CLONING OF FRANKIA SPECIES PUTATIVE TRNA(PRO) GENES AND THEIR EFFICACY FOR PSAM2 SITE-SPECIFIC INTEGRATION IN STREPTOMYCES-LIVIDANS

被引:10
作者
ALEGRE, MT
COURNOYER, B
MESAS, JM
GUERINEAU, M
NORMAND, P
PERNODET, JL
机构
[1] POLITECN SUPER,E-27002 LUGO,SPAIN
[2] UNIV LYON 1,MICROBIOL SOLS LAB,CNRS,URA 1450,F-69622 VILLEURBANNE,FRANCE
[3] UNIV PARIS 11,INST GENET & MICROBIOL,CNRS,URA 1354,F-91405 ORSAY,FRANCE
关键词
D O I
10.1128/AEM.60.12.4279-4283.1994
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
pSAM2 is a conjugative Streptomyces ambofaciens mobile genetic element that can transfer and integrate site specifically in the genome. The chromosomal attachment site (attB) for pSAM2 site-specific recombination for two Frankia species was analyzed. It overlaps putative proline tRNA genes having a 3'-terminal CCA sequence, an uncommon feature among actinomycetes. pSAM2 is able to integrate into a cloned Frankia attB site harbored in Streptomyces lividans. The integration event removes the 3'-terminal CCA sequence and introduces a single nucleotide difference in the T Psi C loop of the putative Frankia tRNA(pro) gene. Major differences between the attP sequence from pSAM2 and the Frankia attB sequence restrict the identity segment to a 43-bp-long region. Only one mismatch is found between these well-conserved att segments. This nucleotide substitution makes a BstBI recognition site in Frankia attB and was used to localize the recombination site in a 25-bp region going from the anticodon to the T Psi C loop of the tRNA(pro) sequence. Integration of pSAM2 into the Frankia attB site is the first step toward introduction of pSAM2 derivatives into Frankia spp.
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页码:4279 / 4283
页数:5
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