Cloning and sequence analysis of a plasmid replicon from Lactococcus lactis subsp. cremoris FG2

被引:8
|
作者
Liu, CQ [1 ]
Duan, KM [1 ]
Dunn, NW [1 ]
机构
[1] UNIV NEW S WALES, DEPT BIOTECHNOL, COOPERAT RES CTR FOOD IND INNOVAT, SYDNEY, NSW 2052, AUSTRALIA
来源
关键词
Lactococcus lactis; plasmid replicon;
D O I
10.2323/jgam.43.75
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A replication region from one of the Lactococcus lactis subsp, cremoris FG2 plasmids was isolated by cloning of a 4.8-kb Xbal fragment into a replication probe vector and transformation into L. lactis LM0230. A 1.8-kb region within this fragment was sequenced and confirmed by PCR subcloning to encode a functional replicon in LM0230. The replicon consists of an open reading frame encoding a putative replication protein (Rep) of 386 amino acids and a non-coding region (ori) which features several structural motifs typical of other known replication origins, including a 22-bp iteron sequence tandemly repeated three and a half times, a 10-bp direct repeat and two sets of inverted repeats. The ori region could drive replication of its plasmid when supplied with the replication region in-trans. The lack of detectable single-stranded DNA during replication and the existence of extensive homology with other known lactococcal theta replicons strongly suggest that this region encodes a theta-replicating mechanism.
引用
收藏
页码:75 / 80
页数:6
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