Wijaya Agus, Hermann Anette, Abriouel Hikmate, Specht Ingrid, Yousif Nuha M K, Holzapfel Wilhelm H, Franz Charles M A P
Federal Research Centre for Nutrition and Food, Institute of Hygiene and Toxicology, Haid-und-Neu-Strasse 9, D-76131 Karlsruhe, Germany.
J Food Prot. 2004 Dec;67(12):2772-8. doi: 10.4315/0362-028x-67.12.2772.
Enterococcus faecium strain FAIR-E 345 isolated from food was shown to possess bile salt hydrolase (Bsh) activity in a plate screening assay and by high-performance liquid chromatography analysis. The bsh gene was cloned and sequenced. DNA sequence analysis revealed that it encoded a protein of 324 amino acids, with pI 4.877. A bsh gene probe was prepared from the cloned bsh gene and was used for probing plasmid and total genomic DNA of Bsh-positive enterococci isolated from food to determine the genomic location of their bsh genes. This probe was able to detect the bsh gene among total genomic DNA preparations but not from plasmid preparations of 10 plasmid-bearing Enterococcus strains. However, the probe could detect the bsh gene from total genomic DNA preparations of 12 Enterococcus strains that did not contain detectable plasmid DNA. In no cases did the probe hybridize with plasmid DNA preparations, suggesting that the bsh gene among enterococci is probably generally chromosomally encoded. This presumptive chromosomal location of bsh genes among food enterococci suggests that transfer of this trait by conjugative plasmids is unlikely.
从食品中分离出的屎肠球菌菌株FAIR-E 345在平板筛选试验和高效液相色谱分析中显示具有胆汁盐水解酶(Bsh)活性。对bsh基因进行了克隆和测序。DNA序列分析表明,它编码一个由324个氨基酸组成的蛋白质,其等电点为4.877。从克隆的bsh基因制备了bsh基因探针,并用于探测从食品中分离出的Bsh阳性肠球菌的质粒和总基因组DNA,以确定其bsh基因的基因组位置。该探针能够在总基因组DNA制剂中检测到bsh基因,但在10株携带质粒的肠球菌的质粒制剂中未检测到。然而,该探针可以从12株不含可检测质粒DNA的肠球菌的总基因组DNA制剂中检测到bsh基因。在任何情况下,该探针都未与质粒DNA制剂杂交,这表明肠球菌中的bsh基因可能通常是由染色体编码的。食品肠球菌中bsh基因的这种推测性染色体定位表明,通过接合质粒转移该性状的可能性不大。