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寄生曲霉黄曲霉毒素基因簇的物理和转录图谱以及黄曲霉毒素途径早期相关基因的功能破坏。

Physical and transcriptional map of an aflatoxin gene cluster in Aspergillus parasiticus and functional disruption of a gene involved early in the aflatoxin pathway.

作者信息

Trail F, Mahanti N, Rarick M, Mehigh R, Liang S H, Zhou R, Linz J E

机构信息

Department of Food Science and Human Nutrition, Michigan State University, East Lansing 48824, USA.

出版信息

Appl Environ Microbiol. 1995 Jul;61(7):2665-73. doi: 10.1128/aem.61.7.2665-2673.1995.

Abstract

Two genes involved in aflatoxin B1 (AFB1) biosynthesis in Aspergillus parasiticus, nor-1 and ver-1, were localized to a 35-kb region on one A. parasiticus chromosome and to the genomic DNA fragment carried on a single cosmid, NorA. A physical and transcriptional map of the 35-kb genomic DNA insert in cosmid NorA was prepared to help determine whether other genes located in the nor-1-ver-1 region were involved in aflatoxin synthesis. Northern (RNA) analysis performed on RNA isolated from A. parasiticus SU1 grown in aflatoxin-inducing medium localized 14 RNA transcripts encoded by this region. Eight of these transcripts, previously unidentified, showed a pattern of accumulation similar to that of nor-1 and ver-1, suggesting possible involvement in AFB1 synthesis. To directly test this hypothesis, gene-1, encoding one of the eight transcripts, was disrupted in A. parasiticus CS10, which accumulates the aflatoxin precursor versicolorin A, by insertion of plasmid pAPNVES4. Thin-layer chromatography revealed that gene-1 disruptant clones no longer accumulated versicolorin A. Southern hybridization analysis of these clones indicated that gene-1 had been disrupted by insertion of the disruption vector. These data confirmed that gene-1 is directly involved in AFB1 synthesis. The predicted amino acid sequence of two regions of gene-1 showed a high degree of identity and similarity with the beta-ketoacyl-synthase and acyltransferase functional domains of polyketide synthases, consistent with a proposed role for gene-1 in polyketide backbone synthesis.

摘要

寄生曲霉中参与黄曲霉毒素B1(AFB1)生物合成的两个基因,nor-1和ver-1,定位于寄生曲霉一条染色体上的一个35 kb区域以及一个单一黏粒NorA所携带的基因组DNA片段上。制备了黏粒NorA中35 kb基因组DNA插入片段的物理和转录图谱,以帮助确定位于nor-1-ver-1区域的其他基因是否参与黄曲霉毒素合成。对从在黄曲霉毒素诱导培养基中生长的寄生曲霉SU1分离的RNA进行的Northern(RNA)分析定位了该区域编码的14个RNA转录本。其中8个转录本此前未被鉴定,其积累模式与nor-1和ver-1相似,表明可能参与AFB1合成。为了直接验证这一假设,通过插入质粒pAPNVES4,在积累黄曲霉毒素前体杂色曲霉素A的寄生曲霉CS10中破坏了编码这8个转录本之一的gene-1。薄层色谱显示,gene-1破坏克隆不再积累杂色曲霉素A。对这些克隆的Southern杂交分析表明,gene-1已被破坏载体的插入所破坏。这些数据证实gene-1直接参与AFB1合成。gene-1两个区域的预测氨基酸序列与聚酮合酶的β-酮酰基合成酶和酰基转移酶功能域具有高度的同一性和相似性,这与gene-1在聚酮骨架合成中的假定作用一致。

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