Characterization of the locus encoding the Streptococcus pneumoniae type 19F capsular polysaccharide biosynthetic pathway

被引:98
作者
Morona, JK
Morona, R
Paton, JC
机构
[1] WOMENS & CHILDRENS HOSP,MOL MICROBIOL UNIT,ADELAIDE,SA 5006,AUSTRALIA
[2] UNIV ADELAIDE,DEPT MICROBIOL & IMMUNOL,ADELAIDE,SA 5005,AUSTRALIA
关键词
D O I
10.1046/j.1365-2958.1997.2551624.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have previously reported the nucleotide sequence of the first six genes of the Streptococcus pneumoniae type 19F capsular polysaccharide biosynthesis locus (cps19f). In this study we used plasmid insertion/rescue and inverse polymerase chain reaction (PCR) to clone an additional 10 kb downstream region containing the remainder of the cps19f locus, which was then subjected to sequence analysis. The cps19f locus is located in the S. pneumoniae chromosome between dexB and aliA, and consists of 15 open reading frames (ORFs), designated cps19fA to cps19fO, that appear to be arranged as a single transcriptional unit. Insertion-duplication mutants in seven out of the nine new ORFs have been constructed in a smooth type 19F strain, all of which resulted in a rough (nonencapsulated) phenotype, confirming that the operon is essential for capsule production. Comparison with sequence databases has allowed us to propose functions for 12 of the cps19f gene products, and a biosynthetic pathway for type 19F capsular polysaccharide. T7 expression studies confirmed that cps19fH, cps19fK, cps19fL, cps19fM and cps19fN directed the production of polypeptides of the expected size In Escherichia coli. The function of the cps19fK product was confirmed by its ability to complement a mutation in nfrC (rffE) in E. coli, as judged by restoration of sensitivity to bacteriophage N4. Interestingly, the last four genes of the locus (cps19fL-O) exhibit very strong homology (up to 70% amino acid identity) to a portion of the Shigella flexneri rfb gene cluster encoding biosynthesis of dTDP-rhamnose. When expressed in E. coli, cps19fL-O were capable of complementing a mutation, deleting the respective Shigella flexneri homologues. Southern hybridization analysis indicated that cps19fA and cps19fB were the only cps genes found in all 16 S. pneumoniae serotypes/groups tested. The region from cps19fG to cps19fK was found only in members of serogroup 19, and, within this, cps19fl was unique to type 19F.
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页码:751 / 763
页数:13
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共 58 条
[1]   3 HIGHLY HOMOLOGOUS MEMBRANE-BOUND LIPOPROTEINS PARTICIPATE IN OLIGOPEPTIDE TRANSPORT BY THE AMI SYSTEM OF THE GRAM-POSITIVE STREPTOCOCCUS-PNEUMONIAE [J].
ALLOING, G ;
DEPHILIP, P ;
CLAVERYS, JP .
JOURNAL OF MOLECULAR BIOLOGY, 1994, 241 (01) :44-58
[2]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[3]   Sequence and transcriptional analysis of a DNA region involved in the production of capsular polysaccharide in Streptococcus pneumoniae type 3 [J].
Arrecubieta, C ;
Garcia, E ;
Lopez, R .
GENE, 1995, 167 (1-2) :1-7
[4]  
AUSTRIAN R, 1981, REV INFECT DIS, V3, pS1
[5]   SIMULTANEOUS PRODUCTION OF .2. CAPSULAR POLYSACCHARIDES BY PNEUMOCOCCUS .2. THE GENETIC AND BIOCHEMICAL BASES OF BINARY CAPSULATION [J].
AUSTRIAN, R ;
BERNHEIMER, HP ;
SMITH, EEB ;
MILLS, GT .
JOURNAL OF EXPERIMENTAL MEDICINE, 1959, 110 (04) :585-602
[6]  
AVERY OSWALD T., 1931, JOUR EXP MED, V54, P73, DOI 10.1084/jem.54.1.73
[7]   REDUCED VIRULENCE OF A DEFINED PNEUMOLYSIN-NEGATIVE MUTANT OF STREPTOCOCCUS-PNEUMONIAE [J].
BERRY, AM ;
YOTHER, J ;
BRILES, DE ;
HANSMAN, D ;
PATON, JC .
INFECTION AND IMMUNITY, 1989, 57 (07) :2037-2042
[8]  
BROWN MGM, 1979, FEMS MICROBIOL LETT, V5, P219
[9]   MOLECULAR ANALYSIS OF THE RFB-GENE CLUSTER OF SALMONELLA SEROVAR MUENCHEN (STRAIN M67) - THE GENETIC-BASIS OF THE POLYMORPHISM BETWEEN GROUP-C-2 AND GROUP-B [J].
BROWN, PK ;
ROMANA, LK ;
REEVES, PR .
MOLECULAR MICROBIOLOGY, 1992, 6 (10) :1385-1394
[10]   MOLECULAR-CLONING, CHARACTERIZATION, AND NUCLEOTIDE-SEQUENCE OF THE RFC GENE, WHICH ENCODES AN O-ANTIGEN POLYMERASE OF SALMONELLA-TYPHIMURIUM [J].
COLLINS, LV ;
HACKETT, J .
JOURNAL OF BACTERIOLOGY, 1991, 173 (08) :2521-2529