Characterization of a periplasmic ATP-binding cassette iron import system of Brachyspira (Serpulina) hydodysenteriae

被引:19
作者
Dugourd, D
Martin, C
Rioux, CR
Jacques, M
Harel, J [1 ]
机构
[1] Univ Montreal, Fac Med Vet, Dept Pathol & Microbiol, Grp Rech Malad Infect Porc, St Hyacinthe, PQ J2S 7C6, Canada
[2] INRA, Microbiol Lab, F-63122 St Genes Champanelle, France
[3] CHU Quebec, Ctr Rech Infectiol, Quebec City, PQ G1V 4G2, Canada
关键词
D O I
10.1128/JB.181.22.6948-6957.1999
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The nucleotide sequence of the pathogenic spirochete Brachyspira hyodysenteriae bit (for "Brachyspira iron transport") genomic region has been determined. The bit region is likely to encode an iron ATP-binding cassette transport system with some homology to those encountered in gram-negative bacteria. Six open reading frames oriented in the same direction and physically linked have been identified. This system possesses a protein containing ATP-binding motifs (BitD), two hydrophobic cytoplasmic membrane permeases (BitE and BitF), and at least three lipoproteins (BitA, BitB, and BitC) with homology to iron periplasmic binding proteins. These periplasmic binding proteins exhibit lipoprotein features. They are labeled by [H-3]palmitate when tested in recombinant Escherichia coli, and their signal peptides are typical for substrates of the type II secretory peptidase. The FURTA system and Congo red assay indicate that BitB and BitC are involved in iron binding. The Bit system is detected only in B. hyodysenteriae and is absent from B. innocens and B. pilosicoli.
引用
收藏
页码:6948 / 6957
页数:10
相关论文
共 73 条
[41]   IDENTIFICATION OF AN IRON-REGULATED 37,000-DALTON PROTEIN IN THE CELL-ENVELOPE OF NEISSERIA-GONORRHOEAE [J].
MIETZNER, TA ;
LUGINBUHL, GH ;
SANDSTROM, E ;
MORSE, SA .
INFECTION AND IMMUNITY, 1984, 45 (02) :410-416
[42]   CLONING AND EXPRESSION OF A SERPULA (TREPONEMA) HYODYSENTERIAE HEMOLYSIN GENE [J].
MUIR, S ;
KOOPMAN, MBH ;
LIBBY, SJ ;
JOENS, LA ;
HEFFRON, F ;
KUSTERS, JG .
INFECTION AND IMMUNITY, 1992, 60 (02) :529-535
[43]   MICROBIAL IRON COMPOUNDS [J].
NEILANDS, JB .
ANNUAL REVIEW OF BIOCHEMISTRY, 1981, 50 :715-731
[44]  
NEILANDS JB, 1994, METHOD ENZYMOL, V235, P344
[45]   Transposon mutagenesis: Cloning of chromosomal DNA from the site of Tn916 insertion using polymerase chain reaction [J].
Novak, J ;
Novak, L ;
Shah, GR ;
Woodruff, WA ;
Caufield, PW .
BIOTECHNOLOGY TECHNIQUES, 1997, 11 (01) :51-54
[46]   MOLECULAR-CLONING AND EXPRESSION OF RICKETTSIA-TSUTSUGAMUSHI GENES FOR 2 MAJOR PROTEIN ANTIGENS IN ESCHERICHIA-COLI [J].
OAKS, EV ;
STOVER, CK ;
RICE, RM .
INFECTION AND IMMUNITY, 1987, 55 (05) :1156-1162
[47]   Unification of the genera Serpulina and Brachyspira, and proposals of Brachyspira hyodysenteriae comb nov, Brachyspira innocens comb nov and Brachyspira pilosicoli comb nov [J].
Ochiai, S ;
Adachi, Y ;
Mori, K .
MICROBIOLOGY AND IMMUNOLOGY, 1997, 41 (06) :445-452
[48]   GENETIC ORGANIZATION OF MULTIPLE FEP GENES ENCODING FERRIC ENTEROBACTIN TRANSPORT FUNCTIONS IN ESCHERICHIA-COLI [J].
OZENBERGER, BA ;
NAHLIK, MS ;
MCINTOSH, MA .
JOURNAL OF BACTERIOLOGY, 1987, 169 (08) :3638-3646
[49]   DETECTION AND DIFFERENTIATION OF IRON-RESPONSIVE AVIRULENT MUTANTS ON CONGO RED AGAR [J].
PAYNE, SM ;
FINKELSTEIN, RA .
INFECTION AND IMMUNITY, 1977, 18 (01) :94-98