Maeda T, Takada N, Furushita M, Shiba T
Department of Food Science and Technology, National Fisheries University, Shimonoseki, 759-6595, Yamaguchi, Japan.
FEMS Microbiol Lett. 2000 Nov 1;192(1):73-7. doi: 10.1111/j.1574-6968.2000.tb09361.x.
The 16S-23S rRNA intergenic spacers (IGS) of Vibrio parahaemolyticus were PCR-amplified and cloned with pT7Blue T vector. A total of six clones were isolated dependent on size difference. The clones were different with respect to both the number and the composition of the tRNA genes included, and were designated IGS-0, IGS-E, IGS-IA, IGS-AE, IGS-EKV and IGS-EKAV. IGS-EKAV included the cluster of tRNA(Glu)-tRNA(Lys)-tRNA(Ala)-tRNA(Val); IGS-EKV, tRNA(Glu)-tRNA(Lys)-tRNA(Val); IGS-AE, tRNA(Ala)-tRNA(Glu); IGS-IA, tRNA(Ile)-tRNA(Ala); and IGS-E, tRNA(Glu). IGS-0 had no tRNA gene. Some similarities were found in the nucleotide sequence of the non-coding regions flanked by the tRNA genes. The structure difference found in the spacers is meaningful for elucidating the evolutionary line of each ribosomal RNA operon and the profile is applicable as a molecular marker of the bacterium.
对副溶血性弧菌的16S - 23S rRNA基因间隔区(IGS)进行PCR扩增,并用pT7Blue T载体进行克隆。根据大小差异共分离出6个克隆。这些克隆在所含tRNA基因的数量和组成上均有所不同,分别命名为IGS - 0、IGS - E、IGS - IA、IGS - AE、IGS - EKV和IGS - EKAV。IGS - EKAV包含tRNA(Glu)- tRNA(Lys)- tRNA(Ala)- tRNA(Val)簇;IGS - EKV包含tRNA(Glu)- tRNA(Lys)- tRNA(Val);IGS - AE包含tRNA(Ala)- tRNA(Glu);IGS - IA包含tRNA(Ile)- tRNA(Ala);IGS - E包含tRNA(Glu)。IGS - 0没有tRNA基因。在tRNA基因两侧的非编码区核苷酸序列中发现了一些相似性。间隔区发现的结构差异对于阐明每个核糖体RNA操纵子的进化谱系具有重要意义,该图谱可作为该细菌的分子标记。