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葡萄酒有孢汉逊酵母属分子指纹图谱分析
引用本文:田进,吴成,杨金仙,王春晓. 葡萄酒有孢汉逊酵母属分子指纹图谱分析[J]. 菌物学报, 2020, 39(4): 755-765. DOI: 10.13346/j.mycosystema.190404
作者姓名:田进  吴成  杨金仙  王春晓
作者单位:贵州大学酿酒与食品工程学院 贵州省发酵工程与生物制药重点实验室 贵州 贵阳 550025
基金项目:国家自然科学基金;贵州省科技计划;贵州大学引进人才科研项目;贵州大学大学生SRT计划项目;贵州省教育厅青年科技人才成长项目
摘    要:为分析中国本土野生有孢汉逊酵母属Hanseniaspora酵母菌的种间差异和种内差异,构建分子指纹图谱,为优良有孢汉逊酵母资源的遗传多样性分析及开发利用提供科学依据。采用依赖于培养的经典方法包含WL营养培养基、26S rRNA基因D1/D2区域序列分析和5.8S-ITS-RFLP分析进行118株贵州紫云县刺葡萄自然发酵过程中分离的有孢汉逊酵母属酵母菌种水平的鉴定。采用Tandem repeat-tRNA(TRtRNA)指纹图谱法研究有孢汉逊酵母属酵母在两对微卫星引物扩增下的分子指纹图谱,并利用DPS软件分析不同分子指纹图谱类别之间的遗传发育关系。结果表明,118株贵州紫云县刺葡萄自然发酵过程中分离的野生有孢汉逊酵母属酵母菌,经依赖于培养的经典方法鉴定为3个种,包括Hanseniaspora opuntiaeH. uvarumH. occidentalis。TRtRNA指纹图谱法的引物对一TtRNASC和5CAG扩增出5类图谱,而引物对二TtRNASC和ISSR-MB扩增出10类图谱,可以表现出所测118株有孢汉逊酵母属的种间差异和种内差异。其中种内差异主要表现在H. uvarum中。总体而言,贵州紫云县刺葡萄自然发酵过程中分离的有孢汉逊酵母属主要为H. opuntiaeH. uvarumH. occidentalis,其中H. opuntiaeH. uvarum内部表现了不同的TRtRNA分子指纹图谱,表征了种内遗传多样性。

关 键 词:Hanseniasporaopuntiae  H.uvarum  Tandemrepeat-tRNA指纹图谱法  非酿酒酵母  混合接种发酵  
收稿时间:2019-11-07

The molecular fingerprinting analysis of Hanseniaspora in wine
Jin TIAN,Cheng WU,Jin-Xian YANG,Chun-Xiao WANG. The molecular fingerprinting analysis of Hanseniaspora in wine[J]. Mycosystema, 2020, 39(4): 755-765. DOI: 10.13346/j.mycosystema.190404
Authors:Jin TIAN  Cheng WU  Jin-Xian YANG  Chun-Xiao WANG
Affiliation:Province Key Laboratory of Fermentation Engineering and Biopharmacy, School of Liquor and Food Engineering, Guizhou University, Guiyang, Guizhou 550025, China
Abstract:Interspecies and intraspecies differences of indigenous Hanseniaspora in China are analyzed, and molecular fingerprinting profiles of the Hanseniaspora strains are built. Classical culture-dependent methods including WL nutrient agar, D1/D2 sequencing of 26S rRNA gene and 5.8S-ITS-RFLP analysis were used to identify 118 Hanseniaspora strains isolated from spontaneous fermentation of Vitis davidii in Ziyun of Guizhou province at species level. Tandem repeat-tRNA (TRtRNA) fingerprinting method was used to study molecular fingerprinting profiles of Hanseniaspora strains amplified with two pairs of microsatellite primers. The DPS software was further applied to analyze the phylogenetic correlation among different molecular fingerprinting profiles. The results showed that 118 Hanseniaspora strains identified by classical culture-dependent methods included H. opuntiae, H. uvarum and H. occidentalis. Five profiles were obtained by amplification with primer pair one TtRNASC and 5CAG, and ten profiles were obtained with primer pair two TtRNASC and ISSR-MB. Therefore, TRtRNA fingerprinting method could exhibit the interspecies and intraspecies differences of 118 Hanseniaspora strains. The intraspecies differences were largely indicated in H. uvarum strains. Both H. opuntiae and H. uvarum strains showed different TRtRNA fingerprinting profiles within species, manifesting their intraspecific genetic diversity.
Keywords:Hanseniaspora opuntiae   H. uvarum  tandem repeat-tRNA fingerprinting method  non-Saccharomyces yeast  mixed fermentation  
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