来自细粒曲霉的ABC转运蛋白在抗细胞毒剂和抗生素生产中的作用。

A C Andrade, J G Van Nistelrooy, R B Peery, P L Skatrud, M A De Waard
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引用次数: 107

摘要

本文报道了丝状真菌细粒曲霉(Aspergillus nidulans)中两个新的ABC转运蛋白编码基因atrC和atrD (ABC transporters C和D)的特征,为atrD参与多药转运和抗生素生产提供了证据。经BLAST分析,AtrCp和AtrDp的氨基酸序列与p糖蛋白簇的ABC转运蛋白具有高度同源性。AtrDp与Afu Mdr1p的氨基酸序列具有特别高的一致性,Afu Mdr1p是一种先前从人类烟状芽胞杆菌中鉴定出来的ABC转运蛋白。Northern分析表明,在使用天然有毒化合物和外源药物处理真菌胚芽后,atrC和atrD的转录水平增加。atrC基因相对于attrD具有较高的组成表达水平,这表明它参与了代谢功能。利用稻瘟病菌pyrG作为选择性标记进行基因置换,产生了atrC和atrD的单敲除突变体。DeltatrD突变体对环己亚胺、环孢素衍生物PSC 833、尼日利亚菌素和valinomycin等化合物表现出过敏表型,表明AtrDp参与了对细胞毒性化合物的保护。唑类杀菌剂fenarimol的能量依赖性外排被AtrDp底物(如PSC 833、尼日利亚菌素和valinomycin)抑制,表明AtrDp在该杀菌剂的外排中起作用。最有趣的是,(delta)atrD突变体显示青霉素产量减少,间接测量为对黄体微球菌的抗菌活性。这些结果提示ABC转运蛋白可能参与真菌细胞分泌青霉素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role of ABC transporters from Aspergillus nidulans in protection against cytotoxic agents and in antibiotic production.

This paper describes the characterization of atrC and atrD (ABC transporters C and D), two novel ABC transporter-encoding genes from the filamentous fungus Aspergillus nidulans, and provides evidence for the involvement of atrD in multidrug transport and antibiotic production. BLAST analysis of the deduced amino acid sequences of AtrCp and AtrDp reveals high homology to ABC transporter proteins of the P-glycoprotein cluster. AtrDp shows a particularly high degree of identity to the amino acid sequence of Afu Mdr1p, a previously characterized ABC transporter from the human pathogen A. fumigatus. Northern analysis demonstrates an increase in transcript levels of atrC and atrD in fungal germlings upon treatment with natural toxic compounds and xenobiotics. The atrC gene has a high constitutive level of expression relative to attrD, which suggests its involvement in a metabolic function. Single knock-out mutants for atrC and atrD were generated by gene replacement using pyrG from A. oryzae as a selectable marker. DeltatrD mutants display a hypersensitive phenotype to compounds such as cycloheximide, the cyclosporin derivative PSC 833, nigericin and valinomycin, indicating that AtrDp is involved in protection against cytotoxic compounds. Energy-dependent efflux of the azole-related fungicide fenarimol is inhibited by substrates of AtrDp (e.g. PSC 833, nigericin and valinomycin), suggesting that AtrDp plays a role in efflux of this fungicide. Most interestingly, (delta)atrD mutants display a decrease in penicillin production, measured indirectly as antimicrobial activity against Micrococcus luteus. These results suggest that ABC transporters may be involved in secretion of penicillin from fungal cells.

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