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作 者:任禛[1] 尹敏 夏体渊[1] 陈泽斌[1] 尹利方 韩丽[1] 靳松[1] 王定康[1]
机构地区:[1]昆明学院农学院/云南省高等学校都市型现代农业工程研究中心,云南昆明650214 [2]云南大学医学院,云南昆明650091
出 处:《西南农业学报》2017年第9期2113-2118,共6页Southwest China Journal of Agricultural Sciences
基 金:云南省应用基础研究自筹基金项目(2013FZ099);云南省高校优势特色重点学科(生态学)建设项目;昆明学院人才引进基金项目(YJL12002);昆明学院校级科学研究一般项目(XJL14018);云南省高校特色生物资源开发与利用重点实验室开放基金项目(GXKJ201623)
摘 要:【目的】本文研究了玫瑰根系的AMF多样性和组成结构。【方法】从昆明学院种质资源圃随机采集玫瑰‘卡罗拉’3株,采用CTAB法提取根系DNA,运用巢式PCR扩增AM真菌部分18S rRNA基因区域,扩增产物混合后构建克隆文库,最终确定30个阳性克隆子测序,并对文库进行评价和分析。【结果】文库Coverage C值为80%,但Rarefaction曲线不够饱和,应加大文库克隆子数目;文库多样性参数香农指数和辛普森指数分别为1.432和0.25,物种丰富度为4.0;以98%为界,30条序列被划分为15个OTU,均为Glomus的种类;其中OTU1是文库中的主要类型,OTU2~OTU9代表了常见类型,而OTU10~OTU15为稀有类型;有10个OTU在系统进化树上单独聚类,代表着Glomus较为新颖的种类。【结论】在玫瑰根系发现的15个OTU全为Glomus的种类,其中主要类型1种,常见类型8种,稀有类型6种,具体分类地位均不清楚。[ Objective] The AMF diversity and composition structure of roses root were studied in this paper. [ Method] Three ' Rosa Carola'plant were randomly collected from germplasm resources gardon of Kunming college. The roots DNA were extracted using CTAB method andAMF partial 18S rRNA gene were amplified by Nested-PCR. The DNA mixture was used to construct AMF clone library. Finally, thirty posi-five clones were chosen for sequencing and analyzed. Meanwhile, e/one library was evaluated and analyzed in this paper. [ Result1 CoverageC value of the library was 70.0 %, but the rarefaction curve was not saturated, and the number of library clones should be increased. TheShannon index and Simpson index was 1. 432 and 0.25, respectively, and the species richness was 4. O. Sequences with 〉98 % similaritywere assigned to the same OTUs. Totally, 30 sequences were divided into 15 OTUs and all of them belonged to Glomus. Among them, OTU1was the main type of library, OTU2 - OTU9 represented the common types, while OTUIO - OTU15 were rare types. 10 OTUs which clus-tered separately represented the Glomus novel types. [ Conclusion] The AMF found in the roots of 'Rosa Carola' were all G/omus species.Among them, there were 1 main type, 8 common types and 6 rare types. The classification status of all clones was not clear.
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