Characterisation of IS153, an IS3-family insertion sequence isolated from Lactobacillus sanfranciscensis and its use for strain differentiation

被引:17
作者
Ehrmann, MA [1 ]
Vogel, RF [1 ]
机构
[1] Tech Univ Munich, Lehrstuhl Tech Mikrobiol, D-85350 Freising Weihenstephan, Germany
关键词
insertion element; Lactobacillus sanfranciscensis; strain differentiation; EMBL AJ239042;
D O I
10.1078/0723-2020-00057
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
An insertion sequence has been identified in the genome of Lactobacillus sanfranciscensis DSM 20451(T) as segment of 1351 nucleotides containing 37-bp imperfect terminal inverted repeats. The sequence of this element encodes two out of phase, overlapping open reading frames, orfA and orfB, from which three putative proteins are produced. OrfAB is a transframe protein produced by -1 translational frame shifting between orf A and orf B that is presumed to be the transposase. The large orfAB of this element encodes a 342 amino acid protein that displays similarities with transposases encoded by bacterial insertion sequences belonging to the IS3 family. In L. sanfranciscensis type strain DSM 20451(T) multiple truncated IS elements were identified. Inverse PCR was used to analyze target sites of four of these elements, but except of their highly AT rich character not any sequence specificity was identified so far. Moreover, no flanking direct repeats were identified. Multiple copies of IS153 were detected by hybridization in other strains of L. sanfranciscensis. Resulting hybridization patterns were shown to differentiate between organisms at strain level rather than a probe targeted against the 16S rDNA. With a PCR based approach IS153 or highly similar sequences were detected in L. acidophilus, L. casei, L. malefermentans, L. plantarum, L. hilgardii, L. collinoides L. farciminis L. sakei and L. salivarius, L. reuteri as well as in. Enterococcus faecium, Pediococcus acidilactici and P. pentosaceus.
引用
收藏
页码:443 / 450
页数:8
相关论文
共 37 条
[1]  
Bauer J, 1999, J CLIN MICROBIOL, V37, P442
[2]  
Berg C. M., 1989, Mobile DNA, P879
[3]   PHAGE ABORTIVE INFECTION MECHANISM FROM LACTOCOCCUS-LACTIS SUBSP LACTIS, EXPRESSION OF WHICH IS MEDIATED BY AN ISO-ISS1 ELEMENT [J].
CLUZEL, PJ ;
CHOPIN, A ;
EHRLICH, SD ;
CHOPIN, MC .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1991, 57 (12) :3547-3551
[4]  
Ehrmann MA, 1998, FEMS MICROBIOL LETT, V169, P81, DOI 10.1016/S0378-1097(98)00467-4
[5]   REDUCTION OF BACKGROUND PROBLEMS IN NONRADIOACTIVE NORTHERN AND SOUTHERN BLOT ANALYSES ENABLES HIGHER SENSITIVITY THAN P-32 BASED HYBRIDIZATIONS [J].
ENGLERBLUM, G ;
MEIER, M ;
FRANK, J ;
MULLER, GA .
ANALYTICAL BIOCHEMISTRY, 1993, 210 (02) :235-244
[6]  
Floriano B, 1998, APPL ENVIRON MICROB, V64, P4883
[7]  
GALAS DJ, 1989, MOBILE DNA, P109
[8]  
Gasson M. J., 1994, Genetics and biotechnology of lactic acid bacteria., P1
[9]   CHARACTERIZATION AND DISTRIBUTION OF 2 INSERTION SEQUENCES, IS1191 AND ISO-IS981, IN STREPTOCOCCUS-THERMOPHILUS - DOES INTERGENERIC TRANSFER OF INSERTION SEQUENCES OCCUR IN LACTIC-ACID BACTERIA COCULTURES [J].
GUEDON, G ;
BOURGOIN, F ;
PEBAY, M ;
ROUSSEL, Y ;
COLMIN, C ;
SIMONET, JM ;
DECARIS, B .
MOLECULAR MICROBIOLOGY, 1995, 16 (01) :69-78
[10]   INSERTION ELEMENTS ON LACTOCOCCAL PROTEINASE PLASMIDS [J].
HAANDRIKMAN, AJ ;
VANLEEUWEN, C ;
KOK, J ;
VOS, P ;
DEVOS, WM ;
VENEMA, G .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1990, 56 (06) :1890-1896