Two novel conjugative plasmids from a single strain of Sulfolobus

被引:24
作者
Erauso, Gael [1 ]
Stedman, Kenneth M.
van de Werken, Harmen J. G.
Zillig, Wolfram
van der Oost, John
机构
[1] Wageningen Univ, Microbiol Lab, Wageningen, Netherlands
[2] Univ Bretagne Occidentale, IUEM, CNRS, UMR 6539, F-29280 Plouzane, France
[3] Max Planck Inst Biochem, D-82152 Martinsried, Germany
[4] Portland State Univ, Dept Biol, Portland, OR 97207 USA
来源
MICROBIOLOGY-SGM | 2006年 / 152卷
关键词
D O I
10.1099/mic.0.28861-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Two conjugative plasmids (CPs) were isolated and characterized from the same 'Sulfolobus islandicus' strain, SOG2/4, The plasmids were separated from each other and transferred into Sulfolobus soltataricus. One has a high copy number and is not stable (pSOG1) whereas the other has a low copy number and is stably maintained (pSOG2). Plasmid pSOG2 is the first Sulfolobus CP found to have these characteristics. The genomes of both pSOG plasmids have been sequenced and were compared to each other and the available Sulfolobus CPs. Interestingly, apart from a very well-conserved core, 70% of the pSOG 1 and pSOG2 genomes is largely different and composed of a mixture of genes that often resemble counterparts in previously described Sulfolobus CPs. However, about 20% of the predicted genes do not have known homologues, not even in other CPs. Unlike pSOG1, pSOG2 does not contain a gene for the highly conserved PIrA protein nor for obvious homologues of partitioning proteins. Unlike pNOB8 and pKEF9, both pSOG plasmids lack the so-called clustered regularly interspaced short palindrome repeats (CRISPRs). The sites of recombination between the two genomes can be explained by the presence of recombination motifs previously identified in other Sulfolobus CPs. Like other Sulfolobus CPs, the pSOG plasmids possess a gene encoding an integrase of the tyrosine recombinase family. This integrase probably mediates plasmid site-specific integration into the host chromosome at the highly conserved tRNA(Glu) loci.
引用
收藏
页码:1951 / 1968
页数:18
相关论文
共 92 条
[1]   Production of recombinant and tagged proteins in the hyperthermophilic archaeon Sulfolobus solfataricus [J].
Albers, SV ;
Jonuscheit, M ;
Dinkelaker, S ;
Urich, T ;
Kletzin, A ;
Tampé, R ;
Driessen, AJM ;
Schleper, C .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2006, 72 (01) :102-111
[2]   Shuttle vectors for hyperthermophilic archaea [J].
Aravalli, RN ;
Garrett, RA .
EXTREMOPHILES, 1997, 1 (04) :183-191
[3]   The many faces of the helix-turn-helix domain: Transcription regulation and beyond [J].
Aravind, L ;
Anantharaman, V ;
Balaji, S ;
Babu, MM ;
Iyer, LM .
FEMS MICROBIOLOGY REVIEWS, 2005, 29 (02) :231-262
[4]   DNA-binding proteins and evolution of transcription regulation in the archaea [J].
Aravind, L ;
Koonin, EV .
NUCLEIC ACIDS RESEARCH, 1999, 27 (23) :4658-4670
[5]   The genetic element pSSVx of the extremely thermophilic crenarchaeon Sulfolobus is a hybrid between a plasmid and a virus [J].
Arnold, HP ;
She, Q ;
Phan, H ;
Stedman, K ;
Prangishvili, D ;
Holz, I ;
Kristjansson, JK ;
Garrett, R ;
Zillig, W .
MOLECULAR MICROBIOLOGY, 1999, 34 (02) :217-226
[6]   Characterization and functional complementation of a nonlethal deletion in the chromosome of a β-glycosidase mutant of Sulfolobus solfataricus [J].
Bartolucci, S ;
Rossi, M ;
Cannio, R .
JOURNAL OF BACTERIOLOGY, 2003, 185 (13) :3948-3957
[7]   The role of transcription factor B in transcription initiation and promoter clearance in the archaeon Sulfolobus acidocaldarius [J].
Bell, SD ;
Jackson, SP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (17) :12934-12940
[8]   M13 AND PUC VECTORS WITH NEW UNIQUE RESTRICTION SITES FOR CLONING [J].
BENES, V ;
HOSTOMSKY, Z ;
ARNOLD, L ;
PACES, V .
GENE, 1993, 130 (01) :151-152
[9]   The bacterial ParA-ParB partitioning proteins [J].
Bignell, C ;
Thomas, CM .
JOURNAL OF BIOTECHNOLOGY, 2001, 91 (01) :1-34
[10]  
BIRBOIM HC, 1979, NUCLEIC ACIDS RES, V7, P1513