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Strategy for efficient cloning of biosynthetic gene clusters from fungi

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Abstract

Filamentous fungi are excellent sources for the production of a group of bioactive small molecules which are often called secondary metabolites (SMs). The advanced genome sequencing technology combined with bioinformatics analysis reveals a large number of unexplored biosynthetic gene clusters (BGCs) in the fungal genomes. To unlock this fungal SM treasure, many approaches including heterologous expression are being developed and efficient cloning of the BGCs is a crucial step to do this. Here, we present an efficient strategy for the direct cloning of fungal BGCs. This strategy consisted of Splicing by Overlapping Extension (SOE)-PCR and yeast assembly in vivo. By testing 14 BGCs DNA fragments ranging from 7 kb to 52 kb, the average positive rate was over 80%. The maximal insertion size for fungal BGC assembly was 52 kb. Those constructs could be used conveniently for the heterologous expression leading to the discovery of novel natural products. Thus, our results provide an efficient and quick method for the low cost direct cloning of fungal BGCs.

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Correspondence to Wen-Bing Yin, Peng Zhang or Xing-Zhong Liu.

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Supporting Information

Table S1 SOE-PCR reaction system for obtaining the overlapping fragments

Table S2 Yeast transformation protocol

Table S3 Yeast colony PCR reaction

The supporting information is available online at http://life.scichina.com and https://link.springer.com. The supporting materials are published as submitted, without typesetting or editing. The responsibility for scientific accuracy and content remains entirely with the authors.

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Li, R., Li, Z., Ma, K. et al. Strategy for efficient cloning of biosynthetic gene clusters from fungi. Sci. China Life Sci. 62, 1087–1095 (2019). https://doi.org/10.1007/s11427-018-9511-7

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