期刊文献+

复合菌系降解黄曲霉毒素B_1的效果及组成多样性研究 被引量:4

Degradation of Aflatoxin B_1 by a Microbial Consortium and Its Composition and Diversity
下载PDF
导出
摘要 采用"外淘汰法"筛选了一组对黄曲霉毒素B_1(aflatoxin B_1,AFB_1)具有高效降解能力的复合菌系FBAD-2,该复合菌系在120 h内能将质量浓度为2 000μg/L的AFB_1完全降解,对质量浓度为5 000μg/L的AFB_1能降解90%。FBAD-2在30~70℃的范围内均能保持对AFB_1的高效降解能力,其最适温度为60℃。毒素降解实验分析表明,FBAD-2对AFB_1的降解主要是胞外酶的作用,其最适产酶时间为24 h,此时的胞外粗酶液在48 h内能将5 000μg/L的AFB_1完全降解。16S rDNA基因组测序分析结果表明,FBAD-2的微生物组成主要包括土芽孢杆菌(Geobacillus)、嗜热小杆菌(Symbiobacterium thermopilum)、梭菌(Clostridium)和热厌氧杆菌(Tepidanaerobacter)等。 External elimination method was applied to obtain an efficient aflatoxin B1-degrading microbial consortium,designated FBAD-2.The degradation rates of2000and5000μg/L AFB1by the microbial consortium could reach100%and90%within120h,respectively.The toxin degradation ability of FBAD-2was kept at a high level in the range of30-70℃,with an optimal temperature of60℃.The results of AFB1detoxification experiment showed that the extracellular enzymes in the supernatant played a major role in the degradation of AFB1.Furthermore,the optimal culture time for enzyme production was24h,and the supernatant could completely degrade5000μg/L AFB1within48h.16S rRNA gene clone library analysis showed that FBAD-2was mainly composed of bacteria from the genera Geobacillus,Symbiobacterium thermopilum,Clostridium and Tepidanaerobacter.
作者 赵春霞 王轶 程薇 吕育财 龚大春 郭鹏 ZHAO Chunxia;WANG Yi;CHENG Wei;Lü Yucai;GONG Dachun;GUO Peng(College of Biology and Pharmacy, China Three Gorges University, Yichang 443002, China;Institute of Processing of Agricultural Produce and Nuclear Agricultural Research, Hubei Academy of Agricultural Sciences, Wuhan 430064, China)
出处 《食品科学》 EI CAS CSCD 北大核心 2017年第9期106-112,共7页 Food Science
基金 公益性行业(农业)科研专项(201303080) 武汉市科技人才培育计划晨光计划项目(2015070404010189) 武汉市第四批"黄鹤英才计划"项目(武人才[2016]1号) 湖北省科技支撑计划项目(2015BBA199) 湖北省农业科技创新中心创新团队项目(2015-620-007-001)
关键词 黄曲霉毒素B1 生物降解 复合菌系 微生物组成多样性 aflatoxins B1 degradation bacterial community microbial composition and diversity
  • 相关文献

参考文献11

二级参考文献150

共引文献396

同被引文献93

引证文献4

二级引证文献33

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部