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1
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2
Characterization of the function of the ver-1A and ver-1B genes, involved in aflatoxin biosynthesis in Aspergillus parasiticus.寄生曲霉中参与黄曲霉毒素生物合成的ver-1A和ver-1B基因功能的表征。
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3
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4
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本文引用的文献

1
Purification and characterization of two versiconal hemiacetal acetate reductases involved in aflatoxin biosynthesis.纯化和表征两种参与黄曲霉毒素生物合成的 versiconal 半缩醛乙酸酯还原酶。
Appl Environ Microbiol. 1994 Jul;60(7):2561-7. doi: 10.1128/aem.60.7.2561-2567.1994.
2
Regulated expression of the nor-1 and ver-1 genes associated with aflatoxin biosynthesis.与黄曲霉毒素生物合成相关的nor-1和ver-1基因的调控表达。
Appl Environ Microbiol. 1993 May;59(5):1642-6. doi: 10.1128/aem.59.5.1642-1646.1993.
3
Cloning of the afl-2 gene involved in aflatoxin biosynthesis from Aspergillus flavus.从黄曲霉中克隆参与黄曲霉毒素生物合成的afl-2基因。
Appl Environ Microbiol. 1993 Jan;59(1):156-62. doi: 10.1128/aem.59.1.156-162.1993.
4
Purification of a 40-kilodalton methyltransferase active in the aflatoxin biosynthetic pathway.纯化在黄曲霉毒素生物合成途径中具有活性的一种40千道尔顿甲基转移酶。
Appl Environ Microbiol. 1993 Feb;59(2):479-84. doi: 10.1128/aem.59.2.479-484.1993.
5
Gene cluster involved in melanin biosynthesis of the filamentous fungus Alternaria alternata.参与丝状真菌链格孢黑色素生物合成的基因簇。
J Bacteriol. 1993 Jul;175(14):4427-35. doi: 10.1128/jb.175.14.4427-4435.1993.
6
Stereochemistry during aflatoxin biosynthesis: conversion of norsolorinic acid to averufin.黄曲霉毒素生物合成过程中的立体化学:诺索尔菌素酸向阿弗菌素的转化。
Appl Environ Microbiol. 1993 Aug;59(8):2486-92. doi: 10.1128/aem.59.8.2486-2492.1993.
7
Cloning and characterization of a cDNA from Aspergillus parasiticus encoding an O-methyltransferase involved in aflatoxin biosynthesis.寄生曲霉中一个编码参与黄曲霉毒素生物合成的O-甲基转移酶的cDNA的克隆与特性分析
Appl Environ Microbiol. 1993 Nov;59(11):3564-71. doi: 10.1128/aem.59.11.3564-3571.1993.
8
Evidence for a gene cluster involving trichothecene-pathway biosynthetic genes in Fusarium sporotrichioides.在拟枝孢镰刀菌中涉及单端孢霉烯途径生物合成基因的基因簇的证据。
Curr Genet. 1993 Oct;24(4):291-5. doi: 10.1007/BF00336778.
9
Cloning of the Aspergillus parasiticus apa-2 gene associated with the regulation of aflatoxin biosynthesis.寄生曲霉中与黄曲霉毒素生物合成调控相关的apa-2基因的克隆
Appl Environ Microbiol. 1993 Oct;59(10):3273-9. doi: 10.1128/aem.59.10.3273-3279.1993.
10
Characterisation of a Streptomyces antibioticus gene encoding a type I polyketide synthase which has an unusual coding sequence.一种编码具有异常编码序列的I型聚酮合酶的抗生链霉菌基因的表征。
Mol Gen Genet. 1994 Feb;242(3):358-62. doi: 10.1007/BF00280426.

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.

DOI:10.1128/aem.61.7.2665-2673.1995
PMID:7618880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC167540/
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。