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首页> 外文期刊>Current Genetics >Impact of the cross-pathway control on the regulation of lysine and penicillin biosynthesis in Aspergillus nidulans
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Impact of the cross-pathway control on the regulation of lysine and penicillin biosynthesis in Aspergillus nidulans

机译:交叉途径控制对构巢曲霉赖氨酸和青霉素生物合成调控的影响

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摘要

The non-proteinogenic amino acid, α-aminoadipate, defines the biosynthetic branch-point of lysine and penicillin biosynthesis in the filamentous fungus, Aspergillus nidulans. Regulation of both pathways was analysed in response to amino acid limitation. The lysF-encoded homoaconitase acts upstream of the α-aminoadipate branch point, whereas the lysA gene product, saccharopine dehydrogenase, catalyses the ultimate step of the lysine-specific branch. The lysA gene from A. nidulans was identified and isolated. Amino acid starvation resulted in significantly increased transcription of lysA but not lysF. Starvation-dependent changes in transcription levels of lysA were dependent on the presence of the central transcriptional activator of the cross-pathway control (CPCA). The effect of amino acid starvation under penicillin-producing conditions was analysed in A. nidulans strains with reporter genes for the penicillin-biosynthesis genes, acvA and ipnA, and genetically altered activity of the cross-pathway control. Overproduction of CPCA decreased expression of ipnA and acvA reporter genes and even more drastically reduced penicillin production. This work suggests that, upon amino acid starvation, the cross-pathway control overrules secondary metabolite biosynthesis and favours the metabolic flux towards amino acids instead of penicillin in A. nidulans.
机译:非蛋白质氨基酸α-氨基己二酸定义丝状真菌构巢曲霉中赖氨酸和青霉素生物合成的生物合成分支点。响应氨基酸限制,分析了两种途径的调节。 lysF编码的均质硝酸酶在α-氨基己二酸分支点的上游起作用,而lysA基因产物糖荚果脱氢酶则催化赖氨酸特异性分支的最终步骤。鉴定并分离了来自构巢曲霉的lysA基因。氨基酸饥饿导致lysA的转录显着增加,但lysF却没有。饥饿依赖的lysA转录水平的变化取决于交叉通路对照(CPCA)中央转录激活因子的存在。在带有青霉素生物合成基因,acvA和ipnA的报告基因以及交叉途径控制的基因改变活性的报告基因A. nidulans菌株中,分析了青霉素生产条件下氨基酸饥饿的影响。 CPCA的过量生产会降低ipnA和acvA报告基因的表达,甚至会大大降低青霉素的产量。这项工作表明,在氨基酸饥饿时,交叉途径控制会否定次级代谢产物的生物合成,并有利于构巢曲霉中向氨基酸的代谢通量而不是青霉素的通量。

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  • 来源
    《Current Genetics》 |2003年第4期|209-219|共11页
  • 作者单位

    Institut für Mikrobiologie und Genetik Georg-August-Universität Grisebachstrasse 8 37077 Göttingen Germany;

    Institut für Mikrobiologie und Genetik Georg-August-Universität Grisebachstrasse 8 37077 Göttingen Germany;

    Institut für Mikrobiologie Universität Hannover Schneiderberg 50 30167 Hannover Germany;

    Institut für Mikrobiologie und Genetik Georg-August-Universität Grisebachstrasse 8 37077 Göttingen Germany;

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