藤黑赤霉素交配种群A产生b系列伏马菌素的生物合成及遗传关系。

R H Proctor, A E Desjardins, R D Plattner
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引用次数: 23

摘要

伏马菌素是由玉米病原菌藤黑赤霉素交配种群A产生的真菌毒素,经常污染玉米。野生型fujikuroi产生四种b系列伏马菌素,FB1, FB2, FR3和FB4。这些毒素除了沿其线性碳主链的羟基数目和位置不同外,在结构上是相同的。为了阐明这些伏马菌素之间的遗传和生物合成关系,我们对fujikuroi G.突变体进行了减数分裂和生化分析,这些突变体由于Fum1、Fum2和Fum3三个位点的等位基因缺陷而导致伏马菌素产生改变。这些突变体要么不产生伏马菌素,要么只产生FR2和FB4,要么只产生FR3和FR4。遗传分析显示真菌的真菌位点沿连锁群1的方向。这些突变体以成对组合的方式生长在一起,以确定它们的伏马菌素生产表型是否可以互补。当产生FR3-和fb2的突变体一起生长时,发生了互补。然而,当一个不产生FR2-或fb3的突变体与产生FR2-或fb3的突变体一起生长时,互补没有发生或不完全。当纯化的FR2、FR3或FB4被喂给突变培养物时,FR4主要转化为FR2, FR3转化为FB1, FB2不转化。这些检测结果提示伏马菌素生物合成途径中存在一个以前未被认识的分支。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biosynthetic and genetic relationships of B-series fumonisins produced by Gibberella fujikuroi mating population A.

Fumonisins are mycotoxins produced by the maize pathogen Gibberella fujikuroi mating population A and frequently contaminate maize. Wild-type G. fujikuroi produces four B-series fumonisins, FB1, FB2, FR3 and FB4. These toxins are identical in structure except for the number and positions of hydroxyls along their linear carbon backbone. To elucidate the genetic and biosynthetic relationships among these fumonisins, we conducted meiotic and biochemical analyses of G. fujikuroi mutants with altered fumonisin production that resulted from defective alleles at three loci, Fum1, Fum2 and Fum3. These mutants produced either no fumonisins, only FR2 and FB4, or only FR3 and FR4. Genetic analyses revealed the orientation of the Fum loci along linkage group 1 of the fungus. The mutants were grown together in pair-wise combinations to determine if their fumonisin production phenotypes could be complemented. When FR3- and FB2-producing mutants were grown together, complementation occurred. However, when a nonproducing mutant was grown with a FR2- or FB3-producing mutant, complementation did not occur or was incomplete. When purified FR2, FR3, or FB4 was fed to mutant cultures, FR4 was converted primarily to FR2, FR3 was converted to FB1 and FB2 was not converted. The results from these assays suggest a previously unrecognized branch in the fumonisin biosynthetic pathway.

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