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微菌素B17,一种制备最大细胞的新型工具:IncFII微型复制子pMccB17编码的多肽的鉴定。

Microcin B17, a novel tool for preparation of maxicells: identification of polypeptides encoded by the IncFII minireplicon pMccB17.

作者信息

Mayo O, Hernández-Chico C, Moreno F

机构信息

Unidad de Genética Molecular, Servicio de Microbiología, Hospital Ramón y Cajal, Madrid, Spain.

出版信息

J Bacteriol. 1988 May;170(5):2414-7. doi: 10.1128/jb.170.5.2414-2417.1988.

DOI:10.1128/jb.170.5.2414-2417.1988
PMID:3283111
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC211143/
Abstract

The DNA replication inhibitor peptide microcin B17 is shown to be a useful tool for preparing Escherichia coli maxicells. To illustrate its usefulness, we have identified polypeptides synthesized from pMccB17 and R100 IncFII miniplasmids. After comparing the respective polypeptides and the miniplasmid restriction maps, we concluded that these plasmids share extensive homology in the basic replicon but are different for an adjacent region (parD) that is involved in plasmid stability and maintenance.

摘要

DNA复制抑制剂小菌素B17被证明是制备大肠杆菌最大细胞的有用工具。为了说明其有用性,我们鉴定了从pMccB17和R100 IncFII微型质粒合成的多肽。在比较了各自的多肽和微型质粒限制图谱后,我们得出结论,这些质粒在基本复制子中具有广泛的同源性,但在与质粒稳定性和维持有关的相邻区域(parD)有所不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6ed/211143/b5742ad3a048/jbacter00183-0421-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6ed/211143/b5742ad3a048/jbacter00183-0421-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6ed/211143/b5742ad3a048/jbacter00183-0421-a.jpg

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Microcin B17, a novel tool for preparation of maxicells: identification of polypeptides encoded by the IncFII minireplicon pMccB17.微菌素B17,一种制备最大细胞的新型工具:IncFII微型复制子pMccB17编码的多肽的鉴定。
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本文引用的文献

1
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Mol Gen Genet. 1981;184(1):56-61. doi: 10.1007/BF00271195.
2
Genes and sites involved in replication and incompatibility of an R100 plasmid derivative based on nucleotide sequence analysis.基于核苷酸序列分析的R100质粒衍生物复制与不相容性相关的基因和位点
Mol Gen Genet. 1980;179(3):527-37. doi: 10.1007/BF00271742.
3
Analysis of plasmid genome evolution based on nucleotide-sequence comparison of two related plasmids of Escherichia coli.
appR基因产物激活微菌素C7质粒基因的转录。
J Bacteriol. 1989 May;171(5):2906-8. doi: 10.1128/jb.171.5.2906-2908.1989.
4
The peptide antibiotic microcin B17 induces double-strand cleavage of DNA mediated by E. coli DNA gyrase.肽抗生素微菌素B17可诱导由大肠杆菌DNA促旋酶介导的DNA双链断裂。
EMBO J. 1991 Feb;10(2):467-76. doi: 10.1002/j.1460-2075.1991.tb07969.x.
基于大肠杆菌两个相关质粒核苷酸序列比较的质粒基因组进化分析。
Gene. 1982 Mar;17(3):299-310. doi: 10.1016/0378-1119(82)90146-9.
4
The nucleotide sequence of the replication control region of the resistance plasmid R1drd-19.抗性质粒R1drd - 19复制控制区的核苷酸序列。
Mol Gen Genet. 1981;181(1):116-22. doi: 10.1007/BF00339014.
5
Cleavage of structural proteins during the assembly of the head of bacteriophage T4.在噬菌体T4头部组装过程中结构蛋白的切割
Nature. 1970 Aug 15;227(5259):680-5. doi: 10.1038/227680a0.
6
The DNA replication inhibitor microcin B17 is a forty-three-amino-acid protein containing sixty percent glycine.DNA复制抑制剂小菌素B17是一种含有60%甘氨酸的43个氨基酸的蛋白质。
Proteins. 1986 Nov;1(3):230-8. doi: 10.1002/prot.340010305.
7
Identification of components of a new stability system of plasmid R1, ParD, that is close to the origin of replication of this plasmid.鉴定质粒R1新稳定性系统ParD的组成部分,该系统靠近此质粒的复制起点。
Mol Gen Genet. 1987 Nov;210(1):101-10. doi: 10.1007/BF00337764.
8
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9
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