Cloning and heterologous transcription of a polyketide synthase gene from the lichen Solorina crocea

被引:34
作者
Gagunashvili, Andrey N. [1 ]
Davidsson, Snorri P. [1 ]
Jonsson, Zophonias O. [1 ]
Andresson, Olafur S. [1 ]
机构
[1] Univ Iceland, Inst Biol, IS-101 Reykjavik, Iceland
来源
MYCOLOGICAL RESEARCH | 2009年 / 113卷
关键词
Lichen; Polyketides; Polyketide synthases; Secondary metabolites; 6-METHYLSALICYLIC ACID SYNTHASE; ASPERGILLUS-NIDULANS; AFLATOXIN BIOSYNTHESIS; MOLECULAR-CLONING; EXPRESSION; CLUSTER; FUNGI; TRANSFORMATION; PARASITICUS; METABOLITES;
D O I
10.1016/j.mycres.2008.11.011
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Lichens and most ascomycete fungi produce polyketide secondary metabolites often with valuable biological activities. Their biosynthesis is primarily governed by large iterative multifunctional type I polyketide synthases. Although there has been good progress studying filamentous non-lichenized fungi, there is limited information on polyketide biosynthesis in lichens and their mycobionts, due to their slow growth, difficulties in establishing pure cultures, and the absence of methods for direct genetic manipulation. However, heterologous expression in a surrogate host offers an alternative approach for exploring lichen polyketide biosynthesis. Here, we report cloning of a type I polyketide synthase gene from the foliose lichen Solorina crocea and its heterologous transcription in the filamentous fungus Aspergillus oryzae, including processing of the transcript. No new polyketide product was detected. The lichen polyketide synthase showed greatest homology with uncharacterized genes from filamentous fungi and lower homology with proteins catalysing biosynthesis of the decaketide alternapyrone and the tetraketide side-chain of squalestatin. The technology platform utilized here presents a useful tool for functional characterization of fungal biosynthetic genes and provides a means for novel production of valuable compounds. (c) 2008 The British Mycological Society. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:354 / 363
页数:10
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