Nucleotide sequence of the cryptic plasmid pTT8 from Thermus thermophilus HB8 and isolation and characterization of its high-copy-number mutant

被引:17
|
作者
Takayama, G
Kosuge, T
Maseda, H
Nakamura, A
Hoshino, T [1 ]
机构
[1] Univ Tsukuba, Inst Appl Biochem, Tsukuba, Ibaraki 3058572, Japan
[2] Natl Inst Genet, Ctr Informat Biol, Mishima, Shizuoka 4118540, Japan
[3] Natl Inst Genet, DNA Data Bank Japan, Mishima, Shizuoka 4118540, Japan
关键词
Thermus thermophilus; cryptic plasmid; high-copy-number mutant; expression vector;
D O I
10.1016/j.plasmid.2004.01.003
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The complete nucleotide sequence of pTT8, a cryptic plasmid from Thermus thermophilus HB8, was determined. pTT8 was 9328 bp long and its G + C content was 69%. pTT8 contained eight putative open reading frames, three of which showed extensive similarities to the plasmid addiction proteins PasA and PasB of pTC-F14 and pAM10.6, and the RepA protein of the ColE2-related plasmids, respectively. During the analysis of pTT8-based plasmid pPP442, which had been obtained during a promoter-screening experiment, we occasionally isolated a plasmid with a relatively high-copy-number. This plasmid, pPP442m, contained a 1025 bp fragment derived from the genome of the HB27 host strain immediately upstream of the putative repA gene. Using the ori region of pPP442m, we constructed an expression vector, pTEV131m, with an estimated high-copy-number of 30-40. This plasmid was stably maintained in T thermophilus HB27 under nonselective conditions for at least 100 generations. Cloning of the alpha-amylase gene of Bacillus stearothermophilus DY-5 into pTEV131m gave more than twofold production of the enzyme compared with pTEV131, the parental plasmid. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:227 / 237
页数:11
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