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两种单端孢霉烯族毒素P450基因在轮枝镰孢菌中的异源表达。

Heterologous expression of two trichothecene P450 genes in Fusarium verticillioides.

作者信息

McCormick Susan P, Alexander Nancy J, Proctor Robert H

机构信息

Mycotoxin Research Unit, USDA, ARS, National Center for Agricultural Utilization Research, IL 61604-3902, USA.

出版信息

Can J Microbiol. 2006 Mar;52(3):220-6. doi: 10.1139/w05-124.

Abstract

Fusarium graminearum Z-3639 and F. sporotrichioides NRRL3299 produce the trichothecene mycotoxins 15-acetyldeoxynivalenol and T-2 toxin, respectively. These toxins differ in oxygenation at C-4, C-7, and C-8. In F. sporotrichioides, Tri1 (FsTri1) controls C-8 hydroxylation. To determine the function of an apparent F. graminearum Tri1 (FgTri1) homolog, both FsTri1 and FgTri1 genes were heterologously expressed in the trichothecene-nonproducing species F. verticillioides by fusing the Tri1 coding regions to the promoter of the fumonisin biosynthetic gene FUM8. FsTri1 and FgTri1 have been partially characterized by disruption analysis, and the results from these analyses suggest that FsTri1 most likely has a single function but that FgTri1 may have two functions. Transgenic F. verticillioides carrying the FsTri1 (FvF8FsTri1) converted exogenous isotrichodermin and calonectrin to 8-hydroxyisotrichodermin and 8-hydroxycalonectrin, respectively. Transgenic F. verticillioides carrying FgTri1 (FvF8FgTri1) converted isotrichodermin to a mixture of 7-hydroxyisotrichodermin and 8-hydroxyisotrichodermin but converted calonectrin to a mixture of 7-hydroxycalonectrin, 8-hydroxycalonectrin, and 3,15-diacetyldeoxynivalenol. A fourth compound, 7,8-dihydroxycalonectrin, was identified in large-scale F. verticillioides FvF8FgTri1 cultures fed isotrichodermin. Our results indicate that FgTri1 controls both C-7 and C-8 hydroxylation but that FsTri1 controls only C-8 hydroxylation. Our studies also demonstrate that F. verticillioides can metabolize some trichothecenes by adding an acetyl group to C-3 or by removing acetyl groups from C-4 or C-15. In addition, wild-type F. verticillioides can convert 7,8-dihydroxycalonectrin to 3,15-diacetyldeoxynivalenol.

摘要

禾谷镰刀菌Z - 3639和拟枝孢镰刀菌NRRL3299分别产生单端孢霉烯族霉菌毒素15 - 乙酰脱氧雪腐镰刀菌烯醇和T - 2毒素。这些毒素在C - 4、C - 7和C - 8位的氧化情况不同。在拟枝孢镰刀菌中,Tri1(FsTri1)控制C - 8位的羟基化。为了确定禾谷镰刀菌Tri1(FgTri1)同源物的功能,通过将Tri1编码区与伏马菌素生物合成基因FUM8的启动子融合,在不产生单端孢霉烯族毒素的轮枝镰孢菌中异源表达了FsTri1和FgTri1基因。通过缺失分析对FsTri1和FgTri1进行了部分表征,这些分析结果表明FsTri1很可能具有单一功能,而FgTri1可能具有两种功能。携带FsTri1的转基因轮枝镰孢菌(FvF8FsTri1)分别将外源异三孢菌素和卡劳内酯转化为8 - 羟基异三孢菌素和8 - 羟基卡劳内酯。携带FgTri1的转基因轮枝镰孢菌(FvF8FgTri1)将异三孢菌素转化为7 - 羟基异三孢菌素和8 - 羟基异三孢菌素的混合物,但将卡劳内酯转化为7 - 羟基卡劳内酯、8 - 羟基卡劳内酯和3,15 - 二乙酰脱氧雪腐镰刀菌烯醇的混合物。在大规模用异三孢菌素培养的轮枝镰孢菌FvF8FgTri1中鉴定出了第四种化合物7,8 - 二羟基卡劳内酯。我们的结果表明FgTri1控制C - 7和C - 8位的羟基化,而FsTri1仅控制C - 8位的羟基化。我们的研究还表明,轮枝镰孢菌可以通过在C - 3位添加一个乙酰基或从C - 4或C - 15位去除乙酰基来代谢一些单端孢霉烯族毒素。此外,野生型轮枝镰孢菌可以将7,8 - 二羟基卡劳内酯转化为3,15 - 二乙酰脱氧雪腐镰刀菌烯醇。

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