULB113 (RP4::mini-Mu cts) plasmid was used to generate a library of prime plasmids carrying fragments of the Methylobacillus flagellatum genome. The genes carried by these prime plasmids were identified by complementation after transfer to suitably marked Escherichia coli and Pseudomonas aeruginosa strains. The hybrid plasmids were used for complementation mapping with a range of E. coli, M. flagellatum, and P. aeruginosa mutants. A preliminary map of the M. flagellatum genome section with seven groups of linked markers was obtained. Three of seven groups contain an overlapping sequence of cloned genes and can be considered as one large group of linked genes. A high-frequency-of-recombination donor of M. flagellatum (strain MFK64) mobilized the chromosome in a polarized manner from a single transfer origin. The donor was used to construct a time-of-entry map of the M. flagellatum chromosome. This was achieved by determining the time of entry of six randomly dispersed markers, four of which are included in known groups of linked markers. The linear map of M. flagellatum reported here consists of 44 markers.

摘要

使用携带鞭毛甲基杆菌基因组片段的pULB113(RP4::mini-Mu cts)质粒构建了一个初体质粒文库。将这些初体质粒携带的基因转移到经过适当标记的大肠杆菌和铜绿假单胞菌菌株后,通过互补作用来鉴定。这些杂交质粒用于与一系列大肠杆菌、鞭毛甲基杆菌和铜绿假单胞菌突变体进行互补作图。获得了鞭毛甲基杆菌基因组部分的初步图谱,该图谱有七组连锁标记。七组中的三组包含克隆基因的重叠序列,可被视为一大组连锁基因。鞭毛甲基杆菌的高频重组供体(菌株MFK64)从单个转移起点以极化方式动员染色体。该供体用于构建鞭毛甲基杆菌染色体的进入时间图谱。这是通过确定六个随机分散标记的进入时间来实现的,其中四个标记包含在已知的连锁标记组中。这里报道的鞭毛甲基杆菌线性图谱由44个标记组成。