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外生菌根中的碳分配:毒蝇伞单糖转运蛋白的鉴定与表达分析

Carbon allocation in ectomycorrhizas: identification and expression analysis of an Amanita muscaria monosaccharide transporter.

作者信息

Nehls U, Wiese J, Guttenberger M, Hampp R

机构信息

Universität Tübingen, Germany.

出版信息

Mol Plant Microbe Interact. 1998 Mar;11(3):167-76. doi: 10.1094/MPMI.1998.11.3.167.

Abstract

Ectomycorrhizas are formed between certain soil fungi and fine roots of predominantly woody plants. An important feature of this symbiosis is the supply of plant-derived carbohydrates to the fungus. As a first step toward a better understanding of the molecular basis of this process, we cloned a monosaccharide transporter from the ectomycorrhizal fungus Amanita muscaria. Degenerate oligonucleotide primers were designed to match conserved regions from known fungal sugar transporters. A cDNA fragment of the transporter was obtained from mycorrhizal mRNA by reverse transcription-polymerase chain reaction. This fragment was used to identify a clone (AmMst1) encoding the entire monosaccharide transporter in a Picea abies/A. muscaria mycorrhizal cDNA library. The cDNA codes for an open reading frame of 520 amino acids, showing best homology to a Neurospora crassa monosaccharide transporter. The function of AmMST1 as monosaccharide transporter was confirmed by heterologous expression of the cDNA in a Schizosaccharomyces pombe mutant lacking a monosaccharide uptake system. AmMst1 was constitutively expressed in fungal hyphae under all growth conditions. Nevertheless, in mycorrhizas as well as in hyphae grown at monosaccharide concentrations above 5 mM, the amount of AmMst1 transcript increased fourfold. We therefore suggest that AmMst1 is upregulated in ectomycorrhizas by a monosaccharide-controlled mechanism.

摘要

外生菌根是由某些土壤真菌与主要为木本植物的细根形成的。这种共生关系的一个重要特征是植物衍生的碳水化合物向真菌的供应。作为更好地理解这一过程分子基础的第一步,我们从外生菌根真菌毒蝇鹅膏中克隆了一种单糖转运蛋白。设计简并寡核苷酸引物以匹配已知真菌糖转运蛋白的保守区域。通过逆转录 - 聚合酶链反应从菌根mRNA中获得了转运蛋白的cDNA片段。该片段用于在挪威云杉/毒蝇鹅膏菌根cDNA文库中鉴定编码整个单糖转运蛋白的克隆(AmMst1)。该cDNA编码一个520个氨基酸的开放阅读框,与粗糙脉孢菌单糖转运蛋白具有最高的同源性。通过在缺乏单糖摄取系统的粟酒裂殖酵母突变体中对cDNA进行异源表达,证实了AmMST1作为单糖转运蛋白的功能。AmMst1在所有生长条件下在真菌菌丝中组成性表达。然而,在菌根以及在单糖浓度高于5 mM的条件下生长的菌丝中,AmMst1转录本的量增加了四倍。因此,我们认为AmMst1在外生菌根中通过单糖控制机制上调。

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