Comparative analysis of the exopolysaccharide biosynthesis gene clusters from four strains of Lactobacillus rhamnosus

被引:94
作者
Péant, B
LaPointe, G
Gilbert, C
Atlan, D
Ward, P
Roy, D
机构
[1] Univ Laval, STELA Dairy Res Ctr, Quebec City, PQ G1K 7P4, Canada
[2] Univ Laval, INAF, Quebec City, PQ G1K 7P4, Canada
[3] Univ Lyon 1, INSA, CNRS, UMR 5122,Lab Microbiol & Genet Mol, F-69622 Villeurbanne, France
[4] Agr & Agri Food Canada, Ctr Food Res & Dev, St Hyacinthe, PQ J2S 8E3, Canada
[5] Notre Dame Hosp, Montreal, PQ H2L 4M1, Canada
来源
MICROBIOLOGY-SGM | 2005年 / 151卷
关键词
D O I
10.1099/mic.0.27852-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The exopolysaccharide (EPS) biosynthesis gene clusters of four Lactobacillus rhamnosus strains consist of chromosomal DNA regions of 18.5 kb encoding 17 ORFs that are highly similar among the strains. However, under identical conditions, EPS production varies considerably among these strains, from 61 to 1611 mg l(-1). Fifteen genes are co-transcribed starting from the first promoter upstream of wzd. Nevertheless, five transcription start sites were identified by 5'-RACE PCR analysis, and these were associated with promoter sequences upstream of wzd, rmlA, welE, wzr and wzb. Six potential glycosyltransferase genes were identified that account for the assembly of the heptasaccharide repeat unit containing an unusually high proportion of rhamnose. Four genes involved in the biosynthesis of the sugar nucleotide precursor dTDP-L-rhamnose were identified in the EPS biosynthesis locus, which is unusual for lactic acid bacteria. These four genes are expressed from their own promoter (P2), as well as co-transcribed with the upstream EPS genes, resulting in coordinated production of the rhamnose precursor with the enzymes involved in EPS biosynthesis. This is believed to be the first report demonstrating that the sequence, original organization and transcription of genes encoding EPS production are highly similar among four strains of Lb. rhamnosus, and do not vary with the amount of EPS produced.
引用
收藏
页码:1839 / 1851
页数:13
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