{"title":"工业曲霉真菌的分离鉴定及aflR基因分析","authors":"D. Wei","doi":"10.7099/FS.200312.0133","DOIUrl":null,"url":null,"abstract":"One hundred and forty-six strains of Aspergillus sp. were isolated and identified from 27 commercial koji which were used in producing fermented foods in Taiwan. None was found to produce aflatoxin. The genomic DNA of 17 randomly selected Aspergilli were extracted and amplified by PCR using a pair of primers, which annealed part of the coding region of aflR gene, to investigate whether the non-production of aflatoxin is caused by the absence of an aflR gene. The results indicate that all the examined nonaflatoxigenic isolates contained the regulatory gene aflR. Gene analysis revealed that the two distinct patterns of fingerprints, T-GA- A-*-C and C-C-C-C-C-T at position –90, –89, –72, –61, –43, and 102, described by Chang et al. (1995), could not differentiate all the examined strains that were classified in the Aspergillus Section Flavi.","PeriodicalId":12667,"journal":{"name":"Fungal Science","volume":"51 1","pages":"133-143"},"PeriodicalIF":0.0000,"publicationDate":"2003-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Isolation, identification and aflR gene analysis of industrial Aspergillus fungi\",\"authors\":\"D. Wei\",\"doi\":\"10.7099/FS.200312.0133\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"One hundred and forty-six strains of Aspergillus sp. were isolated and identified from 27 commercial koji which were used in producing fermented foods in Taiwan. None was found to produce aflatoxin. The genomic DNA of 17 randomly selected Aspergilli were extracted and amplified by PCR using a pair of primers, which annealed part of the coding region of aflR gene, to investigate whether the non-production of aflatoxin is caused by the absence of an aflR gene. The results indicate that all the examined nonaflatoxigenic isolates contained the regulatory gene aflR. Gene analysis revealed that the two distinct patterns of fingerprints, T-GA- A-*-C and C-C-C-C-C-T at position –90, –89, –72, –61, –43, and 102, described by Chang et al. (1995), could not differentiate all the examined strains that were classified in the Aspergillus Section Flavi.\",\"PeriodicalId\":12667,\"journal\":{\"name\":\"Fungal Science\",\"volume\":\"51 1\",\"pages\":\"133-143\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2003-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fungal Science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.7099/FS.200312.0133\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fungal Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7099/FS.200312.0133","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
从台湾27种用于发酵食品生产的商品曲中分离鉴定出146株曲霉。没有发现会产生黄曲霉毒素。随机选取17株曲霉提取基因组DNA,利用一对引物对aflR基因的部分编码区进行退火,通过PCR扩增,探讨不产生黄曲霉毒素是否是由于缺少aflR基因引起的。结果表明,所有非黄曲霉毒素分离株均含有调控基因aflR。基因分析表明Chang et al.(1995)描述的- 90、- 89、- 72、- 61、- 43和102位点的T-GA- A-*- c和c - c - c - t两种不同的指纹图谱不能区分所有被分类在黄曲霉节中的菌株。
Isolation, identification and aflR gene analysis of industrial Aspergillus fungi
One hundred and forty-six strains of Aspergillus sp. were isolated and identified from 27 commercial koji which were used in producing fermented foods in Taiwan. None was found to produce aflatoxin. The genomic DNA of 17 randomly selected Aspergilli were extracted and amplified by PCR using a pair of primers, which annealed part of the coding region of aflR gene, to investigate whether the non-production of aflatoxin is caused by the absence of an aflR gene. The results indicate that all the examined nonaflatoxigenic isolates contained the regulatory gene aflR. Gene analysis revealed that the two distinct patterns of fingerprints, T-GA- A-*-C and C-C-C-C-C-T at position –90, –89, –72, –61, –43, and 102, described by Chang et al. (1995), could not differentiate all the examined strains that were classified in the Aspergillus Section Flavi.