Monciardini Paolo, Sosio Margherita, Cavaletti Linda, Chiocchini Claudia, Donadio Stefano
Biosearch Italia, via R. Lepetit 34, 21040 Gerenzano (VA), Italy.
FEMS Microbiol Ecol. 2002 Dec 1;42(3):419-29. doi: 10.1111/j.1574-6941.2002.tb01031.x.
Actinomycetes play a relevant role in soil ecology and are also of important biotechnological interest as they produce several bioactive metabolites. Within the filamentous actinomycetes, it would be desirable to recognize and characterize environmental samples containing unusual genera. To this end, we have developed selective primer sets for polymerase chain reaction (PCR) amplification of 16S rDNA from the Actinomycetales families Micromonosporaceae, Streptomycetaceae, Streptosporangiaceae and Thermomonosporaceae, and from the genus Dactylosporangium. Each primer set, evaluated on genomic DNA from reference strains, showed high specificity and good sensitivity. After amplification of DNA extracted from soil samples, the sequence of the cloned PCR products confirmed the specific amplification of the desired group of sequences in at least 95% of the clones for each primer set. The application of these primers to environmental samples showed the frequent occurrence of these groups in soil samples and also revealed sequences that can be attributed to new groups of actinomycetes.
放线菌在土壤生态学中发挥着重要作用,并且由于它们能产生多种生物活性代谢产物,在生物技术领域也具有重要意义。在丝状放线菌中,识别和鉴定含有不寻常属的环境样本是很有必要的。为此,我们开发了用于聚合酶链反应(PCR)扩增的选择性引物组,用于扩增来自小单孢菌科、链霉菌科、链孢囊菌科和嗜热单孢菌科以及指孢囊菌属的放线菌目家族的16S rDNA。每个引物组在参考菌株的基因组DNA上进行评估,均显示出高特异性和良好的灵敏度。从土壤样本中提取的DNA经扩增后,克隆的PCR产物序列证实,每个引物组至少95%的克隆中都能特异性扩增出所需的序列组。将这些引物应用于环境样本,结果表明这些菌群在土壤样本中频繁出现,同时还揭示了可归因于新放线菌群的序列。