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作 者:陈源源[1] 陈浩[1] 石贵阳[1] 王正祥[1]
机构地区:[1]江南大学生物工程学院工业生物技术教育部重点实验室
出 处:《食品与发酵工业》2012年第4期11-14,共4页Food and Fermentation Industries
基 金:国家自然资源科技平台(No.2005DKA21208);教育部科技基础条件平台(No.505006)资助
摘 要:内部转录间隔区(internal transcribed spacer,ITS)序列是目前最常用的酵母分子鉴定标识之一。该文利用ITS序列同源性分析法对保藏于中国高校工业微生物资源与信息中心的623株酵母分离物进行了鉴定。实验结果显示:581株酵母分离物(93.3%)可通过ITS序列直接鉴定到种一级,40株分离物(6.4%)可鉴定至属一级,仅有2株酵母分离物无法通过ITS序列获得有效鉴定。上述结果表明,ITS序列在大多数酵母种属鉴定中具有很高的敏感性和特异性,可以作为第一分子标识用于大批量酵母分离物的分子鉴定。The internal transcribed spacer (ITS) region of nuclear DNA is one of the most used locus for yeast i- dentification with growing sequence data deposited in public-access databases. This study extensively evaluated the feasibility of ITS sequence analysis for systemic classification of yeast isolates. The ITS regions of 623 yeast strains de- posited in CICIM-CU were amplified by PCR and sequenced, the sequences were compared to reference data available at the GenBank database by using BLAST. Most of fungal isolates (93.3%) were assigned to species level successful- ly. 40 strains (6.4%) were only can be assigned to genus level. 2 strains cannot be identified based on ITS se- quences analysis. This study shown ITS sequences were sufficiently sensitive for identifying most of yeasts, it can be powerfully and ordinarily used as first-round barcoding gene to systemic identification of bulk yeast isolates.
分 类 号:TQ926[轻工技术与工程—发酵工程]
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