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机构地区:[1]华南理工大学生物科学与工程学院,广州510640
出 处:《微生物学通报》2007年第3期508-511,共4页Microbiology China
基 金:广东省自然科学基金项目(No.04020061);广东省科技攻关项目(No.2004B20201011)
摘 要:以米曲霉沪酿3.042(AS3.951)、酱油曲霉AS3.495为参照,对从商品酱油曲精中分离到的8株酱油生产菌进行RAPD分析。实验筛选到6个扩增产物谱带多、特征好、覆盖面广的引物:Primer1、Primer5、Primer6、Primer7、Primer8、Primer9,重复实验证明其RAPD-PCR扩增图谱具有较好的稳定性,扩增产物谱带一般4~8条,各实验菌株主带1~4条,次带丰富。根据RAPD-PCR扩增图谱构建的系统进化树较好地吻合了传统的形态分类学,证实了RAPD分子标记在酱油生产菌系统发育分析中应用的可行性。RAPD analysis of eight soy sauce strains isolated from commercial soy sauce koji was done with random primers,using Aspergillus oryzae AS3.951 and Aspergillus sojae AS3.495 as controls. Six appropriate primers ( Primerl, Primer5, Primer6, Primer7, Primer8, Primer9) for RAPD-PCR were screened from nine random primers, and repetitive experiments demonstrated that their RAPD-PCR polymorphic patterns were stable. There were usually 4 - 8 bands in their RADP-PCR patterns, where the number of the main bands was 1 - 4 and the secondary bands were abundant. The phylogenetic tree of these strains was reconstructed according to their RAPD-PCR patterns, and it basically corresponded to traditional morphological taxology, demonstrating that the application of RAPD molecular marker in the phylogenetic analysis of soy sauce strains was feasible.
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