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高通量测序分析混合菌群中的呕吐毒素降解菌
引用本文:高慧,牛家峰,杨华,陆兆新,陈美容,吕凤霞. 高通量测序分析混合菌群中的呕吐毒素降解菌[J]. 食品科学, 2021, 42(24): 123-130. DOI: 10.7506/spkx1002-6630-20210316-212
作者姓名:高慧  牛家峰  杨华  陆兆新  陈美容  吕凤霞
作者单位:(南京农业大学食品科技学院,江苏 南京 210095)
基金项目:江苏省科技计划项目(BE2018319)
摘    要:为筛选具有降解脱氧雪腐镰刀菌烯醇(deoxynivalenol,DON)能力的微生物,利用高通量测序方法分析混合菌群中的DON降解菌。从土壤中获得具有DON降解能力的混合菌群LG-6,并发现不同梯度稀释倍数的混合菌群之间DON降解效果具有明显差异。稀释至10-7时混合菌群LG-6-7能完全降解DON,而稀释至10-8时混合菌群LG-6-8不能降解DON。对这2?个混合菌群的微生物多样性进行分析,发现混合菌群LG-6-7包括假苍白杆菌属、节细菌属、假单胞菌属、代尔夫特菌属和德沃斯氏菌属,而混合菌群LG-6-8包括假苍白杆菌属和节细菌属。故推测假单胞菌属、德沃斯氏菌属和代尔夫特菌属在降解DON的过程中必不可少。此外,假单胞菌B6-24和德沃斯氏菌A6-243混合培养时,48?h内完全降解DON。该混合菌群培养温度为37?℃、pH?7.0,培养基为MMT培养基,并发现该混合菌群是通过微生物代谢产生的酶对DON进行降解。本研究发现能完全降解DON的假单胞菌B6-24和德沃斯氏菌A6-243混合菌群,为呕吐毒素生物脱毒剂的研发提供一定理论依据。

关 键 词:呕吐毒素;降解;微生物多样性分析;假单胞菌属;德沃斯氏菌属  

High-throughput Sequencing Analysis of Vomitoxin-degrading Bacteria in Bacterial Consortium
GAO Hui,NIU Jiafeng,YANG Hua,LU Zhaoxin,CHEN Meirong,LÜ Fengxia. High-throughput Sequencing Analysis of Vomitoxin-degrading Bacteria in Bacterial Consortium[J]. Food Science, 2021, 42(24): 123-130. DOI: 10.7506/spkx1002-6630-20210316-212
Authors:GAO Hui  NIU Jiafeng  YANG Hua  LU Zhaoxin  CHEN Meirong  LÜ Fengxia
Affiliation:(College of Food Science and Technology, Nanjing Agricultural University, Nanjing 210095, China)
Abstract:Vomitoxin, also known as DON, is a secondary metabolite produced by several Fusarium sp. In order to select microorganisms capable of degrading DON, high-throughput sequencing was used to analyze DON-degrading bacteria in bacterial consortia. In this study, bacterial consortium LG-6 with DON-degrading capacity was obtained from soil, and it was found that the effect varied depending on the dilution ratio of the bacterial consortium. LG-6 diluted by a factor of 10-7 (denoted as LG-6-7) but not 10-8 (denoted as LG-6-8) could completely degrade DON. The analysis of microbial diversity demonstrated that LG-6-7 included Pseudochrobactrum, Pseudomonas, Delftia, Devosia, and Achromobacter, while LG-6-8 included only Pseudochrobactrum and Achromobacte, indicating that Pseudomonas, Devosia and Delftia are essential for the degradation of DON. In addition, DON was completely degraded within 48 h by a bacterial consortium of Pseudomonas sp. B6-24 and Devosia A6-243. The optimal culture conditions for the bacterial consortium were 37 ℃, pH 7.0, and MMT medium. Moreover, microbial enzymes from the consortium were responsible for the degradation of DON. In conclusion, a bacterial consortium of Pseudomonas sp. B6-24 and Devosia A6-243 can degrade DON completely, which will lay a foundation for the research and development of biological detoxifying agents for vomiting toxin.
Keywords:deoxynivalenol   detoxification   microbial diversity analysis   Pseudomonas   Devosia,
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