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产细菌素质粒Clo DF13复制突变体的分离与鉴定

Isolation and characterization of a copy mutant of the bacteriocinogenic plasmid Clo DF13.

作者信息

Kool A J, Nijkamp H J

出版信息

J Bacteriol. 1974 Nov;120(2):569-78. doi: 10.1128/jb.120.2.569-578.1974.

Abstract

After nitrosoguanidine mutagenesis, strain Escherichia coli P678-54, bacteriocinogenic for Clo DF13, yielded a mutant strain that showed an enhanced bacteriocin production. The results from conjugation experiments indicated that the mutation, responsible for the enhanced bacteriocin production, is located on the Clo DF13 plasmid. The following properties of strains harboring the mutant Clo DF13 plasmid could be observed. (i) The bacteriocin production in these strains can be further enhanced at least fourfold by mitomycin C. (ii) The fraction of spontaneously induced cells, as revealed by lacunae experiments, in cultures of these strains is about nine times higher than in cultures of wild-type Clo DF13-harboring strains. (iii) Chromosomeless minicells from strain P678-54 harboring the mutant Clo DF13 plasmid synthesize about six times more deoxyribonucleic acid, ribonucleic acid, and protein as compared to wild-type Clo DF13-harboring minicells. (iv) Analysis of this mutant Clo DF13-specific ribonucleic acid and protein on polyacrylamide gels revealed mainly the same ribonucleic acid and polypeptide species as synthesized by the wild-type Clo DF13 minicells, but in larger amounts (Kool et al., 1974). (v) Segregation experiments, using a strain with temperature-sensitive polymerase I, show that mutant Clo DF13-harboring cells contain an average of 70 Clo DF13 copies per cell, whereas wild-type Clo DF13-harboring cells contain only about 10 Clo DF13 copies per cell. The data presented in this paper indicate that the mutation on the Clo DF13 plasmid leads to an altered control of Clo DF13 replication and results in an enhanced number of Clo DF13 copies per cell. As a secondary effect, this enhanced number of Clo DF13 copies enhances the probability of "spontaneous" induction per cell. Since the mutation is plasmid specific and affects the number of plasmid copies produced, one can conclude that the Clo DF13 plasmid is not dependent solely on chromosomal information, but that at least plasmid base sequences are involved in Clo DF13 plasmid replication.

摘要

经亚硝基胍诱变后,对Clo DF13具有产细菌素能力的大肠杆菌P678 - 54菌株产生了一种细菌素产量提高的突变菌株。接合实验结果表明,导致细菌素产量提高的突变位于Clo DF13质粒上。可以观察到携带突变型Clo DF13质粒的菌株具有以下特性。(i) 这些菌株中的细菌素产量可通过丝裂霉素C进一步提高至少四倍。(ii) 如空白实验所揭示的,这些菌株培养物中自发诱导细胞的比例比携带野生型Clo DF13的菌株培养物中的高约九倍。(iii) 携带突变型Clo DF13质粒的P678 - 54菌株的无染色体微小细胞合成的脱氧核糖核酸、核糖核酸和蛋白质比携带野生型Clo DF13的微小细胞多约六倍。(iv) 在聚丙烯酰胺凝胶上对这种突变型Clo DF13特异性核糖核酸和蛋白质的分析表明,其主要合成的核糖核酸和多肽种类与野生型Clo DF13微小细胞相同,但数量更多(库尔等人,1974年)。(v) 使用具有温度敏感性聚合酶I的菌株进行的分离实验表明,携带突变型Clo DF13的细胞平均每个细胞含有70个Clo DF13拷贝,而携带野生型Clo DF13的细胞每个细胞仅含有约10个Clo DF13拷贝。本文提供的数据表明,Clo DF13质粒上的突变导致Clo DF13复制的控制改变,并导致每个细胞中Clo DF13拷贝数增加。作为次要效应,这种增加的Clo DF13拷贝数增加了每个细胞“自发”诱导的概率。由于该突变是质粒特异性的,并影响产生的质粒拷贝数,因此可以得出结论,Clo DF13质粒并非仅依赖于染色体信息,而是至少质粒碱基序列参与了Clo DF13质粒的复制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/394a/245813/34cdb3051665/jbacter00335-0020-a.jpg

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