Department of Food Microbiology, University College, Cork, Ireland.
Appl Environ Microbiol. 1987 Jan;53(1):74-8. doi: 10.1128/aem.53.1.74-78.1987.
The conjugative transposon Tn919, originally isolated in Streptococcus sanguis FC1, is capable of low-frequency transfer (10 and 10 per recipient) on membrane filters to a wide number of streptococcal recipients including the industrially important lactic streptococci. The introduction of pMG600 (Lac Lax; a lactose plasmid capable of conjugative transfer at high frequencies and which, in certain hosts, confers an unusual clumping phenotype) into a Streptococcus lactis CH919 donor, generating S. lactis CH001, resulted in a significant improvement in the transfer frequency of Tn919 to S. lactis CK50 (1.25 x 10 per recipient). In addition, these matings could be performed on agar surfaces, allowing the recovery of a greater number of recipients than with filter matings. Tn919 also transferred at high frequency to S. lactis subsp. diacetylactis 18-16S but not to Streptococcus cremoris strains. Insertion in 18-16S transconjugants generated from filter matings with an S. lactis CH919 donor was random, occurring at different sites on the chromosome and also in plasmid DNA. Thus, the conditions necessary for the practical exploitation of Tn919 in the targeting and cloning of genes from a member of the lactic streptococci, namely, high-frequency delivery and random insertion in host DNA, were achieved.
Tn919 转座子最初从血液链球菌 FC1 中分离出来,能够在膜滤器上以低频率(每个受体 10 和 10)转移到许多链球菌受体,包括工业上重要的乳链球菌。将 pMG600(Lac Lax;一种能够以高频率进行共轭转移的乳糖质粒,在某些宿主中赋予不寻常的聚集表型)引入乳链球菌 CH919 供体,生成乳链球菌 CH001,导致 Tn919 向乳链球菌 CK50 的转移频率显著提高(每个受体 1.25 x 10)。此外,这些交配可以在琼脂表面上进行,允许回收比滤器交配更多的受体。Tn919 还以高频率转移到乳链球菌亚种二乙酰乳酸 18-16S,但不能转移到乳球菌菌株。用乳链球菌 CH919 供体进行滤器交配产生的 18-16S 转导子中的插入是随机的,发生在染色体的不同位置,也发生在质粒 DNA 中。因此,实现了在乳链球菌成员中靶向和克隆基因时 Tn919 的实际利用所需的条件,即高频率传递和在宿主 DNA 中的随机插入。