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用于研究黄曲霉和寄生曲霉中黄曲霉毒素生物合成机制的基因谱分析。

Gene profiling for studying the mechanism of aflatoxin biosynthesis in Aspergillus flavus and A. parasiticus.

作者信息

Yu Jiujiang, Ronning Catherine M, Wilkinson Jeffery R, Campbell Bruce C, Payne Gary A, Bhatnagar Deepak, Cleveland Thomas E, Nierman William C

机构信息

USDA/ARS, Southern Regional Research Center, New Orleans, LA 70124, USA.

出版信息

Food Addit Contam. 2007 Oct;24(10):1035-42. doi: 10.1080/02652030701513800.

Abstract

Aflatoxins are toxic and carcinogenic polyketide metabolites produced by certain fungal species, including Aspergillus flavus and A. parasiticus. Many internal and external factors, such as nutrition and environment affect aflatoxin biosynthesis; therefore, we analyzed the transcriptome of A. flavus using expressed sequence tags (ESTs) from a normalized cDNA expression library constructed from mycelia harvested under several conditions. A total of 7218 unique ESTs were identified from 26,110 sequenced cDNA clones. Functional classifications were assigned to these ESTs and genes, potentially involved in the aflatoxin contamination process, were identified. Based on this EST sequence information, a genomic DNA amplicon microarray was constructed at The Institute for Genomic Research (TIGR). To identify potential regulatory networks controlling aflatoxin contamination in food and feeds, gene expression profiles in aflatoxin-supportive media versus non-aflatoxin-supportive media were evaluated in A. flavus and A. parasiticus. Genes consistently expressed in several aflatoxin-supportive media are reported.

摘要

黄曲霉毒素是由某些真菌物种产生的有毒且致癌的聚酮化合物代谢产物,包括黄曲霉和寄生曲霉。许多内部和外部因素,如营养和环境,都会影响黄曲霉毒素的生物合成;因此,我们使用从在几种条件下收获的菌丝体构建的标准化cDNA表达文库中的表达序列标签(EST)分析了黄曲霉的转录组。从26,110个测序的cDNA克隆中总共鉴定出7218个独特的EST。对这些EST和基因进行了功能分类,并鉴定了可能参与黄曲霉毒素污染过程的基因。基于此EST序列信息,基因组研究所(TIGR)构建了基因组DNA扩增子微阵列。为了确定控制食品和饲料中黄曲霉毒素污染的潜在调控网络,评估了黄曲霉和寄生曲霉在支持黄曲霉毒素的培养基与不支持黄曲霉毒素的培养基中的基因表达谱。报道了在几种支持黄曲霉毒素的培养基中持续表达的基因。

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