Pettersson B, Johansson K E, Uhlén M
Department of Biochemistry and Biotechnology, Royal Institute of Technology, Stockholm, Sweden.
Appl Environ Microbiol. 1994 Jul;60(7):2456-61. doi: 10.1128/aem.60.7.2456-2461.1994.
Automated solid-phase DNA sequencing was used for determination of partial 16S ribosomal DNA sequences of mycoplasmas. The sequence information was used to establish phylogenetic relationships of 11 different mycoplasmas whose 16S rRNA sequences had not been determined earlier. A biotinylated fragment corresponding to positions 344 to 939 in the Escherichia coli sequence was generated by PCR. The PCR product was immobilized onto streptavidin-coated paramagnetic beads, and direct sequencing was performed in both directions. One previously unclassified avian mycoplasma was found to belong to the Mycoplasma lipophilum cluster of the hominis group. Microheterogeneities were discovered in the rRNA operons of Mycoplasma mycoides subsp. mycoides (SC type), confirming the existence of two different rRNA operons. The 16S rRNA sequence of M. mycoides subsp. capri was identical to that of M. mycoides subsp. mycoides (type SC), except that no microheterogeneities were revealed. Furthermore, automated solid-phase DNA sequencing was used to identify a mycoplasmal contamination of a cell culture as Mycoplasma hyorhinis, which proved to be very difficult by conventional methods. The results suggest that the direct solid-phase DNA sequencing procedure is a powerful tool for identification of mycoplasmas and is also useful in taxonomic studies.
采用自动化固相DNA测序法测定支原体16S核糖体DNA的部分序列。该序列信息用于建立11种不同支原体的系统发育关系,这些支原体的16S rRNA序列此前尚未确定。通过PCR生成了与大肠杆菌序列中第344至939位相对应的生物素化片段。将PCR产物固定在链霉亲和素包被的顺磁珠上,并进行双向直接测序。发现一种先前未分类的禽支原体属于人型支原体嗜脂支原体簇。在丝状支原体丝状亚种(SC型)的rRNA操纵子中发现了微异质性,证实存在两种不同的rRNA操纵子。山羊支原体的16S rRNA序列与丝状支原体丝状亚种(SC型)的序列相同,只是未发现微异质性。此外,利用自动化固相DNA测序法鉴定出细胞培养物中的支原体污染为猪鼻支原体,而传统方法证明这非常困难。结果表明,直接固相DNA测序程序是鉴定支原体的有力工具,在分类学研究中也很有用。